183 results on '"Rocha AJ"'
Search Results
2. Checklist Prisma
- Author
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Soares, JMS, Rocha, AJ, Nascimento, FS, Santos, AS, Miller, RNG, Ferreira, CF, Haddad, F, Amorim, VBO, and Amorim, EP
- Abstract
Checklist Prisma
- Published
- 2021
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3. Genetic improvement for resistance to Black Sigatoka in banana: a systematic review
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Soares, JMS, Rocha, AJ, Nascimento, FS, Santos, AS, Miller, RNG, Ferreira, CF, Haddad, F, Amorim, VBO, and Amorim, EP
- Subjects
Musa spp., Mycosphaerella fijiensis, genetic resistance, state-of-the-art - Abstract
Articles used for systematic review on the genetic improvement of bananas with a focus on black Sigatoka during the last ten years.
- Published
- 2021
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4. Supplementary Materials
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Rocha, AJ, Soares, JMS, Nascimento, FS, Santos, AS, Amorim, VBO, Mizubuti, ESG, Ferreira, CF, Haddad, F, and Amorim, EP
- Abstract
Supplementary Materials
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- 2020
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5. Erratum: Atypical idiopathic inflammatory demyelinating lesions: Prognostic implications and relation to multiple sclerosis (Journal of Neurology (2013) 260 (2016-2022) DOI: 10.1007/s00415-013-6918-y)
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Wallner-Blazek, M, Rovira, A, Filippi, M, Rocca, MA, Miller, DH, Schmierer, K, Frederiksen, J, Gass, A, Gama, H, Tilbery, CP, Rocha, AJ, Flores, J, Barkhof, F, Seewann, A, Palace, J, Yousry, T, Montalban, X, Enzinger, C, and Fazekas, F
- Published
- 2016
6. A case review of the MRI features in alternating Tolosa–Hunt syndrome
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Guedes, BVS, primary, da Rocha, AJ, additional, Zuppani, HB, additional, da Silva, CJ, additional, and Sanvito, WL, additional
- Published
- 2010
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7. Paroxysmal Hemicrania-Tic and Chiari I Malformation: An Unusual Association
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Monzillo, P, primary, Nemoto, P, additional, Costa, A, additional, and Rocha, AJ, additional
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- 2007
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8. Lipomyelocele with osseous dysraphic hamartoma in a child: a case report.
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Zuppani HB, Guedes Bde V, da Silva CJ, and da Rocha AJ
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- 2010
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9. Teaching NeuroImages: isolated hypothalamic hamartoma vs Pallister-Hall syndrome: imaging and clinical correlation.
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da Rocha AJ, Rosa Junior M, Arita FN, Nita DA, da Rocha, Antonio J, Rosa Junior, Marcos, Arita, Fernando Norio, and Nita, Dragos A
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- 2012
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10. Implications of early staples removal at cesarean delivery.
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Rocha AJ, Rodrigues T, and Neves JP
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- 2011
11. Cognitive and olfactory deficits in Machado-Joseph disease: A dopamine transporter study.
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Braga-Neto P, Felicio AC, Hoexter MQ, Pedroso JL, Dutra LA, Alessi H, Minett T, Santos-Galduroz RF, da Rocha AJ, Garcia LA, Bertolucci PH, Bressan RA, and Barsottini OG
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- 2012
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12. Atypical idiopathic inflammatory demyelinating lesions: prognostic implications and relation to multiple sclerosis
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Klaus Schmierer, M Wallner-Blazek, Frederik Barkhof, Charles Peter Tilbery, Hugo Pereira Pinto Gama, Tarek A. Yousry, José Flores, Christian Enzinger, Massimo Fillipp, Xavier Montalban, Jette L. Frederiksen, Alex Rovira, Antônio José da Rocha, Jacqueline Palace, David Miller, M A Rocca, Alexandra Seewann, Franz Fazekas, Achim Gass, Radiology and nuclear medicine, Neurology, NCA - Neuroinflamation, Wallner Blazek, M, Rovira, A, Filippi, Massimo, Rocca, Ma, Miller, Dh, Schmierer, K, Frederiksen, J, Gass, A, Gama, H, Tilbery, Cp, Rocha, Aj, Florez, J, Barkhof, F, Seewann, A, Palace, J, Yousry, Ta, Montalban, X, Enzinger, C, Fazekas, F, and on behalf of the MAGNIMS, Group
- Subjects
Adult ,Male ,medicine.medical_specialty ,Pathology ,Multiple Sclerosis ,Neurology ,Adolescent ,Databases, Factual ,Gastroenterology ,Lesion ,Young Adult ,Sex Factors ,Internal medicine ,medicine ,Humans ,Young adult ,Neuroradiology ,medicine.diagnostic_test ,business.industry ,Multiple sclerosis ,Age Factors ,Clinical course ,Brain ,Magnetic resonance imaging ,Polyradiculoneuropathy ,Middle Aged ,Prognosis ,medicine.disease ,Magnetic Resonance Imaging ,Polyradiculoneuropathy, Chronic Inflammatory Demyelinating ,Disease Progression ,Female ,Neurology (clinical) ,medicine.symptom ,business ,Follow-Up Studies - Abstract
Atypical lesions of a presumably idiopathic inflammatory demyelinating origin present quite variably and may pose diagnostic problems. The subsequent clinical course is also uncertain. We, therefore, wanted to clarify if atypical idiopathic inflammatory demyelinating lesions (AIIDLs) can be classified according to previously suggested radiologic characteristics and how this classification relates to prognosis. Searching the databases of eight tertiary referral centres we identified 90 adult patients (61 women, 29 men; mean age 34 years) with ≥1 AIIDL. We collected their demographic, clinical and magnetic resonance imaging data and obtained follow-up (FU) information on 77 of these patients over a mean duration of 4 years. The AIIDLs presented as a single lesion in 72 (80 %) patients and exhibited an infiltrative (n = 35), megacystic (n = 16), Baló (n = 10) or ring-like (n = 16) lesion appearance in 77 (86 %) patients. Additional multiple sclerosis (MS)-typical lesions existed in 48 (53 %) patients. During FU, a further clinical attack occurred rarely (23-35 % of patients) except for patients with ring-like AIIDLs (62 %). Further attacks were also significantly more often in patients with coexisting MS-typical lesions (41 vs. 10 %, p < 0.005). New AIIDLs developed in six (7 %), and new MS-typical lesions in 29 (42 %) patients. Our findings confirm the previously reported subtypes of AIIDLs. Most types confer a relatively low risk of further clinical attacks, except for ring-like lesions and the combination with MS-typical lesions. © 2013 Springer-Verlag Berlin Heidelberg.
- Published
- 2013
13. Use of CRISPR Technology in Gene Editing for Tolerance to Biotic Factors in Plants: A Systematic Review.
- Author
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Mascarenhas MS, Nascimento FDS, Rocha AJ, Ferreira MDS, Oliveira WDDS, Morais Lino LS, Mendes TAO, Ferreira CF, Santos-Serejo JAD, and Amorim EP
- Abstract
The objective of this systematic review (SR) was to select studies on the use of gene editing by CRISPR technology related to plant resistance to biotic stresses. We sought to evaluate articles deposited in six electronic databases, using pre-defined inclusion and exclusion criteria. This SR demonstrates that countries such as China and the United States of America stand out in studies with CRISPR/Cas. Among the most studied crops are rice, tomatoes and the model plant Arabidopsis thaliana . The most cited biotic agents include the genera, Xanthomonas, Manaporthe, Pseudomonas and Phytophthora . This SR also identifies several CRISPR/Cas-edited genes and demonstrates that plant responses to stressors are mediated by many complex signaling pathways. The Cas9 enzyme is used in most articles and Cas12 and 13 are used as additional editing tools. Furthermore, the quality of the articles included in this SR was validated by a risk of bias analysis. The information collected in this SR helps to understand the state of the art of CRISPR/Cas aimed at improving resistance to diseases and pests to understand the mechanisms involved in most host-pathogen relationships. This SR shows that the CRISPR/Cas system provides a straightforward method for rapid gene targeting, providing useful information for plant breeding programs.
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- 2024
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14. Joubert syndrome with the decaying molar tooth sign: report of 2 cases.
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Scortegagna F, Corrêa DG, Pacheco FT, Nunes RH, and da Rocha AJ
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- 2024
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15. Trio-based whole exome sequencing in patients with ectopic posterior pituitary.
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Lyra A, Rodart IF, Barros L, Silva TSE, da Rocha AJ, Kochi C, and Longui CA
- Abstract
Introduction: Ectopic posterior pituitary (EPP) is a rare congenital abnormality, sometimes associated with other midline defects, such as pituitary stalk interruption syndrome (PSIS), in which thin or absent pituitary stalk and anterior pituitary hypoplasia are combined to EPP. Most cases are sporadic, with few reports of familial cases, and many congenital hypopituitarism (CH) cases remain unsolved., Objective: To search for candidate genes associated with this condition, we performed trio-based whole-exome sequencing (WES) on patients with EPP, including two familial cases., Methods: This study included subjects with EPP and PSIS diagnosed by a simple MRI protocol (FAST1.2). We performed two distinct analyses in the trio-based WES. We looked for previously described genes associated with pituitary development. Next, we investigated the whole exome for variants inherited in a pattern consistent with a monogenic etiology., Results: Ten families were evaluated; eight were composed of a child with EPP and healthy parents, one has two affected siblings, and one family has a son and mother with EPP. When analyzing the previously described candidate variants associated with pituitary development, we found variants in GLI2 and FGFR1 in three families. We also found six other variants of interest in three patients: KMT2A , GALR3 , RTN4R , SEMA3A , NIPBL , and DSCAML1 ., Conclusion: The analysis allowed us to find previously reported and not reported GLI2 variants, all inherited from healthy parents, which reinforces the incomplete penetrance pattern of GLI2 variants in the development of EPP and draws attention to possible future functional studies of those variants that have a recurrent expression in CH. We also found novel FGFR1 and SEMA3A variants that suggest an oligogenic mechanism in PSIS and EPP, as seen in patients with hypogonadotropic hypogonadism. We report the first case of a patient with Wiedemann-Steiner syndrome and PSIS, suggesting that the KMT2A gene may be related to pituitary development. Furthermore, the trios' analysis allowed us to find five other variants of interest. Future investigations may clarify the roles of these variants in the etiology of EPP and PSIS., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (© 2024 Lyra, Rodart, Barros, Silva, da Rocha, Kochi and Longui.)
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- 2024
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16. Antiparasitic Evaluation of Aquiluscidin, a Cathelicidin Obtained from Crotalus aquilus , and the Vcn-23 Derivative Peptide against Babesia bovis , B. bigemina and B. ovata .
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Hernández-Arvizu EE, Asada M, Kawazu SI, Vega CA, Rodríguez-Torres A, Morales-García R, Pavón-Rocha AJ, León-Ávila G, Rivas-Santiago B, and Mosqueda J
- Abstract
Babesiosis is a growing concern due to the increased prevalence of this infectious disease caused by Babesia protozoan parasites, affecting various animals and humans. With rising worries over medication side effects and emerging drug resistance, there is a notable shift towards researching babesiacidal agents. Antimicrobial peptides, specifically cathelicidins known for their broad-spectrum activity and immunomodulatory functions, have emerged as potential candidates. Aquiluscidin, a cathelicidin from Crotalus aquilus , and its derivative Vcn-23, have been of interest due to their previously observed antibacterial effects and non-hemolytic activity. This work aimed to characterize the effect of these peptides against three Babesia species. Results showed Aquiluscidin's significant antimicrobial effects on Babesia species, reducing the B . bigemina growth rate and exhibiting IC
50 values of 14.48 and 20.70 μM against B . ovata and B . bovis , respectively. However, its efficacy was impacted by serum presence in culture, and it showed no inhibition against a B. bovis strain grown in serum-supplemented medium. Conversely, Vcn-23 did not demonstrate babesiacidal activity. In conclusion, Aquiluscidin shows antibabesia activity in vitro and its efficacy is affected by the presence of serum in the culture medium. Nevertheless, this peptide represents a candidate for further investigation of its antiparasitic properties and provides insights into potential alternatives for the treatment of babesiosis.- Published
- 2024
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17. Phytoparasitic Nematodes of Musa spp. with Emphasis on Sources of Genetic Resistance: A Systematic Review.
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Sousa ABP, Rocha AJ, Oliveira WDDS, Rocha LS, and Amorim EP
- Abstract
Bananas are a staple food that considerably contributes to both food security and income generation, especially in countries of Africa, Asia, and Central and South America. The banana plant ( Musa spp.) is affected by various pathogens, of main concern being the plant-parasitic nematodes associated with the rhizosphere, the most important of which are Radopholus similis (burrowing nematode), Helicotylenchus sp. (spiral nematode), Pratylenchus sp. (root lesion nematode), and Meloidogyne sp. (gall nematode). Infected plants reduce their ability to absorb water and nutrients, which can lead to delayed flowering, fewer bunches, and lower fruit mass. Obtaining nematode-resistant banana cultivars through genetic improvement is an effective and sustainable option compared with chemical control with nematicides. Here, we provide the first systematic review of existing banana sources of resistance to nematodes to aid the management and control of nematodes in banana and plantain crops. Articles selected from different databases were evaluated, and searches were conducted using pre-established inclusion and exclusion criteria. We found 69 studies dealing with genetic improvement for nematode resistance in banana cultivation. Our findings revealed that sources of resistance are currently under investigation to combat the diseases caused by different nematode species in banana plants.
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- 2024
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18. Neuroimaging of Infectious Vasculopathy.
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Nunes RH, Corrêa DG, Pacheco FT, Fonseca APA, Hygino da Cruz LC Jr, and da Rocha AJ
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- Humans, Cerebral Angiography, Neuroimaging, Communicable Diseases complications, Vasculitis complications, Vasculitis, Central Nervous System diagnostic imaging, Vasculitis, Central Nervous System complications
- Abstract
Vasculitis is a complication of several infectious diseases affecting the central nervous system, which may result in ischemic and/or hemorrhagic stroke, transient ischemic attack, and aneurysm formation. Infectious agents may directly infect the endothelium causing vasculitis or indirectly affect the vessel wall through an immunological cascade. Clinical manifestations usually overlap with those of noninfectious vascular diseases, making diagnosis challenging. Neuroimaging enables the identification of inflammatory changes in intracranial vasculitis. In this article, we review the imaging features of infectious vasculitis of bacterial, viral, fungal and parasitic causes., (Copyright © 2023 Elsevier Inc. All rights reserved.)
- Published
- 2024
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19. "Bunch of acai berries sign": a new radiological sign in patients with CNS involvement in Chagas disease.
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Fonseca APA, de Melo RFQ, Menezes T, Soares CMA, Rodrigues V, Alves RPM, Pincerato RCM, Roca F, and da Rocha AJ
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- Humans, Radiography, Euterpe parasitology, Chagas Disease diagnostic imaging, Chagas Disease epidemiology, Chagas Disease parasitology, Trypanosoma cruzi, Central Nervous System Neoplasms
- Abstract
Chagas disease is an infection caused by Trypanosoma cruzi, a parasite endemic in Latin America. Acute involvement of the CNS by Chagas has been considered rare, but presumed reactivation of chronic disease in immunosuppressed patients has been the subject of recent reports. Our objective is to describe the clinical and imaging characteristics of four patients with Chagas disease and CNS involvement, and the patients had to have available MRI and a diagnosis confirmed by biopsy. The imaging findings were similar, highlighting the presence of focal cerebral lesions with hypointensity on T2-WI, and these lesions assume a "bunch of acai berries appearance", a fruit involved in the transmission of T. cruzi. The post Gd T1-WI shows punctate enhancement. Knowledge of this pattern may be crucial to recognize this disease in immunocompromised patients from endemic areas., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2023
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20. Vascular Myelopathies.
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Padilha IG, Fonseca APA, Amancio CT, Vieira APF, Pacheco FT, and da Rocha AJ
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- Humans, Risk Factors, Vascular Diseases diagnostic imaging, Spinal Cord Diseases diagnostic imaging
- Abstract
There are many vascular disorders that can affect the spinal cord, and their prevalence and etiology are highly influenced by age, sex, and risk factors. This article reviews the embryology and anatomy of the spinal cord, as well as several vascular conditions, describing their clinical and imaging presentation, emphasizing the different imaging modalities' contributions to increasing specificity and better defining the most appropriate therapy strategy for improving the patient's prognosis., (Copyright © 2023 Elsevier Inc. All rights reserved.)
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- 2023
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21. Imaging Aspects of Toxic and Metabolic Myelopathies.
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Corrêa DG, da Cruz LCH Jr, da Rocha AJ, and Pacheco FT
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- Humans, Diagnostic Imaging, Spinal Cord Diseases diagnostic imaging, Spinal Cord Diseases etiology
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Metabolic and toxic myelopathies usually occurs due to several different causes. Metabolic myelopathy usually occurs due to deficiency of a nutrient, such as vitamin B12. Toxic myelopathy occurs secondary to the exposure to an external toxic agent. Although they may have a difficult diagnosis, determination of the specific cause of myelopathy is of utmost importance, because many causes are amenable to treatment. Although they have many clinical, electrophysiologic, and neuropathologic similarities, imaging may aid in the suspicion of toxic or metabolic myelopathy. The aim of this article, is to review the imaging features of the main toxic and metabolic myelopathies., (Copyright © 2023 Elsevier Inc. All rights reserved.)
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- 2023
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22. Mechanism of molecular interaction of sitagliptin with human DPP 4 enzyme - New Insights.
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Gonzatti MB, Júnior JEM, Rocha AJ, de Oliveira JS, Evangelista AJJ, Fonseca FMP, Ceccatto VM, de Oliveira AC, and da Cruz Freire JE
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- Humans, Sitagliptin Phosphate pharmacology, Molecular Docking Simulation, Hypoglycemic Agents pharmacology, Hypoglycemic Agents chemistry, Peptides, Dipeptidyl-Peptidase IV Inhibitors pharmacology, Dipeptidyl-Peptidase IV Inhibitors chemistry, Diabetes Mellitus, Type 2
- Abstract
Purpose: Dipeptidyl peptidase 4 (DPP
4 ) inactivates a range of bioactive peptides. The cleavage of insulinotropic peptides and glucagon-like peptide 1 (GLP1 ) by DPP4 directly influences glucose homeostasis. This study aimed to describe the mode of interaction between sitagliptin (an antidiabetic drug) and human DPP4 using in silico approaches., Materials and Methods: Docking studies were conducted using AutoDock Vina, 2D and 3D schematic drawings were obtained using PoseView and PLIP servers, and the DPP4 -sitagliptin complex was visualized with Pymol software., Results: The best affinity energy to form the DPP4 -sitagliptin complex was E-value = - 8.1 kcal mol-1 , as indicated by docking simulations. This result suggests a strong interaction. According to our observations, hydrophobic interactions involving the amino acids residues Tyr663 and Val712 , hydrogen bonds (Glu203 , Glu204 , Tyr663 , and Tyr667 ), π-Stacking interactions (Phe355 and Tyr667 ), and halogenic bonds (Arg123 , Glu204 , and Arg356 ) were prevalent in the DPP4 -sitagliptin complex. Root Mean Square Deviation prediction also demonstrated that the global structure of the human DPP4 did not have a significant change in its topology, even after the formation of the DPP4 -sitagliptin complex., Conclusion: The stable interaction between the sitagliptin ligand and the DPP4 enzyme was demonstrated through molecular docking simulations. The findings presented in this work enhance the understanding of the physicochemical properties of the sitagliptin interaction site, supporting the design of more efficient gliptin-like iDPP4 inhibitors., Competing Interests: Declaration of competing interest The authors declare no conflict of interests., (Copyright © 2023 Medical University of Bialystok. Published by Elsevier B.V. All rights reserved.)- Published
- 2023
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23. BAC Transgenic Expression of Human TREM2-R47H Remodels Amyloid Plaques but Unable to Reprogram Plaque-associated Microglial Reactivity in 5xFAD Mice.
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Lee CYD, De La Rocha AJ, Inouye K, Langfelder P, Daggett A, Gu X, Jiang LL, Pamonag Z, Vaca RG, Richman J, Kawaguchi R, Gao F, Xu H, and Yang XW
- Abstract
Background: Genetic study of late-onset Alzheimer's disease (AD) reveals that a rare Arginine-to-Histamine mutation at amino acid residue 47 (R47H) in Triggering Receptor Expressed on Myeloid Cells 2 (TREM2) results in increased disease risk. TREM2 plays critical roles in regulating microglial response to amyloid plaques in AD, leading to their clustering and activation surrounding the plaques. We previously showed that increasing human TREM2 gene dosage exerts neuroprotective effects against AD-related deficits in amyloid depositing mouse models of AD. However, the in vivo effects of the R47H mutation on human TREM2-mediated microglial reprogramming and neuroprotection remains poorly understood., Method: Here we created a BAC transgenic mouse model expressing human TREM2 with the R47H mutation in its cognate genomic context (BAC-TREM2-R47H). Importantly, the BAC used in this study was engineered to delete critical exons of other TREM-like genes on the BAC to prevent confounding effects of overexpressing multiple TREM-like genes. We crossed BAC-TREM2- R47H mice with 5xFAD [1], an amyloid depositing mouse model of AD, to evaluate amyloid pathologies and microglial phenotypes, transcriptomics and in situ expression of key TREM2 -dosage dependent genes. We also compared the key findings in 5xFAD/BAC-TREM2-R47H to those observed in 5xFAD/BAC-TREM2 mice., Result: Both BAC-TREM2 and BAC-TREM2-R47H showed proper expression of three splicing isoforms of TREM2 that are normally found in human. In 5xFAD background, elevated TREM2-R47H gene dosages significantly reduced the plaque burden, especially the filamentous type. The results were consistent with enhanced phagocytosis and altered NLRP3 inflammasome activation in BAC- TREM2-R47H microglia in vitro. However, unlike TREM2 overexpression, elevated TREM2- R47H in 5xFAD failed to ameliorate cognitive and transcriptomic deficits. In situ analysis of key TREM2 -dosage dependent genes and microglial morphology uncovered that TREM2-R47H showed a loss-of-function phenotype in reprogramming of plaque-associated microglial reactivity and gene expression in 5xFAD., Conclusion: Our study demonstrated that the AD-risk variant has a previously unknown, mixture of partial and full loss of TREM2 functions in modulating microglial response in AD mouse brains. Together, our new BAC-TREM2-R47H model and prior BAC-TREM2 mice are invaluable resource to facilitate the therapeutic discovery that target human TREM2 and its R47H variant to ameliorate AD and other neurodegenerative disorders.
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- 2023
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24. New reports of parasitism by Synhimantus (Dispharynx) nasuta (Rudolphi, 1819) (Nematoda: Acuariidae) in wild birds in Brazil.
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Severino AJM, Rocha AJ, Vieira FM, Muniz-Pereira LC, and Souza Lima S
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- Animals, Brazil, Nematoda anatomy & histology, Spirurida, Passeriformes parasitology, Falconiformes parasitology, Strigiformes
- Abstract
The aim of this study was to register the first occurrence of Synhimantus (Dispharynx) nasuta (Nematoda: Acuariidae) in some species of wild birds in Brazil. In addition, the aim was to deepen the knowledge about the morphology of this species through analysis using scanning electron microscopy. Nematodes were collected in wild birds of the species Turdus leucomelas, T. rufiventris, Mimus saturninus, Pitangus sulphuratus, Megascops choliba, Tyto furcata, and Falco sparverius. The morphological and morphometric data observed in the nematodes prove that these parasites are S. (D.) nasuta. This study also provides morphological data from light microscopy and scanning electron microscopy (SEM), as well as the morphometry of this nematode in each host species. Therefore, the current study confirms the first record of this nematode in F. sparverius and T. furcata in South America and, at the same time, these findings expand the host range of this parasite species worldwide, through the first records in M. choliba, M. saturninus, T. leucomelas and T. rufiventris.
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- 2023
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25. Intracranial vessel wall magnetic resonance imaging features of infectious vasculitis.
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Corrêa DG, Pacheco FT, da Cruz LCH Jr, Nunes RH, Maia ACM Jr, de Souza Godoy LF, Bisolo L, da Silva NA Jr, Soldatelli MD, de Siqueira Campos CM, Vedolin LM, do Amaral LLF, and da Rocha AJ
- Subjects
- Humans, Magnetic Resonance Angiography methods, Contrast Media, Cerebral Angiography methods, Gadolinium, Magnetic Resonance Imaging, Vasculitis, Central Nervous System diagnostic imaging, Vasculitis, Central Nervous System pathology, Communicable Diseases
- Abstract
Vasculitis is a complication of several infectious diseases affecting the central nervous system, which may result in ischemic and/or hemorrhagic stroke, transient ischemic attack, and aneurysm formation. The infectious agent may directly infect the endothelium, causing vasculitis, or indirectly affect the vessel wall through an immunological mechanism. The clinical manifestations of these complications usually overlap with those of non-infectious vascular diseases, making diagnosis challenging. Intracranial vessel wall magnetic resonance imaging (VWI) enables the evaluation of the vessel wall and the diseases that affect it, providing diagnostic data beyond luminal changes and enabling the identification of inflammatory changes in cerebral vasculitis. This technique demonstrates concentric vessel wall thickening and gadolinium enhancement, associated or not with adjacent brain parenchymal enhancement, in patients with vasculitis of any origin. It permits the detection of early alterations, even before a stenosis occurs. In this article, we review the intracranial vessel wall imaging features of infectious vasculitis of bacterial, viral, and fungal etiologies., Competing Interests: Declaration of competing interest None., (Copyright © 2023 Elsevier Inc. All rights reserved.)
- Published
- 2023
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26. Gene Editing for Plant Resistance to Abiotic Factors: A Systematic Review.
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Nascimento FDS, Rocha AJ, Soares JMDS, Mascarenhas MS, Ferreira MDS, Morais Lino LS, Ramos APS, Diniz LEC, Mendes TAO, Ferreira CF, Santos-Serejo JAD, and Amorim EP
- Abstract
Agricultural crops are exposed to various abiotic stresses, such as salinity, water deficits, temperature extremes, floods, radiation, and metal toxicity. To overcome these challenges, breeding programs seek to improve methods and techniques. Gene editing by Clustered Regularly Interspaced Short Palindromic Repeats-CRISPR/Cas-is a versatile tool for editing in all layers of the central dogma with focus on the development of cultivars of plants resistant or tolerant to multiple biotic or abiotic stresses. This systematic review (SR) brings new contributions to the study of the use of CRISPR/Cas in gene editing for tolerance to abiotic stress in plants. Articles deposited in different electronic databases, using a search string and predefined inclusion and exclusion criteria, were evaluated. This SR demonstrates that the CRISPR/Cas system has been applied to several plant species to promote tolerance to the main abiotic stresses. Among the most studied crops are rice and Arabidopsis thaliana , an important staple food for the population, and a model plant in genetics/biotechnology, respectively, and more recently tomato, whose number of studies has increased since 2021. Most studies were conducted in Asia, specifically in China. The Cas9 enzyme is used in most articles, and only Cas12a is used as an additional gene editing tool in plants. Ribonucleoproteins (RNPs) have emerged as a DNA-free strategy for genome editing without exogenous DNA. This SR also identifies several genes edited by CRISPR/Cas, and it also shows that plant responses to stress factors are mediated by many complex-signaling pathways. In addition, the quality of the articles included in this SR was validated by a risk of bias analysis. The information gathered in this SR helps to understand the current state of CRISPR/Cas in the editing of genes and noncoding sequences, which plays a key role in the regulation of various biological processes and the tolerance to multiple abiotic stresses, with potential for use in plant genetic improvement programs.
- Published
- 2023
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27. Arterial Spin Labeling: Techniques, Clinical Applications, and Interpretation.
- Author
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Iutaka T, de Freitas MB, Omar SS, Scortegagna FA, Nael K, Nunes RH, Pacheco FT, Maia Júnior ACM, do Amaral LLF, and da Rocha AJ
- Subjects
- Child, Humans, Spin Labels, Magnetic Resonance Imaging methods, Artifacts, Magnetic Resonance Angiography methods, Cerebrovascular Circulation physiology
- Abstract
Arterial spin labeling (ASL) is an emerging noninvasive MRI technique for assessing cerebral perfusion. An important advantage of ASL perfusion is the lack of a requirement for an exogenous tracer. ASL uses magnetically labeled water protons from arterial blood as an endogenous diffusible tracer. For this reason, ASL is an attractive perfusion imaging modality for children and for patients with contraindications or adverse reactions to gadolinium, patients with renal failure, and those who need repeated follow-up imaging. Another advantage of ASL is the possibility of quantifying cerebral blood flow, which provides an opportunity for comparative analysis among multiple longitudinal studies, unlike other MR perfusion techniques, which are semiquantitative and yield relative perfusion parameters. Advances in MRI technology and pulse sequence design have translated ASL beyond the research arena to successful clinical implementation. However, ASL is still underused in routine clinical practice. Some disadvantages of ASL include a lower signal-to-noise ratio and a longer acquisition time than those with dynamic susceptibility contrast-enhanced MRI. Additional factors limiting the use of ASL include variations in existing techniques and pulse sequence design, the complexity of implementation and postprocessing, insufficient experience with and/or knowledge of the potential clinical applications, and the absence of interpretation guidelines. The authors review the technical and physiologic basis of ASL perfusion, as well as artifacts, pitfalls, and its current clinical applications. A practical approach for interpreting ASL findings is also suggested., (© RSNA, 2022.)
- Published
- 2023
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28. Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation.
- Author
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Camelo CG, Artilheiro MC, Martins Moreno CA, Ferraciolli SF, Serafim Silva AM, Fernandes TR, Lucato LT, Rocha AJ, Reed UC, and Zanoteli E
- Subjects
- Humans, Brain diagnostic imaging, Genotype, Laminin genetics, Magnetic Resonance Imaging, Phenotype, Epilepsy diagnostic imaging, Epilepsy genetics, Intellectual Disability diagnostic imaging, Intellectual Disability genetics
- Abstract
Background: LAMA2-related muscular dystrophy is a disorder that causes muscle weakness and varies in severity, from a severe, congenital type to a milder, late-onset form. However, the disease does not only affect the muscles, but has systemic involvement and can lead to alterations such as brain malformation, epilepsy and intellectual disability., Objective: Describe the frequency of cortical malformations, epilepsy and intellectual disability in LAMA2-RD in a Brazilian cohort and correlate the neurological findings to genetic and motor function., Methods: This is an observational study of 52 LAMA2-RD patients, who were divided into motor function subgroups and compared based on brain MRI findings, epilepsy, intellectual disability, and type of variants and variant domains., Results: 44 patients (84.6%) were only able to sit, and 8 patients (15.4%) were able to walk. 10 patients (19.2%) presented with cortical malformations (polymicrogyria, lissencephaly-pachygyria, and cobblestone),10 patients (19.2%) presented with epilepsy, and 8 (15.4%) had intellectual disability. CNS manifestations correlated with a more severe motor phenotype and none of the patients able to walk presented with cortical malformation or epilepsy. There was a relation between gene variants affecting the laminin-α2 LG-domain and the presence of brain malformation (P = 0.016). There was also a relation between the presence of null variants and central nervous system involvement. A new brazilian possible founder variant was found in 11 patients (21,15%) (c.1255del; p. Ile419Leufs*4)., Conclusion: Cortical malformations, epilepsy and intellectual disability are more frequent among LAMA2-RD patients than previously reported and correlate with motor function severity and the presence of variants affecting the laminin-α2 LG domain. This brings more insight fore phenotype-genotype correlations, shows the importance of reviewing the brain MRI of patients with LAMA2-RD and allows greater attention to the risk of brain malformation, epilepsy, and intellectual disability in those patients with variants that affect the LG domain.
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- 2023
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29. Extra-pituitary midline structural abnormalities associated with ectopic posterior pituitary detected on a new rapid MRI protocol (FAST1.2).
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Lyra A, de Faria Guimarães D, Meira AS, Peixoto GV, Sousa E Silva T, Longui CA, Kochi C, and da Rocha AJ
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- Humans, Cross-Sectional Studies, Pituitary Gland diagnostic imaging, Magnetic Resonance Imaging methods, Hypopituitarism diagnostic imaging, Septo-Optic Dysplasia
- Abstract
Objective: Test if the MRI FAST1.2 protocol can detect extra-pituitary midline structural brain abnormalities in patients with ectopic posterior pituitary (EPP), and highlighting their radiological-laboratory correlations., Subjects and Methods: Cross-sectional study of patients with EPP and control group. All individuals were submitted to FAST1.2, which combines the FAST1 protocol developed by our group with 3D T2DRIVE imaging., Results: We evaluated 36 individuals with EPP and 78 as control group. Pituitary stalk (PS) was identified in 7/36 patients in EPP group by FAST1, and in 24/36 patients in FAST1.2 (p < 0.001). FAST1 failed to detect PS in one individual in the control group, while the FAST1.2 defined the PS in all individuals. In EPP group, eleven had interhypothalamic adhesion (IHA), three septo-optic dysplasia, and one cerebellar malformation. We didn't observe higher frequency of panhypopituitarism or developmental delay in patients with IHA. In control group, three had pars intermedia cysts, one hydrocephalus, and one hypothalamic hamartoma., Conclusion: FAST1.2 allows confident recognition of midline structural abnormalities, including the pituitary stalk and IHA, thereby making MRI acquisition faster and with no need for contrast administration. IHA could be associated with defects in neuronal migration, as occur in patients with EPP, with no clinical significance.
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- 2022
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30. Molecular, Histological and Histochemical Responses of Banana Cultivars Challenged with Fusarium oxysporum f. sp. cubense with Different Levels of Virulence.
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Rocha AJ, Soares JMDS, Nascimento FDS, Rocha ADS, Amorim VBO, Ramos APS, Ferreira CF, Haddad F, and Amorim EP
- Abstract
Fusarium wilt caused by Fusarium oxysporum f. sp. cubense (Foc) is the most limiting factor in the banana agribusiness worldwide. Therefore, studies regarding pathogen attack mechanisms, and especially host defense responses, in this pathosystem are of utmost importance for genetic breeding programs in the development of Foc-resistant banana cultivars. In this study, analysis at the molecular, histological and histochemical levels of the Musa spp. x Foc interaction was performed. Three Foc isolates representative of race 1 (R1), subtropical race 4 (ST4) and isolate 229A, which is a putative ST4, were inoculated in two Prata-type cultivars (Prata-Anã and BRS Platina) and one cultivar of the Cavendish type (Grand Naine). Of seven genes related to plant-pathogen interactions, five were overexpressed in 'BRS Platina' 12 h after inoculation (HAI) with Foc R1 and ST4 but had reduced or negative expression after inoculation with Foc 229A, according to RT-qPCR analyses. While hyphae, mycelia and spores of the Foc 229A isolate grow towards the central cylinder of the Grand Naine and Prata-Anã cultivars, culminating in the occlusion of the xylem vessels, the BRS Platina cultivar responds with increased presence of cellulose, phenolic compounds and calcium oxalate crystals, reducing colonization within 30 days after inoculation (DAI). In general, these data indicate that the cultivar BRS Platina has potential for use in banana-breeding programs focused on resistance to Foc tropical race 4 (TR4) and in aggregating information on the virulence relationships of the Foc pathogen and the defense responses of banana plants after infection.
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- 2022
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31. Forging Connections in Latin America to Advance AI in Radiology.
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Kitamura FC, do Nascimento FBP, Elizondo-Riojas G, Chaves H, Henríquez Leighton H, Salinas-Miranda E, Júlio T, da Rocha AJ, and Nomura CH
- Abstract
The 1° Encontro Latino-Americano de IA em Saúde (1st Latin American Meeting on AI in Health) was held during the 2022 Jornada Paulista de Radiologia, the annual radiology meeting in the state of São Paulo. The event was created to foster discussion among Latin American countries about the complexity, challenges, and opportunities in developing and using artificial intelligence (AI) in those countries. Technological improvements in AI have created high expectations in health care. AI is recognized increasingly as a game changer in clinical radiology. To counter the fear that AI would "take over" radiology, the program included activities to educate radiologists. The development of AI in Latin America is in its early days, and although there are some pioneer cases, many regions still lack world-class technological infrastructure and resources. Legislation, regulation, and public policies in data privacy and protection, digital health, and AI are recent advances in many countries. The meeting program was developed with a broad scope, with expertise from different countries, backgrounds, and specialties, with the objective of encompassing all levels of complexity (from basic concepts to advanced techniques), perspectives (clinical, technical, ethical, and business), and specialties (both informatics and data science experts and the usual radiology clinical groups). It was an opportunity to connect with peers from other countries and share lessons learned about AI in health care in different countries and contexts. Keywords: Informatics, Use of AI in Education, Impact of AI on Education, Social Implications © RSNA, 2022., Competing Interests: Disclosures of conflicts of interest: F.C.K. Consultant for MD.ai and GE Healthcare; co-chair of the Machine Learning Education Subcommittee at the Society for Imaging Informatics in Medicine; member of Radiological Society of North America (RSNA) Machine Learning Steering Committee; former member of Radiology In Training trainee editorial board. F.B.P.d.N. No relevant relationships. G.E.R. Leadership or fiduciary role in the RSNA Committee on International Radiology Education, Educación Committee at Federación Mexicana de Radiología e Imagen, and Evaluación Committee at Consejo Mexicano de Radiología e Imagen. H.C. Consulting fees from Entelai. H.H.L. No relevant relationships. E.S.M. No relevant relationships. T.J. Informatics director of Sociedade Paulista de Radiologia. A.J.d.R. No relevant relationships. C.H.N. No relevant relationships., (© 2022 by the Radiological Society of North America, Inc.)
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- 2022
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32. Gene Expression, Histology and Histochemistry in the Interaction between Musa sp. and Pseudocercospora fijiensis .
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Soares JMDS, Rocha AJ, Nascimento FDS, Amorim VBO, Ramos APS, Ferreira CF, Haddad F, and Amorim EP
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Bananas are the main fruits responsible for feeding more than 500 million people in tropical and subtropical countries. Black Sigatoka, caused by the fungus Pseudocercospora fijiensis , is one of the most destructive disease for the crop. This fungus is mainly controlled with the use of fungicides; however, in addition to being harmful to human health, they are associated with a high cost. The development of resistant cultivars through crosses of susceptible commercial cultivars is one of the main focuses of banana breeding programs worldwide. Thus, the objective of the present study was to investigate the interaction between Musa sp. and P. fijiensis through the relative expression of candidate genes involved in the defence response to black Sigatoka in four contrasting genotypes (resistant: Calcutta 4 and Krasan Saichon; susceptible: Grand Naine and Akondro Mainty) using quantitative real-time PCR (RT-qPCR) in addition to histological and histochemical analyses to verify the defence mechanisms activated during the interaction. Differentially expressed genes (DEGs) related to the jasmonic acid and ethylene signalling pathway, GDSL-like lipases and pathogenesis-related proteins (PR-4), were identified. The number and distance between stomata were directly related to the resistance/susceptibility of each genotype. Histochemical tests showed the production of phenolic compounds and callosis as defence mechanisms activated by the resistant genotypes during the interaction process. Scanning electron microscopy (SEM) showed pathogenic structures on the leaf surface in addition to calcium oxalate crystals. The resistant genotype Krasan Saichon stood out in the analyses and has potential for use in breeding programs for resistance to black Sigatoka in banana and plantains.
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- 2022
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33. Adding T2-Weighted Images to FAST1 Protocol to Evaluate the Anatomy of the Hypothalamic-Pituitary Region.
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Meira AS, Lyra A, Kochi C, Guimarães DF, Nunes ACB, Peixoto GV, Zamot SG, E Silva TS, da Rocha AJ, and Longui CA
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- Humans, Magnetic Resonance Imaging, Pituitary Gland diagnostic imaging, Pituitary Hormones, Retrospective Studies, Dwarfism, Pituitary, Human Growth Hormone, Hypopituitarism diagnostic imaging, Pituitary Diseases diagnostic imaging
- Abstract
Introduction: Ectopic posterior pituitary (EPP) is a malformation of the hypothalamic-pituitary region presented as a spectrum from isolated growth hormone deficiency (GHD) to multiple pituitary hormone deficiencies (MPHDs). Our goal was to establish whether the FAST1.2 protocol, which combines the FAST1 protocol with 3D-T2 DRIVE images, could identify the pituitary stalk (PS) and the regional anatomy more accurately., Methods: A retrospective study of 36 individuals with EPP and hypopituitarism and a control group of 78 individuals with eutopic posterior pituitary was conducted. All individuals were submitted to FAST1.2. The position and size of the pituitary lobes were described, and the presence/absence of the PS was confirmed., Results: FAST1 identified the PS in 19% of individuals with EPP, while FAST1.2 identified the PS in 67% (p < 0.001). In the FAST1.2 protocol, the PS was visible in all control individuals. All EPP patients with isolated GHD had visible PS in FAST1.2, while only 58.6% of MPHD cases had visible PS. The size of the anterior lobe and the anteroposterior length of the posterior pituitary were smaller in the EPP group versus controls (p < 0.001). We noticed a reduced anterior pituitary lobe in both diameters in MPHD patients (p < 0.05). Six patients acquired new pituitary hormone deficiencies not recognized at the time of MRI; in this group, only 1 patient had a PS not visible in FAST1.2., Discussion/conclusion: The FAST1.2 protocol could prevent the misdiagnosis of idiopathic GHD in patients with short stature and could also be important in the progression to MPHD. The PS could be considered a predictor of hypopituitarism, but its use as an isolated indicator for the progression to MPHD is not recommended. Our results reinforce the use of the size of the anterior lobe as a predictor of hypopituitarism and a possible predictor of the degree of pituitary insufficiency. The FAST1.2 protocol could be used as an alternative to gadolinium administration, as a cheaper and faster method, while eliminating the potential risks associated with the administration of contrast media., (© 2022 S. Karger AG, Basel.)
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- 2022
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34. Genetic Improvement for Resistance to Black Sigatoka in Bananas: A Systematic Review.
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Soares JMS, Rocha AJ, Nascimento FS, Santos AS, Miller RNG, Ferreira CF, Haddad F, Amorim VBO, and Amorim EP
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Bananas are an important staple food crop in tropical and subtropical regions in Asia, sub-Saharan Africa, and Central and South America. The plant is affected by numerous diseases, with the fungal leaf disease black Sigatoka, caused by Mycosphaerella fijiensis Morelet [anamorph: Pseudocercospora fijiensis (Morelet) Deighton], considered one of the most economically important phytosanitary problem. Although the development of resistant cultivars is recognized as most effective method for long term control of the disease, the majority of today's cultivars are susceptible. In order to gain insights into this pathosystem, this first systematic literature review on the topic is presented. Utilizing six databases (PubMed Central, Web of Science, Google Academic, Springer, CAPES and Scopus Journals) searches were performed using pre-established inclusion and exclusion criteria. From a total of 3,070 published studies examined, 24 were relevant with regard to the Musa-P. fijiensis pathosystem. Relevant papers highlighted that resistant and susceptible cultivars clearly respond differently to infection by this pathogen. M. acuminata wild diploids such as Calcutta 4 and other diploid cultivars can harbor sources of resistance genes, serving as parentals for the generation of improved diploids and subsequent gene introgression in new cultivars. From the sequenced reference genome of Musa acuminata , although the function of many genes in the genome still require validation, on the basis of transcriptome, proteome and biochemical data, numerous candidate genes and molecules have been identified for further evaluation through genetic transformation and gene editing approaches. Genes identified in the resistance response have included those associated with jasmonic acid and ethylene signaling, transcription factors, phenylpropanoid pathways, antioxidants and pathogenesis-related proteins. Papers in this study also revealed gene-derived markers in Musa applicable for downstream application in marker assisted selection. The information gathered in this review furthers understanding of the immune response in Musa to the pathogen P. fijiensis and is relevant for genetic improvement programs for bananas and plantains for control of black Sigatoka., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Soares, Rocha, Nascimento, Santos, Miller, Ferreira, Haddad, Amorim and Amorim.)
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- 2021
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35. Primary Angiitis of the CNS with Unremarkable Vessel Wall MR Imaging: How the "T1 Shinethrough" Effect on SWI Adds to the Detection of Gadolinium Enhancement of Small Intraparenchymal Brain Vessels.
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Fonseca APA, do Carmo RL, Pacheco FT, Nunes RH, and da Rocha AJ
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- Brain diagnostic imaging, Contrast Media, Humans, Magnetic Resonance Imaging, Gadolinium, Vasculitis
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- 2021
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36. Improvements in the Resistance of the Banana Species to Fusarium Wilt: A Systematic Review of Methods and Perspectives.
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Rocha AJ, Soares JMDS, Nascimento FDS, Santos AS, Amorim VBO, Ferreira CF, Haddad F, Santos-Serejo JAD, and Amorim EP
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The fungus Fusarium oxysporum f. sp. cubense (FOC), tropical race 4 (TR4), causes Fusarium wilt of banana, a pandemic that has threatened the cultivation and export trade of this fruit. This article presents the first systematic review of studies conducted in the last 10 years on the resistance of Musa spp. to Fusarium wilt. We evaluated articles deposited in different academic databases, using a standardized search string and predefined inclusion and exclusion criteria. We note that the information on the sequencing of the Musa sp. genome is certainly a source for obtaining resistant cultivars, mainly by evaluating the banana transcriptome data after infection with FOC. We also showed that there are sources of resistance to FOC race 1 (R1) and FOC TR4 in banana germplasms and that these data are the basis for obtaining resistant cultivars, although the published data are still scarce. In contrast, the transgenics approach has been adopted frequently. We propose harmonizing methods and protocols to facilitate the comparison of information obtained in different research centers and efforts based on global cooperation to cope with the disease. Thus, we offer here a contribution that may facilitate and direct research towards the production of banana resistant to FOC.
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- 2021
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37. Neuroradiologic Phenotyping of Galactosemia: From the Neonatal Form to the Chronic Stage.
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Rossi-Espagnet MC, Sudhakar S, Fontana E, Longo D, Davison J, Petengill AL, Bevivino E, Pacheco FT, da Rocha AJ, Hanagandi P, Soldatelli M, Mankad K, and do Amaral LLF
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- Adolescent, Child, Child, Preschool, Disease Progression, Female, Humans, Infant, Infant, Newborn, Male, Brain diagnostic imaging, Brain pathology, Galactosemias diagnostic imaging, Galactosemias pathology
- Abstract
Galactosemia is a rare genetic condition caused by mutation of enzymes involved in galactose and glucose metabolism. The varying clinical spectrum reflects the genetic complexity of this entity manifesting as acute neonatal toxicity syndrome, requiring prompt diagnosis and treatment, to more insidious clinical scenarios as observed in the subacute and chronic presentations. The current literature predominantly focuses on the long-standing sequelae of this disease. The purpose of this multicenter clinical report comprising 17 patients with galactosemia is to highlight the MR imaging patterns encompassing the whole spectrum of galactosemia, emphasizing the 3 main clinical subtypes: 1) acute neonatal presentation, with predominant white matter edema; 2) subacute clinical onset with a new finding called the "double cap sign"; and 3) a chronic phase of the disease with heterogeneous imaging findings. The knowledge of these different patterns together with MR spectroscopy and the clinical presentation may help in prioritizing galactosemia over other neonatal metabolic diseases and prevent possible complications., (© 2021 by American Journal of Neuroradiology.)
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- 2021
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38. Severe progressive brain involvement in a patient with TRMT10C mutation.
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Camelo CG, Silva AMS, Rocha AJ, Scaramuzzi V, Moreno CAM, Reed UC, and Zanoteli E
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- Female, Humans, Infant, Mutation, Brain diagnostic imaging, Brain metabolism, Methyltransferases genetics, Methyltransferases metabolism
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- 2021
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39. Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study.
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Inada BSY, Rezende TJR, Pereira FV, Garcia LÁL, da Rocha AJ, Neto PB, Barsottini OGP, França MC Jr, and Pedroso JL
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- Diffusion Tensor Imaging, Humans, Internal Capsule, Machado-Joseph Disease diagnostic imaging, Pyramidal Tracts diagnostic imaging, White Matter diagnostic imaging
- Abstract
Purpose: The aim of this study was to evaluate the integrity of the corticospinal tracts (CST) in patients with SCA3 and age- and gender-matched healthy control subjects using diffusion tensor imaging (DTI). We also looked at the clinical correlates of such diffusivity abnormalities., Methods: We assessed 2 cohorts from different Brazilian centers: cohort 1 (n = 29) scanned in a 1.5 T magnet and cohort 2 (n = 91) scanned in a 3.0 T magnet. We used Pearson's coefficients to assess the correlation of CST DTI parameters and ataxia severity (expressed by SARA scores)., Results: Two different results were obtained. Cohort 1 showed no significant between-group differences in DTI parameters. Cohort 2 showed significant between-group differences in the FA values in the bilateral precentral gyri (p < 0.001), bilateral superior corona radiata (p < 0.001), bilateral posterior limb of the internal capsule (p < 0.001), bilateral cerebral peduncle (p < 0.001), and bilateral basis pontis (p < 0.001). There was moderate correlation between CST diffusivity parameters and SARA scores in cohort 2 (Pearson correlation coefficient: 0.40-0.59)., Conclusion: DTI particularly at 3 T is able to uncover and quantify CST damage in SCA3. Moreover, CST microstructural damage may contribute with ataxia severity in the disease.
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- 2021
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40. Femoral fractures in the elderly in Brasil - incidence, lethality, and costs (2008-2018).
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Vasconcelos PAB, Rocha AJ, Fonseca RJS, Teixeira TRG, Mattos ESR, and Guedes A
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- Aged, Brazil epidemiology, Cross-Sectional Studies, Female, Hospitalization, Humans, Incidence, Male, Retrospective Studies, Femoral Fractures epidemiology
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Objectives: To describe the incidence by gender and region, lethality, and costs associated with the treatment of femoral fractures in the elderly (≥ 60 years) hospitalized in the Unified Health System (SUS) of Brasil between 2008 and 2018., Methods: This is a cross-sectional, descriptive, retrospective study of hospitalizations of elderly people due to femoral fractures by analyzing secondary data obtained from the SUS Hospital Information System (SIH/SUS) between 2008 and 2018; for calculation of epidemiological coefficients, we used information from demographic censuses (2000 and 2010) of the Brazilian Geography and Statistics Institute (IBGE)., Results: A total of 478,274 hospitalizations were recorded in the period; the incidence was 1.7 times higher in females (overall average of 274.91/100,000 for women and 161/100,000 for men). The Southeast region had the highest absolute number of hospitalizations and the South region presented the highest annual overall average incidence (224.02/100,000). The average annual cost for SUS for the treatment of femoral fractures in the elderly was R$ 99,718,574.30., Conclusions: In the evaluated period (2008-2018), femoral fractures in the elderly had a high incidence (478,274 hospitalizations; 224.02 cases/100,000 elderly), a predominance of females (1.7F/1.0M), a higher absolute number of hospitalizations in the Southeast region and a higher incidence in the South region; the lethality was high (an increase of 17.46%; overall mean coefficient of 4.99%/year); and the costs for the SUS were huge (an increase of 126.24%; average annual expenditure of R$ 99,718,574.30).
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- 2020
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41. First molecular evidence of Theileria cervi infection in white-tailed deer (Odocoileus virginianus) in Mexico.
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Pavón-Rocha AJ, Cárdenas-Flores A, Rábago-Castro JL, Barrón-Vargas CA, and Mosqueda J
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- Animals, Mexico epidemiology, Polymerase Chain Reaction veterinary, Ticks, Deer parasitology, Theileria genetics, Theileriasis epidemiology
- Abstract
Theileria cervi is a tick-borne protozoan that infects different deer species around the world. Clinical diseases due to Theileria cervi have been reported in white-tailed deer (Odocoileus virginianus) and mule deer (Odocoileus hemionus) in the USA, however, information about this parasite has not been documented in Mexico. Here, blood samples from three white-tailed deer (Odocoileus virginianus) from a region in northeastern Mexico were analyzed by blood smear, PCR, and DNA sequencing. The results confirmed the presence of T. cervi for the first time in white-tailed deer in Mexico., (Copyright © 2020 Elsevier B.V. All rights reserved.)
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- 2020
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42. Cerebellar gangliocytoma as a cause of fluctuating hearing loss.
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Rocha AJ, Márquez R, and García-Berrocal JR
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Cerebellar lesions could be a cause of fluctuating hearing loss, due to the increase of intracranial pressure by partially or complete blocking of the Foramen of Luschka. Patients with intracranial hypertension may present audio-vestibular symptoms. Fluctuating sensorineural hearing loss may be the manifestation of different inner ear disorders such as Meniere's disease (MD), immune-mediated inner ear disease (IMIED), otosyphilis, and labyrinthine fistula including semicircular canal dehiscence. A rare mechanism involved in the fluctuating hearing loss is the increase in cerebrospinal fluid (CSF) pressure, that may be caused by a cerebellar tumor. A 51-year-old female presented a 2-year history of left ear fluctuating hearing loss and tinnitus, with fluctuations among the day, and normal otoscopy. Several audiometries showed a left ear moderate sensorineural hearing loss in low frequencies (Figure 1). The patient underwent a cerebral magnetic resonance imaging (MRI) (Figure 2). She was treated with three courses of systemic steroids showing improvement of symptoms during the treatment. However, the symptoms always returned when corticotherapy was interrupted. The patient was given two intratympanic steroids cycles combined with hydrochlorothiazide/ amiloride hydrochloride. The cerebral MRI described a left cerebellar focal lesion diagnosed as a cerebellar gangliocytoma. After receiving the second intratympanic steroids, cycle combined with systemic ameride showed a significant improvement of audition. Between the several causes of fluctuating hearing loss, a cerebellar gangliocytoma is a very rare disease, which needs a high degree of suspicion and otorhinolaryngologists should be familiar with this entity since patients may present with audiological and vestibular symptoms., Competing Interests: None declared., (© 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.)
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- 2020
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43. Association between brain morphology and electrophysiological features in Congenital Zika Virus Syndrome: A cross-sectional, observational study.
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Sequerra EB, Rocha AJ, de Medeiros GOC, Neto MM, Maia CRS, Arrais NMR, Bezerra M, Jeronimo SMB, Barros AK, Sousa PS, Nogueira de Melo A, and Queiroz CM
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Background: Intrauterine infection with the Zika virus (ZIKV) has been connected to severe brain malformations, microcephaly, and abnormal electrophysiological activity., Methods: We describe the interictal electroencephalographic (EEG) recordings of 47 children born with ZIKV-derived microcephaly. EEGs were recorded in the first year of life and correlated with brain morphology. In 31 subjects, we tested the association between computed tomography (CT) findings and interictal epileptiform discharges (IED). In eighteen, CTs were used for correlating volumetric measurements of the brainstem, cerebellum, and prosencephalon with the rate of IED., Findings: Twenty-nine out of 47 (62%) subjects were diagnosed as having epilepsy. Those subjects presented epileptiform discharges, including unilateral interictal spikes (26/29, 90%), bilateral synchronous and asynchronous interictal spikes (21/29, 72%), and hypsarrhythmia (12/29, 41%). Interestingly, 58% of subjects with clinical epilepsy were born with rhombencephalon malformations, while none of the subjects without epilepsy showed macroscopic abnormalities in this region. The presence of rhombencephalon malformation was associated with epilepsy (odds ratio of 34; 95% CI: 2 - 654). Also, the presence of IED was associated with smaller brain volumes. Age-corrected total brain volume was inversely correlated with the rate of IED during sleep. Finally, 11 of 44 (25%) subjects presented sleep spindles. We observed an odds ratio of 0·25 (95% CI: 0·06 - 1·04) for having sleep spindles given the IED presence., Interpretation: The findings suggest that certain CT imaging features are associated with an increased likelihood of developing epilepsy, including higher rates of IED and impaired development of sleep spindles, in the first year of life of CZVS subjects., Funding: This work was supported by the Brazilian Federal Government through a postdoctoral fellowship for EBS (Talented Youth, Science without Borders), an undergraduate scholarship for AJR (Institutional Program of Science Initiation Scholarships, Federal University of Rio Grande do Norte, Brazil), by International Centre for Genetic Engineering and Biotechnology (CRP/BRA18-05_EC) and by CAPES (Grant number 440893/2016-0), and CNPq (Grant number 88881.130729/2016-01)., Competing Interests: We declare no competing interests associated with this work., (© 2020 The Authors.)
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- 2020
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44. Practical recommendations for the safe use of gadolinium in magnetic resonance imaging: a Delphi expert panel study.
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Baroni RH, Bauab T Jr, Bittencourt LK, D'Ippolito G, Goldman SM, Hohgraefe Neto G, Manzella A, Rocha AJ, Sonoda LA, and Takeda FS
- Abstract
Objective: To assess the practical aspects of the use of various gadolinium-based contrast agents (GBCAs) by radiologists., Materials and Methods: Ten experienced radiologists from different regions of Brazil participated in a Delphi panel querying their use of various GBCAs, including linear and macrocyclic classes (1.0 and 0.5 M), in terms of the choice of agent, volume and dosage of the agents, and associated safety concerns., Results: The response rate was 100% for all questions. GBCAs are safe in terms of acute adverse reactions, and nephrogenic systemic fibrosis is rare. The deposition of gadolinium in the brain and other tissues is a concern among the experts. Macrocyclic agents are preferable to linear agents; an injection volume below 0.1 mL/kg of a 1.0 M agent could result in good-quality images with additional long-term safety, but there is no published evidence to support this recommendation. The majority of experts preferred not to administer GBCAs to pregnant patients., Conclusion: When choosing a GBCA, it is important to consider the characteristics of the gadolinium deposition in patient tissues and minimize potential risks. Furthermore, medical education programs are needed to increase the awareness of the potential risks of gadolinium deposition and thus avoid instances of overexposure to the contrast agent.
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- 2020
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45. Case 278: Mutation in ROBO3 Gene-Horizontal Gaze Palsy and Progressive Scoliosis.
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Scortegagna FA, Pacheco FT, Nunes RH, Serpa A, Migliavacca MP, and da Rocha AJ
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- Adolescent, Consanguinity, Female, Humans, Magnetic Resonance Imaging, Ophthalmoplegia, Chronic Progressive External diagnostic imaging, Rare Diseases, Scoliosis diagnostic imaging, DNA Mutational Analysis, Ophthalmoplegia, Chronic Progressive External genetics, Receptors, Cell Surface genetics, Scoliosis genetics
- Abstract
HistoryA 13-year-old girl was born to consanguineous parents. She presented with mild intellectual impairment, convergent strabismus, horizontal gaze palsy, and bilateral abducens palsy. Vertical gaze was preserved, and no abnormalities suggesting facial paralysis were noted. In addition, she reported progressive back pain since she was 5 years old. Other symptoms were denied. No medications or related drugs had been administered thus far. The patient underwent brain MRI for further evaluation. Current and previous spine radiographs were also reviewed.
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- 2020
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46. Pediatric multiple sclerosis: from clinical basis to imaging spectrum and differential diagnosis.
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Padilha IG, Fonseca APA, Pettengill ALM, Fragoso DC, Pacheco FT, Nunes RH, Maia ACM Jr, and da Rocha AJ
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- Age of Onset, Child, Diagnosis, Differential, Humans, Multiple Sclerosis diagnostic imaging
- Abstract
Pediatric multiple sclerosis (MS) deserves special attention because of its impact on cognitive function and development. Although knowledge regarding pediatric MS has rapidly increased, understanding the peculiarities of this population remains crucial for disease management. There is limited expertise about the efficacy and safety of current disease-modifying agents. Although pathophysiology is not entirely understood, some risk factors and immunological features have been described and are discussed herein. While the revised International Pediatric MS Study Group diagnostic criteria have improved the accuracy of diagnosis, the recently revised McDonald criteria also offer some new insights into the pediatric population. It is fundamental that radiologists have strong knowledge about the vast spectrum of demyelinating disorders that can occur in childhood to ensure appropriate diagnosis and provide early treatment.
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- 2020
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47. POLR3A -Related Disorder Presenting with Late-Onset Dystonia and Spastic Paraplegia.
- Author
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de Assis Pereira Matos PCA, Gama MTD, Bezerra MLE, da Rocha AJ, Barsottini OGP, and Pedroso JL
- Abstract
Competing Interests: The authors report no sources of funding and no conflicts of interest.
- Published
- 2020
- Full Text
- View/download PDF
48. Cerebral venous thrombosis in a 6-year-old boy with sickle cell trait.
- Author
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Vitturi BK, da Rocha AJ, and Rosemberg S
- Subjects
- Child, Humans, Male, Sickle Cell Trait complications, Sinus Thrombosis, Intracranial etiology
- Published
- 2020
- Full Text
- View/download PDF
49. [High seroprevalence of Neospora caninum in dogs with clinical suspicion of neosporosis in Montevideo, Uruguay].
- Author
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Satragno D, Pavón-Rocha AJ, Rábago-Castro JL, and la Cruz-Hernández NI
- Subjects
- Animals, Antibodies, Protozoan blood, Coccidiosis blood, Coccidiosis epidemiology, Dog Diseases blood, Dogs, Female, Male, Retrospective Studies, Seroepidemiologic Studies, Uruguay epidemiology, Coccidiosis veterinary, Dog Diseases epidemiology, Dog Diseases parasitology, Neospora immunology
- Published
- 2020
- Full Text
- View/download PDF
50. Case 278.
- Author
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Scortegagna FA, Pacheco FT, Nunes RH, Serpa A, Migliavacca MP, and da Rocha AJ
- Abstract
HistoryA 13-year-old girl was born to consanguineous parents. She presented with mild intellectual impairment, convergent strabismus, horizontal gaze palsy, and bilateral abducens palsy. Vertical gaze was preserved, and no abnormalities suggesting facial paralysis were noted. In addition, she reported progressive back pain since she was 5 years old. Other symptoms were denied. No medications or related drugs had been administered thus far.
- Published
- 2020
- Full Text
- View/download PDF
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