Search

Your search keyword '"Rita Guerreiro"' showing total 274 results

Search Constraints

Start Over You searched for: Author "Rita Guerreiro" Remove constraint Author: "Rita Guerreiro"
274 results on '"Rita Guerreiro"'

Search Results

1. O Custo da Meningite Meningocócica em Portugal

2. Genome-wide association of polygenic risk extremes for Alzheimer's disease in the UK Biobank

3. Challenge accepted: uncovering the role of rare genetic variants in Alzheimer’s disease

4. Reconsidering the role of blood-brain barrier in Alzheimer’s disease: From delivery to target

6. A comprehensive analysis of copy number variation in a Turkish dementia cohort

7. PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

8. Exome Sequencing of a Portuguese Cohort of Frontotemporal Dementia Patients: Looking Into the ALS-FTD Continuum

9. A deletion of IDUA exon 10 in a family of Golden Retriever dogs with an attenuated form of mucopolysaccharidosis type I

10. Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

11. An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids

12. Heritability and genetic variance of dementia with Lewy bodies

14. Disease-related cortical thinning in presymptomatic granulin mutation carriers

15. Differential early subcortical involvement in genetic FTD within the GENFI cohort

16. The association of circulating amylin with β‐amyloid in familial Alzheimer's disease

17. Polygenic risk scores for Alzheimer's disease are related to dementia risk in APOE ɛ4 negatives

18. Genetic architecture of common non-Alzheimer’s disease dementias

19. A Era da Multirresistência: Incidência em Dez Anos Numa Unidade de Cuidados Intensivos Neonatais

20. Molecular Characterization of Portuguese Patients with Hereditary Cerebellar Ataxia

21. Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience

22. TBC1D24 Mutations in a Sibship with Multifocal Polymyoclonus

23. Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.

24. Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease.

25. Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience

26. NOTCH3 variants and risk of ischemic stroke.

27. Identification of Stk25 as a genetic modifier of Tau phosphorylation in Dab1-mutant mice.

28. As quimiocinas e os seus receptores: características e funções fisiológicas.

29. Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease.

30. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.

31. Introductory Note

33. The Role of International Organizations in the Development of International Environmental Law: Adjusting the Lenses of Analysis.

34. Research Handbook on the Theory and Practice of International Lawmaking.

35. A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia

36. New insights into the genetic etiology of Alzheimer's disease and related dementias

37. Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease

38. Rare variants in TP73 in a frontotemporal dementia cohort link this gene with primary progressive aphasia phenotypes

39. Genetic analysis ofVCPvariants in a Turkish dementia cohort

40. Genetic characterization of a Turkish dementia cohort: a focus on leukodystrophy genes

41. Vasculitic peripheral neuropathy in deficiency of adenosine deaminase 2

42. Identification of a sex-specific genetic signature in dementia with Lewy bodies: a meta-analysis of genome-wide association studies

43. TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features

44. Congenital ataxia due to novel variant in <scp> ATP8A2 </scp>

45. MED27, SLC6A7, and MPPE1 variants in a complex neurodevelopmental disorder with severe dystonia

46. Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype-phenotype correlation

47. Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes

49. A Non-APOE Polygenic Risk Score for Alzheimer’s Disease Is Associated With Cerebrospinal Fluid Neurofilament Light in a Representative Sample of Cognitively Unimpaired 70-Year Olds

50. Psychiatric Manifestations of ATP13A2 Mutations

Catalog

Books, media, physical & digital resources