359 results on '"Arrigoni, Filippo"'
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2. Magnetic resonance imaging of intracranial anomalies in pregnancies complicated by twin anemia-polycythemia sequence
3. Spontaneous regression of an epidermoid cyst in a pediatric patient—Case report and review of the literature
4. Alterations in neural activation in the ventral frontoparietal network during complex magnocellular stimuli in developmental dyslexia associated with READ1 deletion
5. Cutting-edge applications of fetal MR neuro-imaging in clinical routine: a pictorial essay
6. Onset of Chiari type 1 malformation: insights from a small series of intrauterine MR imaging cases
7. Congenital Cytomegalovirus Infection With Isolated “Minor” Lesions at Fetal Magnetic Resonance Imaging: Long-Term Neurological Outcome
8. Therapeutic Use of Interferon Gamma in Friedreich Ataxia
9. Congenital isolated unilateral third nerve palsy in children: the diagnostic contribution of high-resolution MR imaging
10. Automatic Tissue Segmentation with Deep Learning in Patients with Congenital or Acquired Distortion of Brain Anatomy
11. Get Your Molar Tooth Right: Joubert Syndrome Misdiagnosis Unmasked by Whole-Exome Sequencing
12. DBB - A Distorted Brain Benchmark for Automatic Tissue Segmentation in Paediatric Patients
13. A framework for optimizing the acquisition protocol multishell diffusion‐weighted imaging for multimodel assessment.
14. A multi-metric registration strategy for the alignment of longitudinal brain images in pediatric oncology
15. Tubulin genes and malformations of cortical development
16. Automatic Tissue Segmentation with Deep Learning in Patients with Congenital or Acquired Distortion of Brain Anatomy
17. The spectrum of brainstem malformations associated to mutations of the tubulin genes family: MRI and DTI analysis
18. A framework for the automatic detection and characterization of brain malformations: Validation on the corpus callosum
19. Detection of Corpus Callosum Malformations in Pediatric Population Using the Discriminative Direction in Multiple Kernel Learning
20. Cognitive rehabilitation in a child with Joubert Syndrome: Developmental trends and adaptive changes in a single case report
21. Brain Alteration Patterns in Children with Duchenne Muscular Dystrophy: A Machine Learning Approach to Magnetic Resonance Imaging
22. Conventional MRI
23. Tubulinopathies
24. Mutations in α- and β-tubulin encoding genes: Implications in brain malformations
25. Congenital isolated unilateral third nerve palsy in children: the diagnostic contribution of high-resolution MR imaging
26. Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation
27. Progressive Spinal Cord Degeneration in Friedreich's Ataxia: Results from ENIGMA‐Ataxia
28. EEG at onset and MRI predict long-term clinical outcome in Aicardi syndrome
29. Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement
30. Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents
31. Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype
32. Superior Cerebellar Atrophy: An Imaging Clue to Diagnose ITPR1-Related Disorders
33. Biallelic loss of EMC10 leads to mild to severe intellectual disability
34. Effects of age and gender on neural correlates of emotion imagery
35. Quantitative MRI Harmonization to Maximize Clinical Impact: The RIN–Neuroimaging Network
36. Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement
37. Functional MRI Studies in Friedreich's Ataxia: A Systematic Review
38. Quantitative MRI Harmonization to Maximize Clinical Impact: The RIN???Neuroimaging Network
39. A diffusion tensor magnetic resonance imaging study of paediatric patients with severe non‐traumatic brain injury
40. Spinal cord damage in Friedreich’s ataxia: Results from the ENIGMA-Ataxia
41. Functional MRI Studies in Friedreich's Ataxia: A Systematic Review
42. Long‐term follow‐up in a cohort of children with isolated corpus callosum agenesis at fetal MRI
43. Get Your Molar Tooth Right: Joubert Syndrome Misdiagnosis Unmasked by Whole-Exome Sequencing
44. Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis
45. Investigation of the electrophysiological correlates of negative BOLD response during intermittent photic stimulation: An EEG-fMRI study
46. Progressive Spinal Cord Degeneration in Friedreich's Ataxia: Results from ENIGMA‐Ataxia.
47. Get Your Molar Tooth Right: Joubert Syndrome Misdiagnosis Unmasked by Whole-Exome Sequencing.
48. SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum
49. Brain Structure and Degeneration Staging in Friedreich Ataxia: Magnetic Resonance Imaging Volumetrics from the ENIGMA‐Ataxia Working Group
50. Investigation of negative BOLD responses in human brain through NIRS technique. A visual stimulation study
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