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2. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

4. How Encephalopathy Impacts Language Ability: A Scoping Review of the Linguistic Abilities of Adults with Developmental and Epileptic Encephalopathy.

6. Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes

15. Branched-chain amino acids as adjunctive-alternative treatment in patients with autism: a pilot study.

16. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

17. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

19. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

20. Clinical, Neuroimaging, and Genetic Markers in Cerebral Amyloid Angiopathy-Related Inflammation: A Systematic Review and Meta-Analysis

24. Care in Europe after presenting to the emergency department with a seizure; position paper and insights from the European Audit of Seizure Management in Hospitals

28. Prevalence of Clinical and Neuroimaging Markers in Cerebral Amyloid Angiopathy: A Systematic Review and Meta-Analysis

31. Cerebral folate deficiency in two siblings caused by biallelic variants including a novel mutation ofFOLR1gene: Intrafamilial heterogeneity following early treatment and the role of ketogenic diet

32. Primary Sjögren's Syndrome Presenting with Rapidly Progressive Dementia: A Case Report

38. Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients

39. West Nile neuroinvasive disease. Report of four cases in Northern Greece, 2018

41. AΥΤΟΑΝΟΣΗ ΠΑΡΑΝΕΟΠΛΑΣΜΑΤΙΚΗ ΑΝΤΙ-GABAb ΛΙΜΒΙΚΗ ΕΓΚΕΦΑΛΙΤΙΔΑ ΜΕ ΣΥΝΥΠΑΡΞΗ ΟΓΚΟΝΕΥΡΩΝΙΚΩΝ ΑΝΤΙΣΩΜΑΤΩΝ

47. Additional file 1: FigureS1. of Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia

48. Spine pathology in a girl with upper limb pain: A co-incidence or a causal relationship?

49. Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia

50. ΠΡΩΤΟΠΑΘΕΣ ΛΕΜΦΩΜΑ ΤΟΥ ΚΕΝΤΡΙΚΟΥ ΝΕΥΡΙΚΟΥ ΣΥΣΤΗΜΑΤΟΣ ΜΕ ΑΠΕΙΚΟΝΙΣΤΙΚΑ ΕΥΡΗΜΑΤΑ ΣΥΜΒΑΤΑ ΜΕ ΔΙΑΣΠΑΡΤΗ ΕΓΚΕΦΑΛΟΜΥΕΛΙΤΙΔΑ

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