339 results on '"Fluss, Joel"'
Search Results
2. Reply to letter that comments on “Trigeminal nerve chronic motor denervation caused by cerebellar peduncle pilocytic astrocytoma”
3. Decompressive hemicraniectomy in pediatric malignant arterial ischemic stroke: a case-based review
4. Long-term developmental condition following neonatal arterial ischemic stroke: A systematic review
5. Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathy
6. Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders
7. Structural brain abnormalities in epilepsy with myoclonic atonic seizures
8. Molecular and Phenotypic Characterization of the RORB-Related Disorder
9. CAMTA1‐related disorder: Phenotypic and molecular characterization of 26 new individuals and literature review
10. Recognition, identification, and diagnosis announcement of neonatal arterial ischemic stroke: A combined exploratory quantitative and qualitative study on parents’ lived experiences
11. Cognitive and academic profiles in children with cerebral palsy: A narrative review
12. From congenial paralysis to post-early brain injury developmental condition: Where does cerebral palsy actually stand?
13. CAMTA1‐related disorder: Phenotypic and molecular characterization of 26 new individuals and literature review.
14. Impact of stroke volume on motor outcome in neonatal arterial ischemic stroke
15. Trigeminal nerve chronic motor denervation caused by cerebellar peduncle pilocytic astrocytoma
16. Health related quality of life and manual ability 5 years after neonatal ischemic stroke
17. Perinatal stroke syndromes: Similarities and diversities in aetiology, outcome and management
18. Modalities of reading acquisition in three siblings with infantile-onset saccade initiation delay (Cogan congenital ocular motor apraxia): A longitudinal study
19. Molecular and Phenotypic Characterization of the RORB-Related Disorder.
20. Successful heart transplant in a child with congenital core myopathy and delayed‐onset restrictive cardiomyopathy due to recessive mutations in the titin (TTN) gene
21. Fatal cervical myelopathy in a child with glutaric aciduria type 1.
22. Risk Factors for Postprocedural Arterial Ischemic Stroke in Children With Cardiac Disease
23. Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother
24. MRI of the first event in pediatric acquired demyelinating syndromes with antibodies to myelin oligodendrocyte glycoprotein
25. Développement à long terme après accident vasculaire cérébral ischémique artériel néonatal : quelles informations donner aux parents en néonatalogie ?
26. Multimodal Outcome at 7 Years of Age after Neonatal Arterial Ischemic Stroke
27. Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies
28. Gait stability in ambulant children with cerebral palsy during dual tasks
29. SERPINI1 pathogenic variants: An emerging cause of childhood‐onset progressive myoclonic epilepsy
30. SCN2A developmental and epileptic encephalopathy in an infant with bilateral polymicrogyria and opercular dysplasia
31. Transient Cerebral Arteriopathy, Postvaricella Arteriopathy, and Focal Cerebral Arteriopathy or the Unique Susceptibility of the M1 Segment in Children With Stroke
32. Cortical networks for vision and language in dyslexic and normal children of variable socio-economic status
33. Childhood-Onset Movement Disorders Can Mask a Primary Immunodeficiency: 6 Cases of Classical Ataxia-Telangiectasia and Variant Forms
34. Cohort profile: the Swiss Cerebral Palsy Registry (Swiss-CP-Reg) cohort study
35. High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families
36. SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum
37. Severe and Progressive Fetal Ventriculomegaly Leading to the Diagnosis of Periventricular Nodular Heterotopias with Good Outcome
38. Wallenberg Syndrome: An Exceptional Cause of Acute Vertigo in Children
39. SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum.
40. Hippocampal sclerosis and chronic epilepsy following posterior reversible encephalopathy syndrome
41. Planum temporale asymmetry in developmental dyslexia: Revisiting an old question
42. Partial Rhombencephalosynapsis and Chiari Type II Malformation in a Child: a True Association Supported by DTI Tractography
43. MRI with fibre tracking in Cogan congenital oculomotor apraxia
44. Positive Outcome following Early Diagnosis and Treatment of Pyridoxal-5′-Phosphate Oxidase Deficiency: A Case Report
45. Cerebral sinovenous thrombosis and idiopathic nephrotic syndrome in childhood: report of four new cases and review of the literature
46. ABCB1 polymorphisms and neuropsychiatric adverse events in oseltamivir-treated children during influenza H1N1/09 pandemia
47. Benzodiazepines in the acute management of seizures with autonomic manifestations: Anticipate complications!
48. Acute ischemic stroke in children versus young adults
49. Cerebral sinus venous thrombosis in Swiss children
50. Health related quality of life and manual ability 5 years after neonatal ischemic stroke
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