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1. Outcome measures in Angelman syndrome

2. Autism Symptoms in Children and Young Adults With Fragile X Syndrome, Angelman Syndrome, Tuberous Sclerosis Complex, and Neurofibromatosis Type 1: A Cross-Syndrome Comparison

3. Predicting respiratory failure and outcome in pediatric Guillain-Barré syndrome

4. Meaningful outcomes for children and their caregivers attending a paediatric brain centre

5. Human RAD50 deficiency

6. Counselling in tuberous sclerosis complex: A survey on content and satisfaction in the Netherlands

7. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

8. A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statement

9. An overview of health issues and development in a large clinical cohort of children with Angelman syndrome

10. Everolimus for the treatment of refractory seizures associated with tuberous sclerosis complex (TSC): current perspectives

11. Everolimus for the treatment of refractory seizures associated with tuberous sclerosis complex (TSC): current perspectives

12. A randomized controlled trial with everolimus for IQ and autism in tuberous sclerosis complex

13. Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis

14. Biallelic DAB1 Variants Are Associated With Mild Lissencephaly and Cerebellar Hypoplasia

15. Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome

16. Examination of the genetic factors underlying the cognitive variability associated with neurofibromatosis type 1

17. Tuberous sclerosis complex

18. Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1

19. Motor nerve excitability after childhood Guillain-Barré syndrome

20. Diagnosis of Guillain–Barré syndrome in children and validation of the Brighton criteria

22. Radiation Exposure From Pediatric CT Scans and Subsequent Cancer Risk in the Netherlands

25. Response to Wollschlager, Blettner, and Pokora

28. Leerboek neurologie

29. Mycoplasma pneumoniae triggering the Guillain-Barré syndrome: A case-control study

30. Genotype and brain pathology phenotype in children with tuberous sclerosis complex

31. Sirolimus for epilepsy in children with tuberous sclerosis complex: A randomized controlled trial

32. Sodium Channel SCN3A (Na(V)1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development

33. Severe childhood Guillain-Barré syndrome associated with Mycoplasma pneumoniae infection: a case series

34. Incidental Findings on Brain Imaging in the General Pediatric Population

36. Motor problems in children with neurofibromatosis type 1

37. Author response: Sirolimus for epilepsy in children with tuberous sclerosis complex: A randomized controlled trial

38. Cortical dysplasia and autistic trait severity in children with Tuberous Sclerosis Complex: a clinical epidemiological study

39. Long-term outcome of Guillain-Barré syndrome in children

40. Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trial

41. Behandelingen voor genetische neurocognitieve aandoeningen

42. Novel no-stop FLNA mutation causes multi-organ involvement in males

43. Motor nerve excitability after childhood Guillain-Barré syndrome

44. Mycoplasma pneumoniae triggering the Guillain-Barré syndrome: A case-control study

45. RTTN Mutations Link Primary Cilia Function to Organization of the Human Cerebral Cortex

46. Asymmetric polymicrogyria and periventricular nodular heterotopia due to mutation inARX

47. Long-term follow-up of type 1 lissencephaly: survival is related to neuroimaging abnormalities

48. Combined cardiological and neurological abnormalities due to filamin A gene mutation

49. Periventricular nodular heterotopia and distal limb deficiency: A recurrent association

50. Cortical brain malformations - Effect of clinical, neuroradiological, and modern genetic classification

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