187 results on '"Arts, W."'
Search Results
2. Profile of pediatric Crohn's disease in Belgium
3. Stepping away from purified solvents in reductive catalytic fractionation: a step forward towards a disruptive wood biorefinery process.
4. The Future Biorefinery: The Impact of Upscaling the Reductive Catalytic Fractionation of Lignocellulose Biomass on the Quality of the Lignin Oil, Carbohydrate Products, and Pulp.
5. Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders
6. Clinical Course of Untreated Tonic-Clonic Seizures in Childhood: Prospective, Hospital Based Study
7. De kinderarts en diagnostiek van ontwikkelingsachterstand
8. LONG-TERM OUTCOME OF BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES: DUTCH STUDY OF EPILEPSY IN CHILDHOOD: 066
9. Quality of life in children with primary headache in a general hospital
10. Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhood
11. Early marrow transplantation in a pre-symptomatic neonate with late infantile metachromatic leukodystrophy does not halt disease progression
12. Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly
13. Histology of hereditary neuralgic amyotrophy
14. Interrater agreement of the diagnosis and classification of a first seizure in childhood. The Dutch Study of Epilepsy in Childhood
15. Neuroimaging in lissencephaly type I
16. Immunoglobulins in children with epilepsy: the Dutch Study of Epilepsy in Childhood
17. Nonsymptomatic Generalized Epilepsy in Children Younger than Six Years: Excellent Prognosis, but Classification Should Be Reconsidered after Follow-up: The Dutch Study of Epilepsy in Childhood
18. Enzyme therapy for Pompe disease with recombinant human α-glucosidase from rabbit milk
19. The Diagnostic Yield of a Second EEG After Partial Sleep Deprivation: A Prospective Study in Children with Newly Diagnosed Seizures
20. Seizure Severity in Children with Epilepsy: A Parent-Completed Scale Compared with Clinical Data
21. Restrictions in Childhood Epilepsy
22. Further investigations on benign myopathy with autosomal dominant inheritance
23. Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells
24. Boekbesprekingen - Reviews
25. Reviews
26. Familial myopathy with tubular aggregates
27. P-092: The course of anaemia in children with Crohn’s disease included in a prospective registry
28. The analysis of acquired dysarthria in childhood.
29. A case of myoglycogen storage disease with reduced acid α-glucosidase activity in the fibroblasts but not in the muscle
30. P550 Diagnosing and treating pediatric Crohn's disease patients: is there a difference between adult and pediatric gastroenterologists’ practices? Results of the BELCRO cohort
31. Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.
32. Safety and cost of infliximab for the treatment of belgian pediatric patients with Crohn's disease.
33. Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy.
34. P320 Factors determining therapeutic strategy at diagnosis and evolution of disease severity in a cohort of Belgian pediatric Crohn's disease patients (BELCRO)
35. P246 Safety and cost of infliximab for the treatment of Belgian pediatric patients with Crohn's disease
36. The accuracy of the diagnosis of paroxysmal events in children.
37. Clinical and genetic heterogeneity in benign hereditary chorea.
38. TO EACH HIS DUE: IDEAS OF SOCIAL JUSTICE AND DUTCH INCOME (RE)DISTRIBUTION POLICY.
39. Cerebellar and Brainstem Hypoplasia in a Child with a Partial Monosomy for the Short Arm of Chromosome 5 and Partial Trisomy for the Short Arm of Chromosome 10.
40. EEG and Evoked Potentials in a Series of 21 Patients with Lissencephaly Type I.
41. Late-Onset Globoid Cell Leucodystrophy (Krabbe's Disease).
42. Neuroimaging in lissencephaly type I.
43. Leukoencephalopathy with swelling and a discrepantly mild clinical course in eight children.
44. X-linked ataxia, weakness, deafness, and loss of vision in early childhood with a fatal course.
45. Segmental neurofibromatosis.
46. Significance of centro-temporal spikes on the EEG.
47. Disability due to restrictions in childhood epilepsy.
48. Diagnostic features and clinical signs of 21 patients with lissencephaly type 1.
49. Diagnostic Features And Clinical Signs Of 21 Patients With Lissencephaly Type I.
50. Familial myopathy with tubular aggregates.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.