467 results on '"Heymans, H. S."'
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2. Small Intestinal Biopsy
3. Peroxisomal Disorders
4. Sociaal-maatschappelijke gevolgen en kwaliteit van leven in Nederland bij kinderen en jongvolwassenen opgegroeid met een chronische aandoening
5. Omvang en gevolgen van chronische aandoeningen bij kinderen
6. Alfa-1-antitrypsinedeficiëntie: klinische implicatie van een vouwdefect
7. De gezondheidsbeleving van jongvolwassen patiënten met een terminale nierinsufficiëntie sinds de kinderleeftijd is slechts gedeeltelijk gestoord
8. Subnormal response of plasma glucose concentration to glucagon despite adequate glycogenolysis: the importance of kinetic measurements
9. Ontwikkeling van allergische aandoeningen bij kinderen met koemelkallergie op de zuigelingenleeftijd
10. No detectable beneficial systemic immunomodulatory effects of a specific synbiotic mixture in infants with atopic dermatitis
11. Synbiotics prevent asthma-like symptoms in infants with atopic dermatitis
12. Effect of a new synbiotic mixture on atopic dermatitis in infants: a randomized-controlled trial
13. Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature
14. Kindergeneeskunde
15. Onderzoek bij kinderen en neonaten
16. Physical adaptation of children to life at high altitude
17. Tyrosinaemia type I: considerations of treatment strategy and experiences with risk assessment, diet and transplantation
18. Œsophagite par reflux: biopsie oui ou non?
19. A proposition for the diagnosis and treatment of gastro-oesophageal reflux disease in children: A report from a working group on gastro-oesophageal reflux disease
20. Clinical recognition of patients affected by a peroxisomal disorder: A retrospective study in 40 patients
21. Intestinal permeability in relation to birth weight and gestational and postnatal age
22. Gastrointestinal involvement in Langerhans' cell histiocytosis (Histiocytosis X): A clinical report of three cases
23. The inborn errors of peroxisomal β-oxidation: A review
24. Impaired cognition and schooling in adults with end stage renal disease since childhood
25. The effect of brief neonatal exposure to cows' milk on atopic symptoms up to age 5
26. De novo malignancy after paediatric renal replacement therapy
27. Development of allergic disorders in children with cowʼs milk protein allergy or intolerance in infancy
28. No association between glucocorticoid receptor polymorphisms and long-term respiratory outcome after very preterm birth.
29. The relation between gastro-oesophageal reflux, sleeping-position and sudden infant death and its impact on positional therapy
30. A patient with lethal cardiomyopathy and a carnitine — acylcarnitine translocase deficiency
31. Phenylketonuria: The In Vivo Hydroxylation Rate of Phenylalanine into Tyrosine Is Decreased
32. Severity scoring of atopic dermatitis: a comparison of three scoring systems
33. Onderzoek in de kindergeneeskunde, een bewogen beweging
34. Deficiencies in Ether Glycerolipids and Their Biosynthesis in Inherited Peroxisomal Disorders
35. Complementation Analysis of Peroxisomal Diseases: Kinetics of Assembly of Peroxisomes After Fusion of Complementary Cell Lines from Patients Deficient in Peroxisomes
36. Biochemical Analysis in Peroxisomal Disorders
37. Impaired Cholesterol Side Chain Cleavage Activity in Liver from Patients with the Cerebro-Hepato-Renal (Zellweger) Syndrome in Relation to the Accumulation of Di- and Trihydroxycoprostanoic Acid in Serum
38. Tyrosinaemia Type I: Orthotopic Liver Transplantation as the Only Definitive Answer to a Metabolic as well as an Oncological Problem
39. Prenatal and Perinatal Diagnosis of Peroxisomal Disorders
40. Acyclovir for varicella in immunocompetent patients
41. Leerboek Kindergeneeskunde, 2e geheel herz. dr
42. Bloedziekten
43. Tropische kindergneeskunde
44. Peroxisomal Abnormalities in Rhizomelic Chondrodysplasia Punctata
45. No association between transient hypothyroxinemia of prematurity and neurodevelopmental outcome in young adulthood
46. No association between transient hypothyroxinemia of prematurity and neurodevelopmental outcome in young adulthood
47. Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome
48. A milder variant of Zellweger syndrome
49. A sibship with a mild variant of Zellweger syndrome
50. Peroxisomal disorders: A newly recognised group of genetic diseases
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