702 results on '"WIT, J. M."'
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2. The Proxy Problem: Child Report versus Parent Report in Health-Related Quality of Life Research
3. Measuring Health-Related Quality of Life in Children: The Development of the TACQOL Parent Form
4. De predictieve validiteit van de Screeningsvragenlijst Stevig Ouderschap
5. Ways to Improve the Diagnosis of Growth Hormone Deficiency
6. Mild deficits in attentional control in patients with the IGSF1 deficiency syndrome
7. IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management
8. Experience with Biosynthetic Growth Hormone
9. Long-term effects of oxandrolone treatment in childhood on neurocognition, quality of life and social–emotional functioning in young adults with Turner syndrome
10. Mutation of the POU-Specific Domain of Pit-1 and Hypopituitarism Without Pituitary Hypoplasia
11. The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients
12. Preterm birth and later insulin resistance: effects of birth weight and postnatal growth in a population based longitudinal study from birth into adult life: Insulin resistance 19 years after preterm birth
13. Monozygous triplets discordant for transient neonatal diabetes mellitus and for imprinting of the TNDM differentially methylated region
14. Disturbances of growth and endocrine function after busulphan-based conditioning for haematopoietic stem cell transplantation during infancy and childhood
15. Quality of life in adults following bone marrow transplantation during childhood
16. La croissance des enfants nés prématurés
17. CLINICAL AND LABORATORY FEATURES OF IGSF1 DEFICIENCY IN MALES AND FEMALES: OP14
18. Acceptability of Liquid Human Growth Hormone (hGH) [Norditropin Simple Xx®] in Adults and Children with GH Deficiency and Children with Chronic Renal Disease
19. Zoutverlies en hyperkaliëmie bij een pasgeborene
20. Pubertal development and growth after total-body irradiation and bone marrow transplantation for haematological malignancies
21. Gremlin 1, frizzled-related protein, and Dkk-1 are key regulators of human articular cartilage homeostasis
22. Short Stature Associated with a Novel Heterozygous Mutation in the Insulin-Like Growth Factor 1 Gene
23. A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency
24. IGF-1 and IGF-1 SDS – fit for purpose?
25. Drug development for children: how adequate is the current European ethical guidance?
26. Measuring health-related quality of life in children: the development of the TACQOL parent form
27. The proxy problem: child report versus parent report in health-related quality of life research
28. De novo mutations of the growth hormone gene: an important cause of congenital isolated growth hormone deficiency?
29. Impact of the Exon 3-Deleted Growth Hormone (GH) Receptor Polymorphism on Baseline Height and the Growth Response to Recombinant Human GH Therapy in GH-Deficient (GHD) and Non-GHD Children with Short Stature: A Systematic Review and Meta-Analysis
30. Intelligence of very preterm or very low birthweight infants in young adulthood
31. No change in developmental outcome with incubator covers and nesting for very preterm infants in a randomised controlled trial
32. De richtlijn lengtegroei voor de jeugdgezondheidszorg.
33. Consensus Statement on the Diagnosis and Treatment of Children with Idiopathic Short Stature: A Summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop
34. Antenatal glucocorticoid treatment is not associated with long-term metabolic risks in individuals born before 32 weeks of gestation
35. Health-related quality of life of very preterm infants at 1 year of age after two developmental care-based interventions
36. Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis
37. Mental and motor development before and during growth hormone treatment in infants and toddlers with Prader–Willi syndrome
38. Developing evidence-based guidelines for referral for short stature
39. Catch-up growth after prolonged hypothyroidism
40. Parental experiences during the first period at the neonatal unit after two developmental care interventions
41. Growth hormone (GH) secretion and response to GH therapy after total body irradiation and haematopoietic stem cell transplantation during childhood
42. Thyroid hormone levels in children with Prader—Willi syndrome before and during growth hormone treatment
43. Novel Mutations in the Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Type 1 Causing Blomstrand Osteochondrodysplasia Types I and II
44. A Variable Degree of Intrauterine and Postnatal Growth Retardation in a Family with a Missense Mutation in the Insulin-Like Growth Factor I Receptor
45. The effect of oestrogen treatment on body proportions in constitutionally tall girls
46. Body proportions in individuals with Turner syndrome
47. GROWTH-REDUCTIVE THERAPY IN CHILDREN WITH MARFAN SYNDROME
48. Nationwide age references for sitting height, leg length, and sitting height/height ratio, and their diagnostic value for disproportionate growth disorders
49. Homozygous and Heterozygous Expression of a Novel Insulin-Like Growth Factor-I Mutation
50. Inleiding: Wetenschappelijk onderzoek in het Willem-Alexander Kinder- en Jeugdcentrum (W-A KJC) van het Leids universitair Medisch Centrum (LUMC)
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