595 results on '"Wit, JM"'
Search Results
2. An analysis of intra-uterine growth retardation in rural Malawi
3. HeterozygousSTAT5bGene Mutations: Impact on Clinical Phenotype.
4. Short stature and the probability of coeliac disease, in the absence of gastrointestinal symptoms
5. Clinical and biochemical characteristics and bone mineral density of homozygous, compound heterozygous and heterozygous carriers of three novel IGFALS mutations.
6. Clinical and biochemical characteristics and bone mineral density of homozygous, compound heterozygous and heterozygous carriers of three novel IGFALS mutations.
7. Determinants of Advanced Bone Age in Childhood Obesity
8. Novel Leptin Receptor Mutations Identified in Two Girls with Severe Obesity Are Associated with Increased Bone Mineral Density
9. Mutations in TBL1X Are Associated With Central Hypothyroidism
10. Karyotype-Specific Ear and Hearing Problems in Young Adults With Turner Syndrome and the Effect of Oxandrolone Treatment
11. A randomized controlled trial of three years growth hormone and gonadotropin-releasing hormone agonist treatment in children with idiopathic short stature and intrauterine growth retardation
12. A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty
13. PAPSS2 Deficiency Causes Androgen Excess via Impaired DHEA Sulfation-In Vitro and in Vivo Studies in a Family Harboring Two Novel PAPSS2 Mutations
14. Adenomatous polyposis coli-mediated control of beta-catenin is essential for both chondrogenic and osteogenic differentiation of skeletal precursors
15. Successful long-term growth hormone therapy in a girl with haploinsufficiency of the insulin-like growth factor-1 receptor due to a terminal 15q26.2>qter deletion detected by multiplex ligation probe amplification
16. The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
17. Een stroomdiagram voor de diagnostiek van acute, niet traumatische gewrichtsklachten op de kinderleeftijd, retrospectief toegepast bij 115 kinderen
18. Pubertal development in the Netherlands
19. A nationwide cohort study on Creutzfeldt-Jacob disease among human growth hormone recipients
20. Efficacy of long-term growth hormone treatment in Turner's syndrome
21. Comments: A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty
22. Some Patients with Idiopathic Short Stature See Their Short Stature as a Problem but Others Do Not: Why this difference?
23. Should blood gas analysis be part of the diagnostic workup of short children? Auxological data and blood gas analysis in children with renal tubular acidosis
24. The diagnostic workup of growth failure in secondary health care; An evaluation of consensus guidelines
25. Klinisch geneesmiddelenonderzoek bij kinderen: nieuwe internationale richtlijnen
26. Loss-of-function mutations in the immunoglobulin superfamily member 1 gene (IGSF1) cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement
27. Referral patterns of children with poor growth in primary health care
28. Het gebruik van humaan hypofysair groeihormoon en het optreden van de ziekte van Creutzfeldt-Jakob. Een retro-spectieve cohortstudie in Nederland
29. Yearly stepwise increments of the growth hormone dose results in a better growth response after four years in girls with Turner syndrome
30. Impaired social status of growth hormone deficient adults as compared to controls with short or normal stature
31. CATCH-UP GROWTH IN 60 CHILDREN WITH CELIAC-DISEASE
32. RESULTS OF LONG-TERM THERAPY WITH GROWTH-HORMONE IN 2 DOSE REGIMENS IN TURNER SYNDROME
33. The effect of pubertal delay by GnRH agonist in GH-deficient children on final height
34. Parental experiences during the first period at the neonatal unit after two developmental care interventions
35. Psychosocial, cognitive, and motor functioning in patients with suspected Sotos syndrome: a comparison between patients with and without NSD1 gene alterations
36. Neonatal screening for congenital adrenal hyperplasia
37. Clinicians' perspective on quality of life assessment in paediatric clinical practice
38. Mutations in the NSD1 gene in patients with Sotos syndrome associate with endocrine and paracrine alterations in the IGF system
39. Benefit of postponing normal puberty for improving final height
40. Height, weight, body mass index and pubertal development references for children of Moroccan origin in The Netherlands
41. Expression of estrogen receptors and enzymes involved in sex steroid metabolism in the rat tibia during sexual maturation
42. Behaviour at 2 years of age in very preterm infants (gestational age <32 weeks)
43. Evidence for genomic and nongenomic actions of estrogen in growth plate regulation in female and male rats at the onset of sexual maturation
44. Reference values for height, height velocity and weight in Turner's Syndrome
45. Restricted catch-up growth after cessation of steroid treatment in a growth-hormone-deficient child
46. A special case of congenital adrenal hypoplasia and acute bilateral infantile striatal necrosis
47. A mathematical model describing catch-up growth in celiac disease
48. Effect of growth hormone treatment on craniofacial growth in Turner's syndrome
49. Aromatase inhibitors in pediatrics.
50. Inhibition of Gsk3β in cartilage induces osteoarthritic features through activation of the canonical Wnt signaling pathway.
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