549 results on '"Van Vliet, Guy"'
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2. Why Should Orchidopexy Be Performed in Congenital Hypogonadotropic Hypogonadism, and When?
3. Thyrotropin Screening of Newborns: Before or After 72 Hours of Life? Before Discharge or at Home?
4. Biochemical and molecular evaluation of thyroid gland disorders in children
5. Disorders of the Thyroid in the Newborn and Infant
6. Contributors
7. Worldwide Newborn Screening and Early Immunizations: Aligning Advances in Preventive Pediatrics
8. Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
9. Newborn screening for congenital hypothyroidism and phenylketonuria—Beyond cost savings
10. Practical Endocrinology and Diabetes in Children
11. Neonatal Screening for Congenital Hypothyroidism: What It Has Taught us About Thyroid and Brain Development
12. Why should orchidopexy be performed in congenital hypogonadotropic hypogonadism, and when?
13. Transcriptomic signature of human embryonic thyroid reveals transition from differentiation to functional maturation
14. Similar age-dependent levothyroxine requirements of schoolchildren with congenital or acquired hypothyroidism
15. Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis
16. Molecular Mechanisms of Thyroid Gland Development : Insights from Clinical Studies and from Mutant Mice
17. Population-based TSH Screening of Newborns for Hyperthyroidism: It May Be Feasible, but Is It Justified?
18. List of Contributors
19. Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism
20. Decreasing Sex Difference in Birth Weight
21. Meeting Report: Measuring Endocrine-Sensitive Endpoints within the First Years of Life
22. Partnering with parents to disclose Klinefelter syndrome to their child
23. 8 - Disorders of the Thyroid in the Newborn and Infant
24. Chapter 10 - Biochemical and molecular evaluation of thyroid gland disorders in children
25. Diagnosis, Treatment and Outcome of Congenital Hypothyroidism
26. Transcriptomic Signature of Human Embryonic Thyroid Reveals Transition From Differentiation to Functional Maturation
27. Dépistage néonatal de l’hypothyroïdie congénitale et de l’hyperplasie congénitale des surrénales
28. Contributors
29. Newborn screening for congenital hypothyroidism and congenital adrenal hyperplasia : the balance of benefits and costs of a public health success
30. Transcriptomic signature of human embryonic thyroid reveals transition from differentiation to functional maturation.
31. The changing epidemiology of congenital hypothyroidism: fact or artifact?
32. Role for Tissue-Dependent Methylation Differences in the Expression of FOXE1 in Nontumoral Thyroid Glands
33. European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism
34. Whole-exome sequencing: opportunities in pediatric endocrinology
35. Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis
36. Redefining Congenital Hypothyroidism?
37. Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention
38. Thyroid Function from Birth to Adolescence in Prader-Willi Syndrome
39. FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly
40. PHARMACOTHERAPY: Treating congenital hypothyroidism —which levothyroxine?
41. Bioinactive ACTH Causing Glucocorticoid Deficiency
42. Lowering Thyrotropin Cutoff for Newborn Screening: Additional Cases of Congenital Hypothyroidism Are Identified, but What Do They Really Have?
43. Can Recovery from Hypothalamic-Pituitary-Adrenal (HPA) Axis Suppression Following Supraphysiological Doses of Glucocorticoids Be Predicted?
44. Leydig Cell Tumors in Children: Contrasting Clinical, Hormonal, Anatomical, and Molecular Characteristics in Boys and Girls
45. Developmental Abnormalities of the Thyroid
46. Congenital hypothyroidism: From paracelsus to molecular diagnosis
47. Contributors
48. A High Prevalence of Dual Thyroid Ectopy in Congenital Hypothyroidism: Evidence for Insufficient Signaling Gradients during Embryonic Thyroid Migration or for the Polyclonal Nature of the Thyroid Gland?
49. Muscle-Bone Characteristics in Children with Prader-Willi Syndrome
50. Severe Cortisol Deficiency Associated with Reversible Growth Hormone Deficiency in Two Infants: What Is the Link?
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