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1. Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development

2. CRH receptor antagonist crinecerfont – a promising new treatment option for patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

4. Cardiometabolic Aspects of Congenital Adrenal Hyperplasia

7. Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development

11. Hormonal control during infancy and testicular adrenal rest tumor development in CAH males - a retrospective multi-center cohort study

12. Quality of life in men with Klinefelter syndrome: a multicentre study

13. The clinical characteristics and quality of life of 248 pediatric and adult patients with Congenital Adrenal Hyperplasia

14. Corrigendum: Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country

16. A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency

17. Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country

20. Identification of a Novel CYP11B2 Variant in a Family with Varying Degrees of Aldosterone Synthase Deficiency

22. Transcriptional comparison of testicular adrenal rest tumors with fetal and adult tissues

23. The impact of Klinefelter syndrome on socioeconomic status: a multicenter study

24. Treatment of congenital adrenal hyperplasia in children aged 0–3 years: a retrospective\ud multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure

25. Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

26. Optimizing the Timing of Highest Hydrocortisone Dose in Children and Adolescents With 21-Hydroxylase Deficiency

27. Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency:Lessons from a developing country

28. Treatment of congenital adrenal hyperplasia in children aged 0–3 years:A retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure

29. Diurnal salivary androstenedione and 17-hydroxyprogesterone levels in healthy volunteers for monitoring treatment efficacy of patients with congenital adrenal hyperplasia

30. Optimizing the Timing of Highest Hydrocortisone Dose in Children and Adolescents With 21-Hydroxylase Deficiency

31. Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries

32. Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

33. Birth Weight in Different Etiologies of Disorders of Sex Development

36. Diurnal salivary androstenedione and 17‐hydroxyprogesterone levels in healthy volunteers for monitoring treatment efficacy of patients with congenital adrenal hyperplasia

38. Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries.

39. Optimizing the Timing of Highest Hydrocortisone Dose in Children and Adolescents With 21-Hydroxylase Deficiency

44. Real world estimates of adrenal insufficiency related adverse events in children with congenital adrenal hyperplasia

46. Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21-hydroxylase deficiency in Europe

47. International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia:Data from the I-CAH registry

48. Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands: A Newborn Screening Pilot Study

49. High Prevalence of Weight Gain in Childhood Brain Tumor Survivors and Its Association With Hypothalamic-Pituitary Dysfunction

50. International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia: Data from the I-CAH registry

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