Prof. Dr. Helmuth-Günther Dörr

Medizinische Fakultät Professur für Kinderheilkunde mit dem Schwerpunkt Kinder-Endokrinologie und Diabetologie

Sex chromosome DSD individuals with mosaic 45,X0 and aberrant Y chromosomes in 46,XY cells: distinct gender phenotypes and germ cell tumour risks§ (2022) Vogt PH, Besikoglu B, Bettendorf M, Frank-Herrmann P, Zimmer J, Bender U, Knauer-Fischer S, et al. Journal article Effect of Psychosocial Factors on Growth (2021) Gohlke BC, Bettendorf M, Binder G, Hauffa B, Reinehr T, Dörr HG, Wölfle J Journal article Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21-hydroxylase deficiency in Europe (2021) Nowotny HF, Neumann U, Tardy-Guidollet V, Ahmed SF, Baronio F, Battelino T, Bertherat J, et al. Conference contribution Safety and effectiveness of pediatric growth hormone therapy: Results from the full cohort in KIGS (2021) Maghnie M, Ranke MB, Geffner ME, Vlachopapadopoulou E, Dörr HG, Wikland KA, Ibanez L, et al. Conference contribution Recombinant Human Growth Hormone Activates Neuroprotective Growth Factors in Hypoxic Brain Injury in Neonatal Mice (2021) Jung S, Terörde K, Dörr HG, Trollmann R Journal article Das nicht klassische Adrenogenitale Syndrom mit 21-Hydroxylase-Defekt bei Kindern und Jugendlichen (2021) Dörr HG, Schulze N Journal article Hydrocortisone dosing in children with classic congenital adrenal hyperplasia: Results of the german/austrian registry (2021) Hoyer-Kuhn H, Huebner A, Richter-Unruh A, Bettendorf M, Rohrer T, Kapelari K, Riedl S, et al. Journal article Mono-allelic deleterious variants in autosomal recessive skeletal dysplasia genes are strongly associated with idiopathic short stature (2020) Thiel CT, Hauer N, Vogl C, Uebe S, Sticht H, Ekici AB, Kraus C, et al. Conference contribution Evolving pituitary hormone deficits in primarily isolated GHD: a review and experts' consensus. (2020) Binder G, Schnabel D, Reinehr T, Pfaeffle R, Dörr HG, Bettendorf M, Hauffa BP, Wölfle J Journal article, Review article Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. (2020) Dörr HG, Schulze N, Bettendorf M, Binder G, Bonfig W, Denzer C, Dunstheimer D, et al. Journal article