Prof. Dr. Helmuth-Günther Dörr



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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

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 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 Das nicht klassische Adrenogenitale Syndrom mit 21-Hydroxylase-Defekt bei Kindern und Jugendlichen (2021) Dörr HG, Schulze N 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 Ektope Lage einer Schilddrüse im Zungengrund – Zufallsdiagnose bei einem 6‑jährigen Mädchen (2020) Albrecht A, Penger T, Marx M, Jüngert JM, Kuwert T, Dörr HG Journal article Malformationen des Zentralnervensystems: Seltene Ursachen eines organischen Wachstumshormonmangels bei Kindern (2020) Dörr HG, Bettendorf M, Binder G, Hauffa B, Mohnike K, Mueller HL, Reinehr T, et al. Journal article