Professur für Kinderheilkunde mit dem Schwerpunkt Kinder-Endokrinologie und Diabetologie (Stiftungsprofessur)

Caring for a Child with Congenital Adrenal Hyperplasia Diagnosed by Newborn Screening: Parental Health-Related Quality of Life, Coping Patterns, and Needs (2023) Rautmann L, Witt S, Theiding C, Odenwald B, Nennstiel-Ratzel U, Dörr HG, Quitmann JH Journal article Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe (2022) Nowotny H, Neumann U, Tardy-Guidollet V, Faisal Ahmed S, Baronio F, Battelino T, Bertherat J, et al. Journal article BDV Syndrome: An Emerging Syndrome with Profound Obesity and Neurodevelopmental Delay Resembling Prader-Willi Syndrome (2021) Bosch E, Hebebrand M, Popp B, Penger T, Behring B, Cox H, Towner S, et al. 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 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 Das nicht klassische adrenogenitale Syndrom mit 21-Hydroxylase-Defekt bei Kindern und Jugendlichen (2020) Dörr HG, Schulze N Journal article Genotyp-Phänotyp-Korrelationen bei Kindern und Jugendlichen mit nichtklassischem adrenogenitalen Syndrom mit 21-Hydroxylase-Defekt (2020) Dörr HG, Schulze N, Bettendorf M, Binder G, Bonfig W, Denzer C, Dunstheimer D, et al. Journal article