Prof. Dr. med. Joachim Wölfle

Lehrstuhl für Kinder- und Jugendmedizin

Predictors of transient congenital primary hypothyroidism: data from the German registry for congenital hypothyroidism (AQUAPE “HypoDok”) (2021) Matejek N, Tittel SR, Haberland H, Rohrer T, Busemann EM, Jorch N, Schwab KO, et al. Journal article Previous diabetic ketoacidosis as a risk factor for recurrence in a large prospective contemporary pediatric cohort: Results from the DPV initiative (2021) Hammersen J, Tittel SR, Warncke K, Fritsch M, Placzek K, Pacaud D, Karges B, et al. Journal article Birthweight Differences in Adolescent Monozygotic Twins Influence Androgens, Psychological Morbidity, and Health-Related Quality of Life (2021) Schmitz L, Schulte S, Stoffel-Wagner B, Bartmann P, Plamper M, Schreiner F, Wölfle J, Gohlke B Journal article 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 Early start of growth hormone is associated with positive effects on auxology and metabolism in Prader-Willi-syndrome (2020) Magill L, Laemmer C, Wölfle J, Fimmers R, Gohlke B Journal article A role for the alpha-8 integrin chain (itga8) in glomerular homeostasis of the kidney. (2020) Marek I, Hilgers KF, Rascher W, Wölfle J, Hartner A Journal article, Review article Influence of Prenatal Environment on Androgen Steroid Metabolism In Monozygotic Twins With Birthweight Differences (2020) Schulte S, Schreiner F, Plamper M, Kasner C, Gruenewald M, Bartmann P, Fimmers R, et al. Journal article How to administer near-infrared spectroscopy in critically ill neonates, infants, and children (2020) Bruns N, Moosmann J, Münch F, Dohna-Schwake C, Wölfle J, Cesnjevar R, Dittrich S, et al. Journal article Cerebral MRI and Clinical Findings in Children with PTEN Hamartoma Tumor Syndrome: Can Cerebral MRI Scan Help to Establish an Earlier Diagnosis of PHTS in Children? (2020) Plamper M, Born M, Gohlke B, Schreiner F, Schulte S, Splittstößer V, Wölfle J Journal 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