Joachim Wölfle

Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes

Violeta Mihaylova, Juliane S. Müller, Juan J. Vílchez et al. · Brain · 2008 · 160 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Basal Inhibin B and the Testosterone Response to Human Chorionic Gonadotropin Correlate in Prepubertal Boys¹

K. Kubini, M. Zachmann, Norbert Albers et al. · The Journal of Clinical Endocrinology & Metabolism · 2000 · 96 citations · Full text

Medicine, Endocrinology, Pediatrics +17

Microvascular Complications in Childhood-Onset Type 1 Diabetes and Celiac Disease: A Multicenter Longitudinal Analysis of 56,514 Patients From the German-Austrian DPV Database

Tilman Rohrer, Johannes Wolf, Susanne Liptay et al. · Diabetes Care · 2015 · 96 citations

Medicine, Internal Medicine, Diabetology +14

Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counselling

F. Haverkamp, Joachim Wölfle, M. Aretz et al. · European Journal of Pediatrics · 1999 · 66 citations

Medicine, Genetics, Pediatrics +15

Treatment of young patients with HNF1A mutations (HNF1A–MODY)

Klemens Raile, Edith Schober, Katja Konrad et al. · Diabetic Medicine · 2014 · 49 citations · Full text

Medicine, Endocrinology, Molecular Genetics +17