H Willgerodt

High prevalence of the H1069Q mutation in East German patients with Wilson disease: rapid detection of mutations by limited sequencing and phenotype–genotype analysis

Karel Caca, Péter Ferenci, Hans-Jürgen Kühn et al. · Journal of Hepatology · 2001 · 164 citations

Life Sciences, Genetics, Molecular Genetics +17

The prevalence of anti-thyroid peroxidase antibodies and autoimmune thyroiditis in children and adolescents in an iodine replete area

M Kabelitz, KP Liesenkötter, Barbara Stach et al. · European Journal of Endocrinology · 2003 · 110 citations

Medicine, Endocrinology, Pediatrics +17

Small thyroid volumes and normal iodine excretion in Berlin schoolchildren indicate full normalization of iodine supply

Klaus‐Peter Liesenkötter, A. Kiebler, Barbara Stach et al. · Experimental and Clinical Endocrinology & Diabetes · 2009 · 62 citations

Medicine, Child Health, Endocrinology +13

Pregnancies in patients with congenital adrenal hyperplasia with complete or almost complete impairment of 21-hydroxylase activity

W Hoepffner, Egbert Schulze, J Bennek et al. · Fertility and Sterility · 2004 · 62 citations · Full text

Medicine, Endocrinology, Obstetrics +9

Linkage of Familial Euthyroid Goiter to the Multinodular Goiter-1 Locus and Exclusion of the Candidate Genes Thyroglobulin, Thyroperoxidase, and Na+/I− Symporter*

Susanne Neumann, H Willgerodt, Frank Ackermann et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 52 citations · Full text

Life Sciences, Endocrinology, Genetics +12