Matthias Viemann

Congenital Adrenal Hypoplasia: Clinical Spectrum, Experience with Hormonal Diagnosis, and Report on New Point Mutations of the DAX-1 Gene

Michael Peter, Matthias Viemann, Carl‐Joachim Partsch et al. · The Journal of Clinical Endocrinology & Metabolism · 1998 · 147 citations · Full text

Medicine, Endocrinology, Genetics +17

Management of Congenital Adrenal Hyperplasia: Results of the ESPE Questionnaire

Felix G. Riepe, Nils Krone, Matthias Viemann et al. · Hormone Research in Paediatrics · 2002 · 68 citations

Medicine, Endocrinology, Pediatrics +5

Elucidating the Underlying Molecular Pathogenesis of<i>NR3C2</i>Mutants Causing Autosomal Dominant Pseudohypoaldosteronism Type 1

Felix G. Riepe, Johannes Finkeldei, Luisa De Sanctis et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 65 citations · Full text

Medicine, Endocrinology, Molecular Genetics +17

Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1: Identification of a Novel Mutation in the Human Mineralocorticoid Receptor in one Sporadic Case and No Mutations in Two Autosomal Dominant Kindreds

Matthias Viemann, Michael Peter, Juan Pedro López-Siguero et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 62 citations

Life Sciences, Genetics, Molecular Genetics +14

Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1: Identification of a Novel Mutation in the Human Mineralocorticoid Receptor in one Sporadic Case and No Mutations in Two Autosomal Dominant Kindreds

Matthias Viemann · The Journal of Clinical Endocrinology & Metabolism · 2001 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14