M. Broecker

Impact of Estrogen Replacement Therapy in a Male with Congenital Aromatase Deficiency Caused by a Novel Mutation in the CYP19 Gene

Burkhard L. Herrmann, Bernhard Saller, Peter Gocke et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 230 citations

Life Sciences, Endocrinology, Genetics +17

Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism

Karl‐Otfried Schwab, M. Gerlich, M. Broecker et al. · The Journal of Pediatrics · 1997 · 50 citations

Medicine, Endocrinology, Genetics +10

Constitutive activation of the Gs alpha protein-adenylate cyclase pathway may not be sufficient to generate toxic thyroid adenomas.

Michael Derwahl, C Hamacher, Diego Russo et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 46 citations · Full text

Life Sciences, Endocrinology, Genetics +15

Expression of the Human TSH Receptor in a Human Thyroid Carcinoma Cell Line That Lacks an Endogenous TSH Receptor: Growth Inhibition by cAMP

Michael Derwahl, M. Kuemmel, Peter E. Goretzki et al. · Biochemical and Biophysical Research Communications · 1993 · 38 citations

Medicine, Endocrinology, Molecular Biology +14

Thyroid nodules in recurrent multinodular goiters are predominantly polyclonal

P. Harrer, M. Broecker, Antje Zint et al. · Journal of Endocrinological Investigation · 1998 · 38 citations

Medicine, Endocrinology, Radiology +11