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

Spermatogenesis, Comparative Endocrinology, Genetics +29

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

Developmental Biology, Congenital Hyperthyroidism, Genetics +9

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

Signal Transduction, Constitutive Activation, Oncogenic Agent +14

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

Endogenous Tsh Receptor, Signal Transduction, Human Tsh Receptor +8

Thyroid nodules in recurrent multinodular goiters are predominantly polyclonal

P. Harrer, M. Broecker, Antje Zint et al. · Journal of Endocrinological Investigation · 1998 · 37 citations

Iodine Deficiency Disorders, Thyroid Disease, Histopathology +1