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Clinical Endocrinology|September 30, 2000
Functional characterization of five constitutively activating thyrotrophin receptor mutationsP Wonerow, S Chey, D Führer, et al.
European Journal of Medical Research|July 25, 1996
Constitutively activating mutations of the thyrotropin receptor and thyroid diseaseD Führer, H P Holzapfel, P Wonerow, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 4, 2001
Detection of thyroid-stimulating hormone receptor and Gsalpha mutations: in 75 toxic thyroid nodules by denaturing gradient gel electrophoresisB Trülzsch, K Krohn, P Wonerow, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Somatic mutations in the thyrotropin receptor gene and not in the Gs alpha protein gene in 31 toxic thyroid nodulesD Führer, H P Holzapfel, P Wonerow, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Identification of constitutively activating somatic thyrotropin receptor mutations in a subset of toxic multinodular goitersH P Holzapfel, D Führer, P Wonerow, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 29, 1998
Autosomal dominant nonautoimmune hyperthyroidism. Clinical features-diagnosis-therapyD Führer, M Mix, H Willgerodt, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidismD Führer, P Wonerow, H Willgerodt, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 1998
Clonal origin of toxic thyroid nodules with constitutively activating thyrotropin receptor mutationsK Krohn, D Führer, H P Holzapfel, et al.
Thyroid : Official Journal of the American Thyroid Association|September 11, 1999
Variable phenotype associated with Ser505Asn-activating thyrotropin-receptor germline mutationD Führer, M Mix, P Wonerow, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Sporadic congenital hyperthyroidism due to a spontaneous germline mutation in the thyrotropin receptor geneH P Holzapfel, P Wonerow, W von Petrykowski, et al.
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