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H Biebermann

Showing results (1-10 of 22) with videos related to

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Deutsche Medizinische Wochenschrift (1946)|February 27, 2014
[Thyroid hormone action beyond classical concepts. The priority programme "Thyroid Trans Act" (SPP 1629) of the German Research Foundation]D Führer, K Brix, H Biebermann
The Journal of Clinical Endocrinology and Metabolism|April 1, 1996
Transient congenital hypothyroidism and hyperthyrotropinemia: normal thyroid function and physical development at the ages of 6-14 yearsB Köhler, D Schnabel, H Biebermann, et al.
The New England Journal of Medicine|May 8, 1997
Congenital hypothyroidism caused by mutations in the thyrotropin-receptor geneH Biebermann, A Grüters, T Schöneberg, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1996
The gene for the thyrotropin receptor (TSHR) as a candidate gene for congenital hypothyroidism with thyroid dysgenesisH Krude, H Biebermann, W Göpel, et al.
Langenbeck'S Archives of Surgery|December 29, 2000
Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhoodH Biebermann, T Schöneberg, H Krude, et al.
Hormone Research|July 15, 2000
Molecular pathogenesis of neonatal hypothyroidismH Krude, H Biebermann, D Schnabel, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1997
Congenital hyperthyroidismH Krude, H Biebermann, H P Krohn, et al.
Pediatric Research|August 14, 1999
Severe congenital hypothyroidism due to a homozygous mutation of the betaTSH geneH Biebermann, K P Liesenkötter, M Emeis, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
The first activating TSH receptor mutation in transmembrane domain 1 identified in a family with nonautoimmune hyperthyroidismH Biebermann, T Schöneberg, C Hess, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidismH Biebermann, T Schöneberg, H Krude, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Deutsche Medizinische Wochenschrift (1946)|February 27, 2014
[Thyroid hormone action beyond classical concepts. The priority programme "Thyroid Trans Act" (SPP 1629) of the German Research Foundation]D Führer, K Brix, H Biebermann
The Journal of Clinical Endocrinology and Metabolism|April 1, 1996
Transient congenital hypothyroidism and hyperthyrotropinemia: normal thyroid function and physical development at the ages of 6-14 yearsB Köhler, D Schnabel, H Biebermann, et al.
The New England Journal of Medicine|May 8, 1997
Congenital hypothyroidism caused by mutations in the thyrotropin-receptor geneH Biebermann, A Grüters, T Schöneberg, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1996
The gene for the thyrotropin receptor (TSHR) as a candidate gene for congenital hypothyroidism with thyroid dysgenesisH Krude, H Biebermann, W Göpel, et al.
Langenbeck'S Archives of Surgery|December 29, 2000
Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhoodH Biebermann, T Schöneberg, H Krude, et al.
Hormone Research|July 15, 2000
Molecular pathogenesis of neonatal hypothyroidismH Krude, H Biebermann, D Schnabel, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1997
Congenital hyperthyroidismH Krude, H Biebermann, H P Krohn, et al.
Pediatric Research|August 14, 1999
Severe congenital hypothyroidism due to a homozygous mutation of the betaTSH geneH Biebermann, K P Liesenkötter, M Emeis, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
The first activating TSH receptor mutation in transmembrane domain 1 identified in a family with nonautoimmune hyperthyroidismH Biebermann, T Schöneberg, C Hess, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidismH Biebermann, T Schöneberg, H Krude, et al.
Pageof 3