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S Refetoff

Showing results (201-210 of 271) with videos related to

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The Journal of Clinical Investigation|April 16, 1998
Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice siteJ Pohlenz, I M Rosenthal, R E Weiss, et al.
Biochemical and Biophysical Research Communications|November 7, 1977
Reduced nuclear triiodothyronine receptors in starvation-induced hypothyroidismL J DeGroot, A H Coleoni, P A Rue, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type IP E Macchia, H H Harrison, N H Scherberg, et al.
Molecular Endocrinology (Baltimore, Md.)|March 1, 1992
An additional carbohydrate chain in the variant thyroxine-binding globulin-Gary (TBGAsn-96) impairs its secretionF Kambe, H Seo, Y Mori, et al.
Biochemical and Biophysical Research Communications|December 6, 1997
Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter geneJ Pohlenz, G Medeiros-Neto, J L Gross, et al.
Journal of Endocrinological Investigation|July 6, 2004
A novel splice variant involving the 5' untranslated region of thyroid hormone receptor beta1 (TRbeta1)D Mannavola, L C Moeller, P Beck-Peccoz, et al.
The Journal of Clinical Endocrinology and Metabolism|May 20, 1998
Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defectT Sunthornthepvarakul, S Likitmaskul, S Ngowngarmratana, et al.
Endocrinology|August 1, 1990
Effect of total sleep deprivation on 5'-deiodinase activity of rat brown adipose tissueS Balzano, B M Bergmann, M A Gilliland, et al.
Thyroid : Official Journal of the American Thyroid Association|January 26, 2000
A novel point mutation in cluster 3 of the thyroid hormone receptor beta gene (P247L) causing mild resistance to thyroid hormoneJ Pohlenz, L Manders, P M Sadow, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1996
A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center studyS Refetoff, V S Marinov, H Tunca, et al.
Pageof 28

Showing results (201-210 of 271) with videos related to

Sort By:
Pageof 28
The Journal of Clinical Investigation|April 16, 1998
Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice siteJ Pohlenz, I M Rosenthal, R E Weiss, et al.
Biochemical and Biophysical Research Communications|November 7, 1977
Reduced nuclear triiodothyronine receptors in starvation-induced hypothyroidismL J DeGroot, A H Coleoni, P A Rue, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type IP E Macchia, H H Harrison, N H Scherberg, et al.
Molecular Endocrinology (Baltimore, Md.)|March 1, 1992
An additional carbohydrate chain in the variant thyroxine-binding globulin-Gary (TBGAsn-96) impairs its secretionF Kambe, H Seo, Y Mori, et al.
Biochemical and Biophysical Research Communications|December 6, 1997
Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter geneJ Pohlenz, G Medeiros-Neto, J L Gross, et al.
Journal of Endocrinological Investigation|July 6, 2004
A novel splice variant involving the 5' untranslated region of thyroid hormone receptor beta1 (TRbeta1)D Mannavola, L C Moeller, P Beck-Peccoz, et al.
The Journal of Clinical Endocrinology and Metabolism|May 20, 1998
Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defectT Sunthornthepvarakul, S Likitmaskul, S Ngowngarmratana, et al.
Endocrinology|August 1, 1990
Effect of total sleep deprivation on 5'-deiodinase activity of rat brown adipose tissueS Balzano, B M Bergmann, M A Gilliland, et al.
Thyroid : Official Journal of the American Thyroid Association|January 26, 2000
A novel point mutation in cluster 3 of the thyroid hormone receptor beta gene (P247L) causing mild resistance to thyroid hormoneJ Pohlenz, L Manders, P M Sadow, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1996
A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center studyS Refetoff, V S Marinov, H Tunca, et al.
Pageof 28