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Communications Biology
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March 22, 2025
Extracellular phase separation mediates storage and release of thyroglobulin in the thyroid follicular lumen
Yihan Yao, Nadia Erkamp, Tomas Sneideris, et al.
Plos Computational Biology
|
April 18, 2017
Semantic prioritization of novel causative genomic variants
Imane Boudellioua, Rozaimi B Mahamad Razali, Maxat Kulmanov, et al.
Clinical Endocrinology
|
May 18, 2026
What Endocrinologists Should Know About Iodine: Population Deficiency, Individual Excess and Misinformation in the United Kingdom
Peter N Taylor, Malcolm Prentice, Sarah Bath, et al.
European Thyroid Journal
|
February 25, 2026
Iopanoic acid rapidly restores euthyroidism in refractory thyrotoxicosis pre-thyroidectomy: a retrospective study
Christine Newman, Muhammed Saqlain, Isra Ahmed Mohammed, et al.
The Journal of Clinical Investigation
|
February 9, 2016
Mutation in human selenocysteine transfer RNA selectively disrupts selenoprotein synthesis
Erik Schoenmakers, Bradley Carlson, Maura Agostini, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 13, 2012
Mitochondrial oxidative phosphorylation is impaired in patients with congenital lipodystrophy
Alison Sleigh, Anna Stears, Kerrie Thackray, et al.
The Lancet. Diabetes & Endocrinology
|
June 28, 2014
Resistance to thyroid hormone caused by a mutation in thyroid hormone receptor (TR)α1 and TRα2: clinical, biochemical, and genetic analyses of three related patients
Carla Moran, Maura Agostini, W Edward Visser, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 14, 2013
An adult female with resistance to thyroid hormone mediated by defective thyroid hormone receptor α
Carla Moran, Nadia Schoenmakers, Maura Agostini, et al.
Clinical Endocrinology
|
August 8, 2018
A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome
Edna F Roche, Anne McGowan, Olympia Koulouri, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 21, 2014
A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemia
Nadia Schoenmakers, Carla Moran, Irene Campi, et al.
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of 5
Search research articles
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Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
Communications Biology
|
March 22, 2025
Extracellular phase separation mediates storage and release of thyroglobulin in the thyroid follicular lumen
Yihan Yao, Nadia Erkamp, Tomas Sneideris, et al.
Plos Computational Biology
|
April 18, 2017
Semantic prioritization of novel causative genomic variants
Imane Boudellioua, Rozaimi B Mahamad Razali, Maxat Kulmanov, et al.
Clinical Endocrinology
|
May 18, 2026
What Endocrinologists Should Know About Iodine: Population Deficiency, Individual Excess and Misinformation in the United Kingdom
Peter N Taylor, Malcolm Prentice, Sarah Bath, et al.
European Thyroid Journal
|
February 25, 2026
Iopanoic acid rapidly restores euthyroidism in refractory thyrotoxicosis pre-thyroidectomy: a retrospective study
Christine Newman, Muhammed Saqlain, Isra Ahmed Mohammed, et al.
The Journal of Clinical Investigation
|
February 9, 2016
Mutation in human selenocysteine transfer RNA selectively disrupts selenoprotein synthesis
Erik Schoenmakers, Bradley Carlson, Maura Agostini, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 13, 2012
Mitochondrial oxidative phosphorylation is impaired in patients with congenital lipodystrophy
Alison Sleigh, Anna Stears, Kerrie Thackray, et al.
The Lancet. Diabetes & Endocrinology
|
June 28, 2014
Resistance to thyroid hormone caused by a mutation in thyroid hormone receptor (TR)α1 and TRα2: clinical, biochemical, and genetic analyses of three related patients
Carla Moran, Maura Agostini, W Edward Visser, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 14, 2013
An adult female with resistance to thyroid hormone mediated by defective thyroid hormone receptor α
Carla Moran, Nadia Schoenmakers, Maura Agostini, et al.
Clinical Endocrinology
|
August 8, 2018
A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome
Edna F Roche, Anne McGowan, Olympia Koulouri, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 21, 2014
A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemia
Nadia Schoenmakers, Carla Moran, Irene Campi, et al.
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of 5