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December 29, 2017
Mast Cell Activation Syndrome
Owen N Kramer, Marla S Barkoff, Claudia Hernandez
Fertility and Sterility
|
August 13, 2018
Maternal antithyroid antibodies and euploid miscarriage in women with recurrent early pregnancy loss
Shirley Cueva, Channing Burks, Dana McQueen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 7, 2010
Autoimmunity in patients with resistance to thyroid hormone
Marla S Barkoff, Masha Kocherginsky, João Anselmo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2009
Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community
Yardena Tenenbaum-Rakover, Helmut Grasberger, Sunee Mamanasiri, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 15, 2011
The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation
Chutintorn Sriphrapradang, Yardena Tenenbaum-Rakover, Mia Weiss, et al.
The Journal of Allergy and Clinical Immunology
|
September 3, 2019
AAAAI Mast Cell Disorders Committee Work Group Report: Mast cell activation syndrome (MCAS) diagnosis and management
Catherine R Weiler, K Frank Austen, Cem Akin, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Skinmed
|
December 29, 2017
Mast Cell Activation Syndrome
Owen N Kramer, Marla S Barkoff, Claudia Hernandez
Fertility and Sterility
|
August 13, 2018
Maternal antithyroid antibodies and euploid miscarriage in women with recurrent early pregnancy loss
Shirley Cueva, Channing Burks, Dana McQueen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 7, 2010
Autoimmunity in patients with resistance to thyroid hormone
Marla S Barkoff, Masha Kocherginsky, João Anselmo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2009
Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community
Yardena Tenenbaum-Rakover, Helmut Grasberger, Sunee Mamanasiri, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 15, 2011
The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation
Chutintorn Sriphrapradang, Yardena Tenenbaum-Rakover, Mia Weiss, et al.
The Journal of Allergy and Clinical Immunology
|
September 3, 2019
AAAAI Mast Cell Disorders Committee Work Group Report: Mast cell activation syndrome (MCAS) diagnosis and management
Catherine R Weiler, K Frank Austen, Cem Akin, et al.
Page
of 1