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Steroid-induced diabetes: a clinical and molecular approach to understanding and treatment.
- Published in:
- Diabetes/Metabolism Research & Reviews, 2014, v. 30, n. 2, p. 96, doi. 10.1002/dmrr.2486
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- Publication type:
- Article
Mice deficient in the steroid receptor co-activator 1 (SRC-1) are resistant to thyroid hormone.
- Published in:
- EMBO Journal, 1999, v. 18, n. 7, p. 1900, doi. 10.1093/emboj/18.7.1900
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- Publication type:
- Article
Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations.
- Published in:
- 2020
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- Publication type:
- journal article
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
- Published in:
- 2019
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- Publication type:
- journal article
Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Effects of ligand and thyroid hormone receptor isoforms on hepatic gene expression profiles of thyroid hormone receptor knockout mice.
- Published in:
- EMBO Reports, 2003, v. 4, n. 6, p. 581, doi. 10.1038/sj.embor.embor862
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- Publication type:
- Article
Automation of mass vaccination against COVID-19 at an academic health center.
- Published in:
- JAMIA Open, 2021, v. 4, n. 4, p. 1, doi. 10.1093/jamiaopen/ooab102
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- Publication type:
- Article
Neonatal Detection of Generalized Resistance to Thyroid Hormone.
- Published in:
- 1990
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- Publication type:
- Case Study
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.
- Published in:
- Nature Genetics, 2005, v. 37, n. 11, p. 1247, doi. 10.1038/ng1654
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- Publication type:
- Article
Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Fetal Exposure to High Maternal Thyroid Hormone Levels Causes Central Resistance to Thyroid Hormone in Adult Humans and Mice.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Diiodothyropropionic acid (DITPA) in the treatment of MCT8 deficiency.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.
- Published in:
- 2012
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- Publication type:
- journal article
Distinct and Histone-Specific Modifications Mediate Positive versus Negative Transcriptional Regulation of TSHα Promoter.
- Published in:
- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009853
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- Publication type:
- Article
Eyes on the Prize: Decoding the Ophthalmic Product Regulations and Intricacies of the U.S. Food and Drug Administration Approval.
- Published in:
- Journal of Ocular Pharmacology & Therapeutics, 2023, v. 39, n. 8, p. 572, doi. 10.1089/jop.2023.0071
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- Publication type:
- Article
Approach to the patient with resistance to thyroid hormone and pregnancy.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Autoimmunity in patients with resistance to thyroid hormone.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Sleep disturbances, daytime sleepiness, and quality of life in adults with growth hormone deficiency.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X).
- Published in:
- 2009
- By:
- Publication type:
- journal article
Assessment of Adrenal Reserve in Pregnancy: Defining the Normal Response to the Adrenocorticotropin Stimulation Test.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 10, p. 3866, doi. 10.1210/jc.2006-1049
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- Publication type:
- Article
Mosaicism of a Thyroid Hormone Receptor-β Gene Mutation in Resistance to Thyroid Hormone.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 9, p. 3471, doi. 10.1210/jc.2006-0727
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- Publication type:
- Article
A Novel Thyroid Hormone Receptor-β Mutation That Fails to Bind Nuclear Receptor Corepressor in a Patient as an Apparent Cause of Severe, Predominantly Pituitary Resistance to Thyroid Hormone.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 5, p. 1887, doi. 10.1210/jc.2005-2428
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- Publication type:
- Article
Autosomal Dominant Resistance to Thyrotropin as a Distinct Entity in Five Multigenerational Kindreds: Clinical Characterization and Exclusion of Candidate Loci.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 7, p. 4025, doi. 10.1210/jc.2005-0572
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- Publication type:
- Article
A De Novo Mutation in an Already Mutant Nucleotide of the Thyroid Hormone Receptor β Gene Perpetuates Resistance to Thyroid Hormone.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 3, p. 1760, doi. 10.1210/jc.2004-1488
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- Publication type:
- Article
Effect of Pioglitazone on Adrenocorticotropic Hormone and Cortisol Secretion in Cushing's Disease.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 3, p. 1340, doi. 10.1210/jc.2004-1746
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- Publication type:
- Article
Resistance to Thyroid Hormone Does Not Abrogate the Transient Thyrotoxicosis Associated with Gestation: Report of a Case.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 9, p. 4273, doi. 10.1210/jcem.86.9.7858
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- Publication type:
- Article
Search for Abnormalities of Nuclear Corepressors, Coactivators, and a Coregulator in Families with Resistance to Thyroid Hormone without Mutations in Thyroid Hormone Receptor β or α Genes.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 10, p. 3609, doi. 10.1210/jcem.85.10.6873
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- Publication type:
- Article
Failure of Membrane Targeting Causes the Functional Defect of Two Mutant Sodium Iodide Symporters.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 7, p. 2366, doi. 10.1210/jcem.85.7.6700
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- Publication type:
- Article
Five New Families with Resistance to Thyroid Hormone not Caused by Mutations in the Thyroid Hormone Receptor β Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 11, p. 3919, doi. 10.1210/jcem.84.11.6080
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- Publication type:
- Article
Two Different Mutations in the Thyroid Peroxidase Gene of a Large Inbred Amish Kindred: Power and Limits of Homozygosity Mapping.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 3, p. 1061, doi. 10.1210/jcem.84.3.5541
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- Publication type:
- Article
Editorial: Treatment of Resistance to Thyroid Hormone—Primum Non Nocere.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 2, p. 401, doi. 10.1210/jcem.84.2.5534
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- Publication type:
- Article
Complete Thyroxine-Binding Globulin (TBG) Deficiency Produced by a Mutation in Acceptor Splice Site Causing Frameshift and Early Termination of Translation (TBG-Kankakee).
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 10, p. 3604, doi. 10.1210/jcem.83.10.5208
- By:
- Publication type:
- Article
Resistance to Thyrotropin (TSH) in Three Families Is not Associated with Mutations in the TSH Receptor or TSH.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1997, v. 82, n. 12, p. 3933, doi. 10.1210/jcem.82.12.4418
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- Publication type:
- Article
Abnormalities in the biosynthesis of cartilage and bone proteoglycans in experimental diabetes.
- Published in:
- 1981
- By:
- Publication type:
- journal article
Medical Mimics.
- Published in:
- Annals of the New York Academy of Sciences, 2001, v. 931, n. 1, p. 97, doi. 10.1111/j.1749-6632.2001.tb05775.x
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- Publication type:
- Article
Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
- Published in:
- Thyroid, 2023, v. 33, n. 2, p. 261, doi. 10.1089/thy.2022.0492
- By:
- Publication type:
- Article
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism.
- Published in:
- Thyroid, 2021, v. 31, n. 10, p. 1589, doi. 10.1089/thy.2021.0210
- By:
- Publication type:
- Article
Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency.
- Published in:
- Thyroid, 2021, v. 31, n. 9, p. 1316, doi. 10.1089/thy.2020.0696
- By:
- Publication type:
- Article
Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor α Gene (pC380SfsX9) Mutation.
- Published in:
- Thyroid, 2021, v. 31, n. 6, p. 1003, doi. 10.1089/thy.2020.0695
- By:
- Publication type:
- Article
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation.
- Published in:
- Thyroid, 2021, v. 31, n. 5, p. 713, doi. 10.1089/thy.2020.0306
- By:
- Publication type:
- Article
Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism.
- Published in:
- Thyroid, 2020, v. 30, n. 5, p. 780, doi. 10.1089/thy.2019.0636
- By:
- Publication type:
- Article
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 Variants.
- Published in:
- Thyroid, 2020, v. 30, n. 3, p. 463, doi. 10.1089/thy.2018.0703
- By:
- Publication type:
- Article
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families.
- Published in:
- Thyroid, 2019, v. 29, n. 2, p. 302, doi. 10.1089/thy.2018.0295
- By:
- Publication type:
- Article
A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism.
- Published in:
- Thyroid, 2018, v. 24, n. 8, p. 1068, doi. 10.1089/thy.2018.0137
- By:
- Publication type:
- Article
Adeno Associated Virus 9-Based Gene Therapy Delivers a Functional Monocarboxylate Transporter 8, Improving Thyroid Hormone Availability to the Brain of Mct8-Deficient Mice.
- Published in:
- Thyroid, 2016, v. 26, n. 9, p. 1311, doi. 10.1089/thy.2016.0060
- By:
- Publication type:
- Article
Intractable Early Childhood Obesity as the Initial Sign of Insulin Resistant Hyperinsulinism and Precursor of Polycystic Ovary Syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2007, v. 20, n. 1, p. 41
- By:
- Publication type:
- Article
Mineralocorticoid insufficiency due to suramin therapy.
- Published in:
- 1996
- By:
- Publication type:
- journal article
Impact of GH replacement therapy on sleep in adult patients with GH deficiency of pituitary origin.
- Published in:
- European Journal of Endocrinology, 2013, v. 168, n. 5, p. 763, doi. 10.1530/EJE-12-1037
- By:
- Publication type:
- Article
Fetal Loss Associated With Excess Thyroid Hormone Exposure.
- Published in:
- 2005
- By:
- Publication type:
- Letter
Fetal Loss Associated With Excess Thyroid Hormone Exposure.
- Published in:
- JAMA: Journal of the American Medical Association, 2004, v. 292, n. 6, p. 691, doi. 10.1001/jama.292.6.691
- By:
- Publication type:
- Article