Detalhe da pesquisa
1.
Graves' disease and papillary thyroid carcinoma: case report and literature review of a single academic center.
BMC Endocr Disord
; 22(1): 199, 2022 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35945543
2.
The syndromes of reduced sensitivity to thyroid hormone.
Biochim Biophys Acta
; 1830(7): 3987-4003, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22986150
3.
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.
Nat Genet
; 37(11): 1247-52, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16228000
4.
STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179.
Nat Genet
; 56(5): 877-888, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38714869
5.
Effect of the Fetal THRB Genotype on the Placenta.
J Clin Endocrinol Metab
; 108(10): e944-e948, 2023 09 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37149816
6.
A Novel Pathogenic Variant in PAX8 Leads to Familial Congenital Hypothyroidism.
Thyroid
; 32(8): 1000-1002, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35611983
7.
Extended Absorption of Liothyronine from Poly-Zinc-Liothyronine: Results from a Phase 1, Double-Blind, Randomized, and Controlled Study in Humans.
Thyroid
; 32(2): 196-205, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34641706
8.
Severe Resistance to Thyroid Hormone Beta in a Patient with Athyreosis.
Thyroid
; 32(3): 336-339, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34969265
9.
AAV9-MCT8 Delivery at Juvenile Stage Ameliorates Neurological and Behavioral Deficits in a Mouse Model of MCT8-Deficiency.
Thyroid
; 32(7): 849-859, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35350867
10.
Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor α Gene (pC380SfsX9) Mutation.
Thyroid
; 31(6): 1003-1005, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33198587
11.
Dietary Selenium Deficiency Partially Mimics the Metabolic Effects of Arsenic.
Nutrients
; 13(8)2021 Aug 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34445052
12.
Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone Metabolism.
Thyroid
; 31(2): 202-207, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32718224
13.
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation.
Thyroid
; 31(5): 713-720, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32746752
14.
Role of the Thyroid Gland in Expression of the Thyroid Phenotype of Sbp2-Deficient Mice.
Endocrinology
; 161(5)2020 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31826256
15.
Nonautoimmune Hyperthyroidism Caused by a Somatic Mosaic GNAS Mutation Involving Part of the Thyroid Gland.
Thyroid
; 30(4): 640-642, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31910104
16.
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 Variants.
Thyroid
; 30(3): 463-465, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31856685
17.
Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations.
J Clin Endocrinol Metab
; 105(3)2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32084277
18.
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
J Clin Endocrinol Metab
; 105(5)2020 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31867598
19.
Reduced Sensitivity to Thyroid Hormone as a Transgenerational Epigenetic Marker Transmitted Along the Human Male Line.
Thyroid
; 29(6): 778-782, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30938226
20.
Very Severe Resistance to Thyroid Hormone ß in One of Three Affected Members of a Family with a Novel Mutation in the THRB Gene.
Thyroid
; 29(10): 1518-1520, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31432759