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Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in Sao Paulo, Brazil

European journal of endocrinology, 2008-09, Vol.159 (3), p.293

2008

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Congenital hypothyroidism and thyroid cancer

Endocrine-related cancer, 2021-09, Vol.28 (9), p.R217-R230

2021

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Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors

The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.E944-E952

2014

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Sesquiterpene Lactones from Calea pinnatifida : Absolute Configuration and Structural Requirements for Antitumor Activity

Molecules (Basel, Switzerland), 2020-06, Vol.25 (13), p.3005

2020

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The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

The journal of clinical endocrinology and metabolism, 2009-08, Vol.94 (8), p.2938-2944

2009

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HOPX homeobox methylation in differentiated thyroid cancer and its clinical relevance

Endocrine Connections, 2018-12, Vol.7 (12), p.1333-1342

2018

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Association of Low Sodium-Iodide Symporter Messenger Ribonucleic Acid Expression in Malignant Thyroid Nodules with Increased Intracellular Protein Staining

The journal of clinical endocrinology and metabolism, 2008-10, Vol.93 (10), p.4141-4145

2008

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Mutations of the thyroglobulin gene and its relevance to thyroid disorders

Current opinion in endocrinology, diabetes, and obesity, 2009-10, Vol.16 (5), p.373-378

2009

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Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres

Clinical endocrinology (Oxford), 2004-03, Vol.60 (3), p.300-308

2004

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A novel system of genetic transformation allows multiple integrations of a desired gene in Saccharomyces cerevisiae chromosomes

Journal of microbiological methods, 2006-12, Vol.67 (3), p.437-445

2006

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Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations

Thyroid (New York, N.Y.), 2008-07, Vol.18 (7), p.783

2008

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High prevalence of side effects after recombinant human thyrotropin-stimulated radioiodine treatment with 30 mCi in patients with multinodular goiter and subclinical/clinical hyperthyroidism

Thyroid (New York, N.Y.), 2009-09, Vol.19 (9), p.945

2009

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Prolonged follow-up of multinodular goitre patients treated with radioiodine preceded or not by human recombinant TSH

Clinical endocrinology (Oxford), 2006-04, Vol.64 (4), p.474-474

2006

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The Prevalence of Thyroid Dysfunction in Elderly Cardiology Patients with Mild Excessive Iodine Intake in the Urban Area of São Paulo

Clinics (São Paulo, Brazil), 2009-02, Vol.64 (2), p.135-142

2009

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Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect

Thyroid (New York, N.Y.), 2003-12, Vol.13 (12), p.1145-1151

2003

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Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect

Arquivos brasileiros de endocrinologia e metabologia, 2010-11, Vol.54 (8), p.732-737

2010

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Human Recombinant TSH Preceding a Therapeutic Dose of Radioiodine for Multinodular Goiters Has No Significant Effect in the Surge of TSH-Receptor and TPO Antibodies

Thyroid (New York, N.Y.), 2005-02, Vol.15 (2), p.134-139

2005

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A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation

Arquivos brasileiros de endocrinologia e metabologia, 2008-11, Vol.52 (8), p.1337-1344

2008

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Lysicamine Reduces Protein Kinase B (AKT) Activation and Promotes Necrosis in Anaplastic Thyroid Cancer

Pharmaceuticals (Basel, Switzerland), 2023-12, Vol.16 (12), p.1687

2023

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Overexpression of Epidermal Growth Factor and Epidermal Growth Factor-Receptor mRNAs in Dyshormonogenetic Goiters

Thyroid (New York, N.Y.), 2001-01, Vol.11 (1), p.15-20

2001

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Hipotireoidismo Congênito: Recentes Avanços em Genética Molecular

Arquivos brasileiros de endocrinologia e metabologia, 2002-08, Vol.46 (4), p.391-401

2002

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Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in Sao Paulo, Brazil

Congenital hypothyroidism and thyroid cancer

Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors

Sesquiterpene Lactones from Calea pinnatifida : Absolute Configuration and Structural Requirements for Antitumor Activity

The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

HOPX homeobox methylation in differentiated thyroid cancer and its clinical relevance

Association of Low Sodium-Iodide Symporter Messenger Ribonucleic Acid Expression in Malignant Thyroid Nodules with Increased Intracellular Protein Staining

Mutations of the thyroglobulin gene and its relevance to thyroid disorders

Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres

A novel system of genetic transformation allows multiple integrations of a desired gene in Saccharomyces cerevisiae chromosomes

Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations

High prevalence of side effects after recombinant human thyrotropin-stimulated radioiodine treatment with 30 mCi in patients with multinodular goiter and subclinical/clinical hyperthyroidism

Prolonged follow-up of multinodular goitre patients treated with radioiodine preceded or not by human recombinant TSH

The Prevalence of Thyroid Dysfunction in Elderly Cardiology Patients with Mild Excessive Iodine Intake in the Urban Area of São Paulo

Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect

Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect

Human Recombinant TSH Preceding a Therapeutic Dose of Radioiodine for Multinodular Goiters Has No Significant Effect in the Surge of TSH-Receptor and TPO Antibodies

A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation

Lysicamine Reduces Protein Kinase B (AKT) Activation and Promotes Necrosis in Anaplastic Thyroid Cancer

Overexpression of Epidermal Growth Factor and Epidermal Growth Factor-Receptor mRNAs in Dyshormonogenetic Goiters

Hipotireoidismo Congênito: Recentes Avanços em Genética Molecular

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