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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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Lipid metabolism in subclinical hypothyroidism: plasma kinetics of triglyceride-rich lipoproteins and lipid transfers to high-density lipoprotein before and after levothyroxine treatment

Thyroid (New York, N.Y.), 2011-04, Vol.21 (4), p.347

2011

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Approach to and Treatment of Goiters

The Medical clinics of North America, 2012-03, Vol.96 (2), p.351-368

2012

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Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient

International journal of endocrinology, 2018-01, Vol.2018, p.4682876-10

2018

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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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Naturally Occurring Mutations in the Thyroglobulin Gene

Thyroid (New York, N.Y.), 2005-09, Vol.15 (9), p.121-1033

2005

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Recurrence of the p.R277X/p.R1511X compound heterozygous mutation in the thyroglobulin gene in unrelated families with congenital goiter and hypothyroidism: haplotype analysis using intragenic thyroglobulin polymorphisms

Journal of endocrinology, 2007-10, Vol.195 (1), p.167-177

2007

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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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Hypothyroidism in a Brazilian Kindred Due to Iodide Trapping Defect Caused by a Homozygous Mutation in the Sodium/Iodide Symporter Gene

Biochemical and biophysical research communications, 1997-11, Vol.240 (2), p.488-491

1997

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Thyrotropin Receptor Mutations in Hyperfunctioning Thyroid Adenomas from Brazil

Thyroid (New York, N.Y.), 1999-11, Vol.9 (11), p.163-1068

1999

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An Outline of Inherited Disorders of the Thyroid Hormone Generating System

Thyroid (New York, N.Y.), 2003-08, Vol.13 (8), p.771-801

2003

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Determination of thyroid volume by Sonography in healthy Brazilian schoolchildren

Journal of clinical ultrasound, 2002-05, Vol.30 (4), p.226-231

2002

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Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil

Clinical endocrinology (Oxford), 2000-07, Vol.53 (1), p.21-31

2000

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MiR-1 Is a Tumor Suppressor in Thyroid Carcinogenesis Targeting CCND2, CXCR4, and SDF-1α

The journal of clinical endocrinology and metabolism, 2011-09, Vol.96 (9), p.E1388-E1398

2011

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A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect

Clinical endocrinology (Oxford), 1999-08, Vol.51 (2), p.165-172

1999

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Relevance of iodine intake as a reputed predisposing factor for thyroid cancer

Arquivos brasileiros de endocrinologia e metabologia, 2007-07, Vol.51 (5), p.701-712

2007

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Levothyroxine Absorption in Morbidly Obese Patients Before and After Roux-En-Y Gastric Bypass (RYGB) Surgery

Obesity surgery, 2012-02, Vol.22 (2), p.253-258

2012

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Evaluation of a Coated-Tube Assay for Antithyrotropin Receptor Antibodies in Patients with Graves' Disease and Other Thyroid Disorders

Thyroid (New York, N.Y.), 2004-04, Vol.14 (4), p.295-300

2004

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A novel mutation (Q40p) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia : Evidence for phenotypic variability in mother and child

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3962-3967

2001

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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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Two Distinct Compound Heterozygous Constellations (R277X/IVS34–1G>C and R277X/R1511X) in the Thyroglobulin (TG) Gene in Affected Individuals of a Brazilian Kindred with Congenital Goiter and Defective TG Synthesis

The journal of clinical endocrinology and metabolism, 2004-02, Vol.89 (2), p.646-657

2004

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Excessive Iodine Intake and Ultrasonographic Thyroid Abnormalities in Schoolchildren

Journal of Pediatric Endocrinology and Metabolism, 2009, Vol.22 (4), p.327-334

2009

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Iodine Nutrition Improves in Latin America

Thyroid (New York, N.Y.), 2004-08, Vol.14 (8), p.59-599

2004

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

Lipid metabolism in subclinical hypothyroidism: plasma kinetics of triglyceride-rich lipoproteins and lipid transfers to high-density lipoprotein before and after levothyroxine treatment

Approach to and Treatment of Goiters

Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient

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

Naturally Occurring Mutations in the Thyroglobulin Gene

Recurrence of the p.R277X/p.R1511X compound heterozygous mutation in the thyroglobulin gene in unrelated families with congenital goiter and hypothyroidism: haplotype analysis using intragenic thyroglobulin polymorphisms

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

Hypothyroidism in a Brazilian Kindred Due to Iodide Trapping Defect Caused by a Homozygous Mutation in the Sodium/Iodide Symporter Gene

Thyrotropin Receptor Mutations in Hyperfunctioning Thyroid Adenomas from Brazil

An Outline of Inherited Disorders of the Thyroid Hormone Generating System

Determination of thyroid volume by Sonography in healthy Brazilian schoolchildren

Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil

MiR-1 Is a Tumor Suppressor in Thyroid Carcinogenesis Targeting CCND2, CXCR4, and SDF-1α

A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect

Relevance of iodine intake as a reputed predisposing factor for thyroid cancer

Levothyroxine Absorption in Morbidly Obese Patients Before and After Roux-En-Y Gastric Bypass (RYGB) Surgery

Evaluation of a Coated-Tube Assay for Antithyrotropin Receptor Antibodies in Patients with Graves' Disease and Other Thyroid Disorders

A novel mutation (Q40p) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia : Evidence for phenotypic variability in mother and child

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

Two Distinct Compound Heterozygous Constellations (R277X/IVS34–1G>C and R277X/R1511X) in the Thyroglobulin (TG) Gene in Affected Individuals of a Brazilian Kindred with Congenital Goiter and Defective TG Synthesis

Excessive Iodine Intake and Ultrasonographic Thyroid Abnormalities in Schoolchildren

Iodine Nutrition Improves in Latin America

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

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