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The Journal of Clinical Endocrinology and Metabolism|February 7, 2004
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 synthesisViviana J Gutnisky, Christian M Moya, Carina M Rivolta, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|March 12, 2005
[Echographic evaluation of the thyroid gland and urinary iodine concentration in school children from various regions of the State of São Paulo, Brazil]Glaucia C Duarte, Eduardo K Tomimori, Rosângela A Boriolli, et al.
The Journal of Endocrinology|October 4, 2007
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 polymorphismsMariela Caputo, Carina M Rivolta, Viviana J Gutnisky, et al.
Clinics (Sao Paulo, Brazil)|February 17, 2009
The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São PauloGlaucia C Duarte, Eduardo K Tomimori, Rosalinda Y A Camargo, et al.
Endocrine Pathology|April 1, 1997
Clinical, Pathological, and Molecular Studies of Two Families with Iodide Organification DefectKatia G. M. Rego, Ana Elisa C. Billerbeck, Hector M. Targovnik, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defectSolange Caires Neves, Paola Rossi Mezalira, Vera M A Dias, et al.
The Journal of Clinical Endocrinology and Metabolism|January 18, 2014
Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) enhancer (NDE) is associated with reduced NIS expression in thyroid tumorsAna Luiza Galrão, Rosalinda Y Camargo, Celso U Friguglietti, et al.
Clinical Endocrinology|March 11, 2004
Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitresMarcia N C Silva, Ileana G S Rubió, Rossana Romão, et al.
Thyroid : Official Journal of the American Thyroid Association|July 18, 2008
Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutationsViviane Pardo, Ileana G S Rubio, Meyer Knobel, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutationIleana G S Rubio, Ana Luiza Galrao, Viviane Pardo, et al.
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