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1
Methylation levels of sodium–iodide symporter (NIS) promoter in benign and malignant thyroid tumors with reduced NIS expression
Methylation levels of sodium–iodide symporter (NIS) promoter in benign and malignant thyroid tumors with reduced NIS expression
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Methylation levels of sodium–iodide symporter (NIS) promoter in benign and malignant thyroid tumors with reduced NIS expression

Galrão, A. L. ; Sodré, A. K. ; Camargo, R. Y. ; Friguglietti, C. U. ; Kulcsar, M. A. ; Lima, E. U. ; Medeiros-Neto, G. ; Rubio, I. G. S.

Endocrine, 2013-02, Vol.43 (1), p.225-229 [Periódico revisado por pares]

Boston: Springer US

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2
Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene
Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene
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Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene

MEDEIROS-NETO, G ; GIL-DA-COSTA, M. J ; SANTOS, C. L. S ; MEDINA, A. M ; COSTA E SILVA, J ; TSOU, R. M ; SOBRINHO-SIMOES, M

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.4162-4166 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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3
Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene
Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene
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Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene

KOPP, P ; ARSEVEN, O. K ; SABACAN, L ; KOTLAR, T ; DUPUIS, J ; CAVALIERE, H ; SANTOS, C. L. S ; JAMESON, J. L ; MEDEIROS-NETO, G

The journal of clinical endocrinology and metabolism, 1999, Vol.84 (1), p.336-341 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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4
A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit gene
A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit gene
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A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit gene

Medeiros-Neto, G ; Herodotou, D T ; Rajan, S ; Kommareddi, S ; de Lacerda, L ; Sandrini, R ; Boguszewski, M C ; Hollenberg, A N ; Radovick, S ; Wondisford, F E

The Journal of clinical investigation, 1996-03, Vol.97 (5), p.1250-1256 [Periódico revisado por pares]

United States

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5
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
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Clinical and molecular analysis of three Mexican families with Pendred's syndrome

GONZALEZ TREVINO, O ; KARAMANOGLU ARSEVEN, O ; CEBALLOS, C. J ; VIVES, V. I ; RAMIREZ, R. C ; GOMEZ, V. V ; MEDEIROS-NETO, G ; KOPP, P

European journal of endocrinology, 2001-06, Vol.144 (6), p.585-593 [Periódico revisado por pares]

Colchester: Portland Press

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6
Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres
Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres
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Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres

Silva, Marcia N. C. ; Rubió, Ileana G. S. ; Romão, Rossana ; Gebrin, Eloisa M. M. S. ; Buchpiguel, Carlos ; Tomimori, Eduardo ; Camargo, Rosalinda ; Cardia, Maria Silvia ; Medeiros-Neto, Geraldo

Clinical endocrinology (Oxford), 2004-03, Vol.60 (3), p.300-308 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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7
Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis
Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis
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Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis

MEDEIROS-NETO, G ; BUNDUKI, V ; TOMIMORI, E ; GOMES, S ; KNOBEL, M ; MARTIN, R. T ; ZUGAIB, M

The journal of clinical endocrinology and metabolism, 1997-12, Vol.82 (12), p.4239-4242 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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8
A novel mutation (Q40p) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia : Evidence for phenotypic variability in mother and child
A novel mutation (Q40p) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia : Evidence for phenotypic variability in mother and child
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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

CONGDON, Tamara ; NGUYEN, Lynda Q ; NOGUEIRA, Celia R ; HABIBY, Reema L ; MEDEIROS-NETO, Geraldo ; KOPP, Peter

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3962-3967 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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9
Prolonged follow-up of multinodular goitre patients treated with radioiodine preceded or not by human recombinant TSH
Prolonged follow-up of multinodular goitre patients treated with radioiodine preceded or not by human recombinant TSH
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Prolonged follow-up of multinodular goitre patients treated with radioiodine preceded or not by human recombinant TSH

Cardia, Maria Silvia ; Rubio, Ileana G S. ; Medeiros-Neto, Geraldo

Clinical endocrinology (Oxford), 2006-04, Vol.64 (4), p.474-474 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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10
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
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
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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

Gutnisky, Viviana J ; Moya, Christian M ; Rivolta, Carina M ; Domené, Sabina ; Varela, Viviana ; Toniolo, Jussara V ; Medeiros-Neto, Geraldo ; Targovnik, Héctor M

The journal of clinical endocrinology and metabolism, 2004-02, Vol.89 (2), p.646-657 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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