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Refinado por: assunto: Thyroglobulin - Blood remover assunto: Thyrotropin - Blood remover
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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
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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2
Prognostic value of serial serum thyroglobulin determinations after total thyroidectomy for differentiated thyroid cancer
Prognostic value of serial serum thyroglobulin determinations after total thyroidectomy for differentiated thyroid cancer
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Prognostic value of serial serum thyroglobulin determinations after total thyroidectomy for differentiated thyroid cancer

LIMA, N ; CAVALIERE, H ; TOMIMORI, E ; KNOBEL, M ; MEDEIROS-NETO, G

Journal of endocrinological investigation, 2002-02, Vol.25 (2), p.110-115 [Periódico revisado por pares]

Milano: Kurtis

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3
Elevated Anti-Galactosyl Antibody Titers in Endemic Goiter
Elevated Anti-Galactosyl Antibody Titers in Endemic Goiter
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Elevated Anti-Galactosyl Antibody Titers in Endemic Goiter

Knobel, M ; Umezawa, E S ; Cardia, M S ; Martins, M J ; Correa, M L ; Gianella-Neto, D ; Caulier, C ; Medeiros-Neto, G

Thyroid (New York, N.Y.), 1999-05, Vol.9 (5), p.493-498 [Periódico revisado por pares]

United States

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4
Phenotypic Variation Among Four Family Members with Congenital Hypothyroidism Caused by Two Distinct Thyroglobulin Gene Mutations
Phenotypic Variation Among Four Family Members with Congenital Hypothyroidism Caused by Two Distinct Thyroglobulin Gene Mutations
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Phenotypic Variation Among Four Family Members with Congenital Hypothyroidism Caused by Two Distinct Thyroglobulin Gene Mutations

Pardo, Viviane ; Rubio, Ileana G.S. ; Knobel, Meyer ; Aguiar-Oliveira, Manoel H. ; Santos, Marcos M. ; Gomes, Simone A. ; Oliveira, Carla R.P. ; Targovnik, Hector M. ; Medeiros-Neto, Geraldo

Thyroid (New York, N.Y.), 2008-07, Vol.18 (7), p.783-786 [Periódico revisado por pares]

United States: Mary Ann Liebert, Inc

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