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Refinado por: assunto: Thyroglobulin - Blood remover assunto: Thyrotropin - Blood remover
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1
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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5
High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis
High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis
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High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis

Avbelj, Magdalena ; Tahirovic, Husref ; Debeljak, Marusa ; Kusekova, Maria ; Toromanovic, Alma ; Krzisnik, Ciril ; Battelino, Tadej

European journal of endocrinology, 2007-05, Vol.156 (5), p.511-519 [Periódico revisado por pares]

Colchester: European Society of Endocrinology

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6
The Site of the Molecular Defect in the Thyroid Gland of the hyt/hyt Mouse: Abnormalities in the TSH Receptor-G Protein Complex
The Site of the Molecular Defect in the Thyroid Gland of the hyt/hyt Mouse: Abnormalities in the TSH Receptor-G Protein Complex
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The Site of the Molecular Defect in the Thyroid Gland of the hyt/hyt Mouse: Abnormalities in the TSH Receptor-G Protein Complex

Stein, S A ; Zakarija, M ; McKenzie, J M ; Shanklin, D R ; Palnitkar, M B ; Adams, P M

Thyroid (New York, N.Y.), 1991, Vol.1 (3), p.257-266 [Periódico revisado por pares]

United States

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7
Safe Range of Iodine Intake Levels: A Comparative Study of Thyroid Diseases in Three Women Population Cohorts with Slightly Different Iodine Intake Levels
Safe Range of Iodine Intake Levels: A Comparative Study of Thyroid Diseases in Three Women Population Cohorts with Slightly Different Iodine Intake Levels
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Safe Range of Iodine Intake Levels: A Comparative Study of Thyroid Diseases in Three Women Population Cohorts with Slightly Different Iodine Intake Levels

Teng, Xiaochun ; Shi, Xiaoguang ; Shan, Zhongyan ; Jin, Ying ; Guan, Haixia ; Li, Yushu ; Yang, Fan ; Wang, Weibo ; Tong, Yajie ; Teng, Weiping

Biological trace element research, 2008, Vol.121 (1), p.23-30 [Periódico revisado por pares]

New York: Humana Press Inc

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8
Suppressive Therapy with Levothyroxine for Euthyroid Diffuse and Nodular Goiter
Suppressive Therapy with Levothyroxine for Euthyroid Diffuse and Nodular Goiter
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Suppressive Therapy with Levothyroxine for Euthyroid Diffuse and Nodular Goiter

GÜLLÜ, SEVIM ; GÜRSES, M. ALI ; BASKAL, NILGÜN ; UYSAL, A. RIZA ; KAMEL, A. NURI ; ERDOGAN, GÜRBÜZ

Endocrine Journal, 1999, Vol.46(1), pp.221-226 [Periódico revisado por pares]

Japan: The Japan Endocrine Society

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9
Clinical and laboratory features of children and adolescents with congenital hypothyroidism due to dyshormonogenesis in southern Brazil
Clinical and laboratory features of children and adolescents with congenital hypothyroidism due to dyshormonogenesis in southern Brazil
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Clinical and laboratory features of children and adolescents with congenital hypothyroidism due to dyshormonogenesis in southern Brazil

Ramos, Juliana Cristina Romero Rojas ; Lacerda Filho, Luiz de ; DeMartini, Adriane de André Cardoso ; Silveira, Rodrigo Bruel da ; Pereira, Rosana Marques ; Sandrini Neto, Romolo ; França, Suzana Nesi

Arquivos brasileiros de endocrinologia e metabologia, 2012-04, Vol.56 (3), p.201-208

Brazil: Sociedade Brasileira de Endocrinologia e Metabologia

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10
Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism
Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism
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Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism

AMBRUGGER, Petra ; STOEVA, Iva ; BIEBERMANN, Heike ; TORRESANI, Toni ; LEITNER, Christa ; GRATERS, Annette

European journal of endocrinology, 2001-07, Vol.145 (1), p.19-24 [Periódico revisado por pares]

Colchester: Portland Press

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