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Refinado por: assunto: Hipotireoidismo remover autor: Dias, V remover
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1
Molecular diagnosis of congenital hypothyroidism with total or partial iodide organification defect, screening for TPO mutations
Molecular diagnosis of congenital hypothyroidism with total or partial iodide organification defect, screening for TPO mutations
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Molecular diagnosis of congenital hypothyroidism with total or partial iodide organification defect, screening for TPO mutations

S. C. Neves I. G. S Rubio; Meyer Knobel; M. S Monteiro; V. L Pardo; A. L Galrão; V Dias; M Viana; A. J Chagas; GERALDO Medeiros-Neto; International Thyroid Congress (13. 2005 Buenos Aires, AR)

Thyroid New York v. 15, suppl. 1, p. S-228, res. P 524, 2005

New York American Thyroid Association 2005

Localização: FM - Fac. Medicina    (BCSEP 257 2005 )(Acessar)

2
Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect
Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect
Material Type:
Artigo 		Adicionar ao Meu Espaço

Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect

Solange Caires Neves Paola Rossi Mezalira; Vera M. A Dias; Antonio J Chagas; Maria Viana; Hector Targovnik; Meyer Knobel; Geraldo Medeiros-Neto; Ileana G. S Rubio

Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 54, n. 8, p. 732-737, 2010

São Paulo 2010

Localização: FM - Fac. Medicina    (BCSEP 343 2010 )(Acessar)

3
Five new cases of congenital goitrous hypothyroidism due to a P.R277X mutation in the thyroglobulin gene this mutation is the result of a mutational hot
Five new cases of congenital goitrous hypothyroidism due to a P.R277X mutation in the thyroglobulin gene this mutation is the result of a mutational hot
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Five new cases of congenital goitrous hypothyroidism due to a P.R277X mutation in the thyroglobulin gene this mutation is the result of a mutational hot

Viviane Pardo Ilena G. S Rubio; Meyer Knobel; M. S Monteiro; Carina Rivolta; Jussara Toniolo; Héctor Targovnik; Christian Moya; Vera Dias; Maria Viana; Antonio Chagas; GERALDO Medeiros-Neto; International Thyroid Congress (13. 2005 Buenos Aires, AR)

Thyroid New York v. 15, suppl. 1, p. S-230, res. P 531, 2005

New York American Thyroid Association 2005

Localização: FM - Fac. Medicina    (BCSEP 257 2005 )(Acessar)

4
Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant
Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant
Material Type:
Artigo 		Adicionar ao Meu Espaço

Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant

Denise Perone Geraldo Medeiros-Neto; Célia Regina Nogueira; Antonio José Chagas; Vera Maria Alves Dias; Maria Fátima Viana; Peter Kopp

Journal of pediatric endocrinology & metabolism London v. 29, n. 2, p. 193-201, 2016

London 2016

Localização: FM - Fac. Medicina    (BCSEP 122 2016 )(Acessar)

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Deste Autor:

  1. Chagas, A
  2. Dias, V
  3. Viana, M
  4. Medeiros-Neto, G
  5. Rubio, I

Neste Assunto:

  1. Hipotireoidismo
  2. Mutação Genética
  3. Resumos (Eventos)
  4. Monitorização Fetal
  5. Recém-Nascido

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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