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1
Genotype-phenotype correlation in brazilian patients with congenital goiter and hypothyroidism due to thyroglobulin gene mutations
Genotype-phenotype correlation in brazilian patients with congenital goiter and hypothyroidism due to thyroglobulin gene mutations
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Genotype-phenotype correlation in brazilian patients with congenital goiter and hypothyroidism due to thyroglobulin gene mutations

V. Pardo I Knobel; J Toniolo; M Oliveira; P Kopp; Geraldo Antônio Medeiros Neto; Annual Meeting of the American Thyroid Association (79. 2008 Chicago, United States of America)

Thyroid New York v. 18, supl. 1, pag. S26, program 51, 2008

Chicago 2008

Localização: FM - Fac. Medicina    (BCSEP 168 2008 )(Acessar)

2
Naturally ocurring mutations in the thyroglobulin gene
Naturally ocurring mutations in the thyroglobulin gene
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Naturally ocurring mutations in the thyroglobulin gene

Jussara Vono-Toniolo Carina M Rivolta; Héctor M Targovnik; Geraldo Medeiros Neto Kopp. Peter

Thyroid New York v. 15, n. 2, p. 134-139, 2005

New York 2005

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

3
Naturally ocurring mutations in the thyroglobulin gene
Naturally ocurring mutations in the thyroglobulin gene
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Naturally ocurring mutations in the thyroglobulin gene

Jussara Vono-Toniolo Carina M Rivolta; Héctor M Targovnik; Geraldo Medeiros Neto Kopp. Peter

Thyroid New York v. 15, n. 2, p. 134-139, 2005

New York 2005

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

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

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

Thyroid New York v. 18, n. 7, p. 783-786, 2008

New York 2008

Localização: FM - Fac. Medicina    (BCSEP 168 2008 )(Acessar)

5
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

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

Thyroid New York v. 18, n. 7, p. 783-786, 2008

New York 2008

Localização: FM - Fac. Medicina    (BCSEP 168 2008 )(Acessar)

6
RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma [Carta]
RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma [Carta]
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RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma [Carta]

Rodrigo A. Toledo Rui M. B Maciel; Zoran Eric; Delmar M Lourenço Jr.; Janete M Cerutti; Charis Eng; Hartmut P Neumann; Sergio P Toledo

Thyroid New Rochelle v. 25, n. 8, p. 973-974, 2015

New Rochelle 2015

Acesso online. A biblioteca também possui exemplares impressos.

7
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)

8
Large fetal goiter in a patient with congenital hypothyroidism is associated with intron donor site mutation (G.IVS30+1G>T) of the thyroglobulin gene
Large fetal goiter in a patient with congenital hypothyroidism is associated with intron donor site mutation (G.IVS30+1G>T) of the thyroglobulin gene
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Large fetal goiter in a patient with congenital hypothyroidism is associated with intron donor site mutation (G.IVS30+1G>T) of the thyroglobulin gene

R. Possato I. G. S Rubio; M Knobel; M. H Oliveira; M Moura; C Rivolta; H. M Targovnik; G Medeiros-Neto; Annual Meeting on the American Thyroid Association (77. 2006 Phoenix)

Thyroid New York v. 16, n. 9, p. 906, res. 147, 2006

New York 2006

Localização: FM - Fac. Medicina    (BCSEP 352 2006 )(Acessar)

9
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)

10
Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect
Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect
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Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect

Antonio C. Nascimento Dulce R Guedes; Cecilia S Santos; Meyer Knobel; Ileana G. S Rubio; Geraldo Medeiros Neto

Thyroid New York v. 13, n. 9, p. 1145-1151, 2003

New York 2003

Localização: FM - Fac. Medicina    (BCSEP 2003 257 )(Acessar)

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Deste Autor:

  1. Medeiros-Neto, G
  2. Rubio, I
  3. Knobel, M
  4. Targovnik, H
  5. Pardo, V

Neste Assunto:

  1. Mutação Genética
  2. Hipotireoidismo
  3. Resumos (Eventos)
  4. Hipotireoidismo (Congênito)
  5. Doenças Hereditárias

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

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