skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: autor: Medeiros-Neto, G remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Methylation status of sodium-iodice symporter (NIS) promoter in thyroid cancer
Methylation status of sodium-iodice symporter (NIS) promoter in thyroid cancer
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Methylation status of sodium-iodice symporter (NIS) promoter in thyroid cancer

A L Galrão A K Sodre; R R Y Camargo; C U Friguglietti; M Kulcsar; E Urbano; M Knobel; Geraldo Antônio Medeiros Neto; I G S Rubio; Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP" (4. 2010 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina da USP" (4. 2010 São Paulo, SP)

Clinics São Paulo v. 65, supl.6, p. S63, res. 76, 2010

São Paulo 2010

Localização: FM - Fac. Medicina    (BCBIB 2010 ) e outros locais(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
Tireóide
Tireóide
Material Type:
Livro 		Adicionar ao Meu Espaço

Tireóide

Meyer Knobel Geraldo Antonio Medeiros-Neto

Lopes, Antonio Carlos (*), org. Tratado de Clínica Médica São Paulo : Roca, 2009

São Paulo Roca 2009

Localização: FM - Fac. Medicina    (WB115 T776 2ed. 2009 V.2 ) e outros locais(Acessar)

4
High Prevalence of Side Effects After Recombinant Human Thyrotropin–Stimulated Radioiodine Treatment with 30 mCi in Patients with Multinodular Goiter and Subclinical/Clinical Hyperthyroidism
High Prevalence of Side Effects After Recombinant Human Thyrotropin–Stimulated Radioiodine Treatment with 30 mCi in Patients with Multinodular Goiter and Subclinical/Clinical Hyperthyroidism
Material Type:
Artigo 		Adicionar ao Meu Espaço

High Prevalence of Side Effects After Recombinant Human Thyrotropin–Stimulated Radioiodine Treatment with 30 mCi in Patients with Multinodular Goiter and Subclinical/Clinical Hyperthyroidism

Rossana Romão Ileana G. S Rubio; Eduardo K Tomimori; Rosalinda Y Camargo; Meyer Knobel; Geraldo Medeiros-Neto

Thyroid New York v. 19, n. 9, p. 945-951, 2009

New York 2009

Localização: FM - Fac. Medicina    (BCSEP 207 2009 )(Acessar)

5
High Prevalence of Side Effects After Recombinant Human Thyrotropin–Stimulated Radioiodine Treatment with 30 mCi in Patients with Multinodular Goiter and Subclinical/Clinical Hyperthyroidism
High Prevalence of Side Effects After Recombinant Human Thyrotropin–Stimulated Radioiodine Treatment with 30 mCi in Patients with Multinodular Goiter and Subclinical/Clinical Hyperthyroidism
Material Type:
Artigo 		Adicionar ao Meu Espaço

High Prevalence of Side Effects After Recombinant Human Thyrotropin–Stimulated Radioiodine Treatment with 30 mCi in Patients with Multinodular Goiter and Subclinical/Clinical Hyperthyroidism

Rossana Romão Ileana G. S Rubio; Eduardo K Tomimori; Rosalinda Y Camargo; Meyer Knobel; Geraldo Medeiros-Neto

Thyroid New York v. 19, n. 9, p. 945-951, 2009

New York 2009

Localização: FM - Fac. Medicina    (BCSEP 207 2009 )(Acessar)

6
The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
Material Type:
Artigo 		Adicionar ao Meu Espaço

The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

Viviane Pardo Jussara Vono-Toniolo; Ileana G. S Rubio; Meyer Knobel; Roberta F Possato; Hector M Targovnik; Peter Kopp; Geraldo Medeiros-Neto

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 94, n. 8, p. 2938-2944, 2009

Philadelphia 2009

Acesso online. A biblioteca também possui exemplares impressos.

7
The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São Paulo
The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São Paulo
Material Type:
Artigo 		Adicionar ao Meu Espaço

The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São Paulo

Glaucia C. Duarte Eduardo K Tomimori; Rosalinda Y. A Camargo; Ileana G. S Rubio; Mauricio Wajngarten; Amanda G Rodrigues; Meyer Knobel; Geraldo A Medeiros-Neto

Clinics São Paulo v. 64, n. 2, p. 135-142, February, 2009

São Paulo 2009

Localização: FM - Fac. Medicina    (FM BCBIB )(Acessar)

8
The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São Paulo
The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São Paulo
Material Type:
Artigo 		Adicionar ao Meu Espaço

The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São Paulo

Glaucia C. Duarte Eduardo K Tomimori; Rosalinda Y. A Camargo; Ileana G. S Rubio; Mauricio Wajngarten; Amanda G Rodrigues; Meyer Knobel; Geraldo A Medeiros-Neto

Clinics São Paulo v. 64, n. 2, p. 135-142, February, 2009

São Paulo 2009

Localização: FM - Fac. Medicina    (FM BCBIB )(Acessar)

9
The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
Material Type:
Artigo 		Adicionar ao Meu Espaço

The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

Viviane Pardo Jussara Vono-Toniolo; Ileana G. S Rubio; Meyer Knobel; Roberta F Possato; Hector M Targovnik; Peter Kopp; Geraldo Medeiros-Neto

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 94, n. 8, p. 2938-2944, 2009

Philadelphia 2009

Acesso online. A biblioteca também possui exemplares impressos.

10
An outline concerning the potential use of recombinant human thyrotropin for improving radioiodine therapy of multinodular goiter
An outline concerning the potential use of recombinant human thyrotropin for improving radioiodine therapy of multinodular goiter
Material Type:
Artigo 		Adicionar ao Meu Espaço

An outline concerning the potential use of recombinant human thyrotropin for improving radioiodine therapy of multinodular goiter

Geraldo Medeiros-Neto Suemi Marui; Meyer Knobel

Endocrine Journal Tokyo v. 33, n. 2, p. 109-117, 2008

Tokyo 2008

Acesso online. A biblioteca também possui exemplares impressos.

Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (7)
  2. Disponível na Biblioteca (119)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (125)
  2. Livros  (20)
  3. Produções Acadêmicas  (2)
  4. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de1991  (8)
  2. 1991Até1994  (29)
  3. 1995Até1998  (18)
  4. 1999Até2003  (34)
  5. Após 2003  (58)
  6. Mais opções open sub menu

Idioma 

  1. Inglês  (87)
  2. Português  (65)
  3. Espanhol  (2)
  4. Mais opções open sub menu

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Medeiros-Neto, G
  2. Knobel, M
  3. Rubio, I
  4. Tomimori, E
  5. Camargo, R

Neste Assunto:

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

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

Buscando em bases de dados remotas. Favor aguardar.