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Refinado por: autor: Mendonça, B remover Almeida, M remover
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1
Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction
Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction
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Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction

M. Queiroz Almeida M Gerdulo; A. Lima Augusto Jorge; M. Yumie Nishi; A Lerario; M. Barrison Villares Fragoso; Berenice Bilharinho de Mendonça; Ana Claudia Latronico Xavier; Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP (19. Mar del Plata, Argentina 2007)

Hormone research Basel v. 68, suppl. 4, p. 24, res. 64, 2007

Basel 2007

Localização: FM - Fac. Medicina    (BCSEP 161 2007 )(Acessar)

2
Genetics of primary macronodular adrenal hyperplasia
Genetics of primary macronodular adrenal hyperplasia
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Genetics of primary macronodular adrenal hyperplasia

Maria Candida Barisson Villares Fragoso Guilherme Asmar Alencar; Antonio Marcondes Lerario; Isabelle Bordeaux; Madson Queiroz Almeida; Berenice B Mendonça; Andre Lacroix

Journal of Endocrinology Bristol v. 224, n. 1, p. R31-R43, 2015

Bristol 2015

Acesso online. A biblioteca também possui exemplares impressos.

3
ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia
ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia
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ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia

Guilherme Asmar Alencar Antonio Marcondes Lerario; Mirian Yumie Nishi; Beatriz Marinho de Paula Mariani; Madson Queiroz Almeida; Johanne Tremblay; Pavel Hamet; Maria Claudis Nogueira Zerbini; Gilberto Carlos Gomes; Isabelle Bordeau; Maria Adelaide Albergaria Pereira; Manoel de Souza Rocha; Jose Carlos Chambo; Andre Lacroix; Berenice Bilharinho Mendonça; Maria Candida B. Villares Fragoso

Journal of Clinical Endocrinology and Metabolism Springfield v. 99, n. 8, p. E1501-E1509, 2014

Springfield 2014

Localização: FM - Fac. Medicina    (BCSEP 023 2014 )(Acessar)

4
The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH)
The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH)
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The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH)

Isadora Pontes Cavalcante Mirian Yumie Nishi; Maria Claudia Nogueira Zerbini; Madson Queiroz de Almeida; Vânia Balderrama Brondani; Maria Luiza Anhaia de Arruda Botelho; Fabio Yoshiaki Tanno; Victor Srougi; José Luis Chambo; Berenice Bilharinho de Mendonça; Jérôme Bertherat; Claudimara Ferini Pacicco Lotfi; Maria Candida B Fragoso

Molecular and cellular endocrinology v. 460, n. C, p. 36-46, 2018

Shannon 2018

Localização: FM - Fac. Medicina    (OPI 25684 2018 )(Acessar)

5
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole
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Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole

Madson Queiroz Almeida Vinicius Nahime Brito; Thereza Selma S Lins; Gil Guerra-Júnior; Margaret de Castro; Sonir Roberto Antonini; Ivo Jorge Prado Arnhold; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Clinical Endocrinology Oxford v. 69, n. 1, p. 93-98, 2008

Oxford 2008

Localização: FM - Fac. Medicina    (BCSEP 227 2008 ) e outros locais(Acessar)

6
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole
Material Type:
Artigo 		Adicionar ao Meu Espaço

Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole

Madson Queiroz Almeida Vinicius Nahime Brito; Thereza Selma S Lins; Gil Guerra-Júnior; Margaret de Castro; Sonir Roberto Antonini; Ivo Jorge Prado Arnhold; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Clinical Endocrinology Oxford v. 69, n. 1, p. 93-98, 2008

Oxford 2008

Localização: FM - Fac. Medicina    (BCSEP 227 2008 ) e outros locais(Acessar)

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Deste Autor:

  1. Mendonça, B
  2. Almeida, M
  3. Fragoso, M
  4. Lerario, A
  5. Nishi, M

Neste Assunto:

  1. Mutação Genética
  2. Endocrinologia
  3. Puberdade Precoce
  4. Expressão Gênica
  5. Cultura De Células

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

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