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1
Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2
Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2

A. P. Abreu E. B Trarbach; Margaret de Castro; E. M. F Costa; B Versiani; G Guerra Júnior; M. T. M Baptista; H. M Garmes; Berenice Bilharinho de Mendonça; A. C Latronico; Annual Meeting of the Endocrine Society (90. 2008 San Francisco)

Program and Abstracts Book San Francisco, 2008

San Francisco 2008

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1682900 ) e outros locais(Acessar)

2
A homozygous nonsense mutation in the prokineticin receptor-2 gene in a patient with sporadic kallmann syndrome
A homozygous nonsense mutation in the prokineticin receptor-2 gene in a patient with sporadic kallmann syndrome
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A homozygous nonsense mutation in the prokineticin receptor-2 gene in a patient with sporadic kallmann syndrome

A. P. Abreu E. B Trarbach; M Castro; E. M. F Costa; B Versiani; M. T. M Baptista; H. M Garnes; Berenice Bilharinho de Mendonça; A. C Latronico; T. A. S. S Bachega; Simpósio avanços em pesquisas médicas (3. 2007 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina - USP" (3. 2007 São Paulo, SP)

Clinics São Paulo v. 62, supl. 3, p. S82, res. 276, 2007

São Paulo 2007

Localização: FM - Fac. Medicina    (BCBIB ) e outros locais(Acessar)

3
Novas mutações no gene do receptor tipo 2 da proquineticina em pacientes com síndrome de Kallmann
Novas mutações no gene do receptor tipo 2 da proquineticina em pacientes com síndrome de Kallmann
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Novas mutações no gene do receptor tipo 2 da proquineticina em pacientes com síndrome de Kallmann

A. P. S. Abreu E. B Trarbach; M Castro; E. M. F Costa; B. R Versiani; M. T. M Baptista; H. M Garmes; B. B Mendonça; A. C Latronico; Congresso Paulista de Endocrinologia e Metabolismo (7. 2007 São Paulo)

Arquivos Brasileiros de Endocrinologia & Metabologia São Paulo v. 51, n. 3, supl. 1, p. S112, 04.004, 2007

São Paulo Sociedade Brasileira de Endocrinologia e Metabologia - SBEM 2007

Localização: FM - Fac. Medicina    (BCSEP 430 2007 )(Acessar)

4
Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome
Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome

Ana Paula Abreu Ericka Trarbach; Margaret de Castro; Elaine M. F Costa; Beatriz Versiani; Maria Tereza M Baptista; Heraldo M Garmes; Berenice B Mendonça; Ana Claudia Latronico; The Endocrine Society's Annual Meeting (ENDO) (89. 2007 Toronto)

Program and Abstracts Toronto, 2007

Toronto 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1619599 ) e outros locais(Acessar)

5
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome

Ana Paula Abreu Ericka Barbosa Trarbach; Margaret de Castro; Elaine Maria Frade Costa; Beatriz Versiani; Maria Tereza Matias Baptista; Heraldo Mendes Garmes; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 93, n. 10, p. 4113-4118, 2008

Philadelphia 2008

Localização: FM - Fac. Medicina    (BCSEP 230 2008 ) e outros locais(Acessar)

6
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome

Ana Paula Abreu Ericka Barbosa Trarbach; Margaret de Castro; Elaine Maria Frade Costa; Beatriz Versiani; Maria Tereza Matias Baptista; Heraldo Mendes Garmes; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 93, n. 10, p. 4113-4118, 2008

Philadelphia 2008

Localização: FM - Fac. Medicina    (BCSEP 230 2008 ) e outros locais(Acessar)

7
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome

Luciana Ribeiro Montenegro Leticia F. G Silveira; Cintia Tusset; Margaret de Castro; Beatriz R Versiani; Ana Claudia Latronico; Berenice Bilharinho Mendonca; Ericka B Trarbach

Fertility and Sterility New York v.100, n.3, p. 854-859, 2013

New York 2013

Localização: FM - Fac. Medicina    (BCSEP 167 2013 ) e outros locais(Acessar)

8
Novel FGFR1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia
Novel FGFR1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Novel FGFR1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia

Ericka B. Trarbach Elaine M. F Costa; Beatriz R Versiani; Margaret Castro; Maria T. M Baptista; Heraldo M Garmes; Berenice B Mendonça; Ana Claudia Latronico; Annual Meeting of the Endocrine Society (88. 2006 Massachusetts)

Program & Abstracts Massachusetts, 2006

Massachusetts 2006

Localização: FM - Fac. Medicina    (FM BCSEP 245 2006 ) e outros locais(Acessar)

9
Novel fibroblast growtj factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia
Novel fibroblast growtj factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel fibroblast growtj factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia

Ericka Barbosa Trarbach Elaine Maria Frade Costa; Beatriz Versiani; Margaret de Castro; Maria Tereza Matias Baptista; Heraldo Mendes Garmes; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 91, n. 10, p. 4006-4012, 2006

Philadelphia 2006

Localização: FM - Fac. Medicina    (FM BCSEP 103 2006 )(Acessar)

10
Novel fibroblast growtj factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia
Novel fibroblast growtj factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel fibroblast growtj factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia

Ericka Barbosa Trarbach Elaine Maria Frade Costa; Beatriz Versiani; Margaret de Castro; Maria Tereza Matias Baptista; Heraldo Mendes Garmes; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 91, n. 10, p. 4006-4012, 2006

Philadelphia 2006

Localização: FM - Fac. Medicina    (FM BCSEP 103 2006 )(Acessar)

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Deste Autor:

  1. Latronico, A
  2. Trarbach, E
  3. Castro, M
  4. Versiani, B
  5. Costa, E

Neste Assunto:

  1. Endocrinologia
  2. Síndrome De Kallmann
  3. Mutação Genética
  4. Hipogonadismo
  5. Fatores De Crescimento

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

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