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1
Two novel nonsense mutations of the fibroblast growth factor 8 in patients with congenital isolated hypogonadotropic hypogonadism
Two novel nonsense mutations of the fibroblast growth factor 8 in patients with congenital isolated hypogonadotropic hypogonadism
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Two novel nonsense mutations of the fibroblast growth factor 8 in patients with congenital isolated hypogonadotropic hypogonadism

E. B. Trarbach A. P Abreu; E. M. F Costa; M Teles; G Guerra Júnior; M. T. M Baptista; H. M Garmes; Margaret de Castro; 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 1683161 ) e outros locais(Acessar)

2
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)

3
A novel splice site mutation in GPR54 in 2 siblings with normosmic isolated hypogonadotrophic hypogonadism
A novel splice site mutation in GPR54 in 2 siblings with normosmic isolated hypogonadotrophic hypogonadism
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A novel splice site mutation in GPR54 in 2 siblings with normosmic isolated hypogonadotrophic hypogonadism

M. G. Teles A Mukherjee; E. B Trarbach; G Guerra Junior; E. M. F Costa; M. T. M Batista; M Castro; Berenice Bilharinho de Mendonça; U. B Kaiser; A. C Latronico; 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. S84, res. 398, 2007

São Paulo 2007

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

4
Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism
Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism

Beatriz R. Versiani Ericka Trarbach; Marcel Koenigkam-Santos; Antonio Carlos dos Santos; Lucila Leico Kagohara Elias; Ayrton Custódio Moreira; Ana Claudia Latronico; Margaret de Castro

Clinical Endocrinology Oxford v. 66, p. 173-179, 2007

Oxford 2007

Localização: FM - Fac. Medicina    (BCSEP 001 2007 ) e outros locais(Acessar)

5
Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism
Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism

Beatriz R. Versiani Ericka Trarbach; Marcel Koenigkam-Santos; Antonio Carlos dos Santos; Lucila Leico Kagohara Elias; Ayrton Custódio Moreira; Ana Claudia Latronico; Margaret de Castro

Clinical Endocrinology Oxford v. 66, p. 173-179, 2007

Oxford 2007

Localização: FM - Fac. Medicina    (BCSEP 001 2007 ) e outros locais(Acessar)

6
Novel FGF8 gene mutations in patients with congenital isolated isolated hypogonadotropic hypogonadism
Novel FGF8 gene mutations in patients with congenital isolated isolated hypogonadotropic hypogonadism
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Novel FGF8 gene mutations in patients with congenital isolated isolated hypogonadotropic hypogonadism

E. B. Trarbach M. G Teles; E. M. F Costa; A. P Abreu; B. B Mendonça; M Castro; G Guerra; H. M Garmes; M. T. M Baptista; Ana Claudia X Latronico; International Congress of Endocrinology 2008 (13. Rio de Janeiro)

Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 52, supl. 6, parte II, p. S793, res. OP-095, 2008

São Paulo 2008

Localização: FM - Fac. Medicina    (BCSEP 382 2008 )(Acessar)

7
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification detection of a hemizygosis for the fibroblast growth factor receptor 1
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification detection of a hemizygosis for the fibroblast growth factor receptor 1
Material Type:
Artigo 		Adicionar ao Meu Espaço

Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification detection of a hemizygosis for the fibroblast growth factor receptor 1

Ericka Barbosa Trarbach Milena Gurgel Teles; Elaine Maria Frade Costa; Ana Paula Abreu; Heraldo Mendes Garmes; Gil Guerra Junior; Maria Tereza Matias Baptista; Margaret de Castro; Berenice Bilharinho Mendonca; Ana Claudia Latronico

Clinical endocrinology Oxford v. 72, n. 3, p. 371-376, 2010

Oxford 2010

Acesso online. A biblioteca também possui exemplares impressos.

8
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification detection of a hemizygosis for the fibroblast growth factor receptor 1
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification detection of a hemizygosis for the fibroblast growth factor receptor 1
Material Type:
Artigo 		Adicionar ao Meu Espaço

Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification detection of a hemizygosis for the fibroblast growth factor receptor 1

Ericka Barbosa Trarbach Milena Gurgel Teles; Elaine Maria Frade Costa; Ana Paula Abreu; Heraldo Mendes Garmes; Gil Guerra Junior; Maria Tereza Matias Baptista; Margaret de Castro; Berenice Bilharinho Mendonca; Ana Claudia Latronico

Clinical endocrinology Oxford v. 72, n. 3, p. 371-376, 2010

Oxford 2010

Acesso online. A biblioteca também possui exemplares impressos.

9
TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood
TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood
Material Type:
Artigo 		Adicionar ao Meu Espaço

TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

Elena Gianetti Cintia Tusset; Sekoni D Noel; Margaret G Au; Andrew A Dwyer; Virginia A Hughes; Ana Paula Abreu; Jessica Carroll; Ericka Trarbach; Leticia F. G Silveira; Elaine M. F Costa; Berenice Bilharinho de Mendonça; Margaret de Castro; Adriana Lofrano; Janet E Hall; Erol Bolu; Metin Ozata; Richard Quinton; John K Amory; Susan E Stewart; Wiebke Arlt; Trevor R Cole; William F Crowley; Ursula B Kaiser; Ana Claudia Latronico; Stephanie B Seminara

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 95, n. 5, p. 2857-2867, 2010

Philadelphia 2010

Acesso online. A biblioteca também possui exemplares impressos.

10
TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood
TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood
Material Type:
Artigo 		Adicionar ao Meu Espaço

TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

Elena Gianetti Cintia Tusset; Sekoni D Noel; Margaret G Au; Andrew A Dwyer; Virginia A Hughes; Ana Paula Abreu; Jessica Carroll; Ericka Trarbach; Leticia F. G Silveira; Elaine M. F Costa; Berenice Bilharinho de Mendonça; Margaret de Castro; Adriana Lofrano; Janet E Hall; Erol Bolu; Metin Ozata; Richard Quinton; John K Amory; Susan E Stewart; Wiebke Arlt; Trevor R Cole; William F Crowley; Ursula B Kaiser; Ana Claudia Latronico; Stephanie B Seminara

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 95, n. 5, p. 2857-2867, 2010

Philadelphia 2010

Acesso online. A biblioteca também possui exemplares impressos.

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Deste Autor:

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

Neste Assunto:

  1. Hipogonadismo
  2. Mutação Genética
  3. Fibroblastos
  4. Testosterona
  5. Fenótipos

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

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