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Refinado por: Biblioteca: FM - Fac. Medicina remover autor: Silveira, L remover
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1
A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty
A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty

Leticia F. G. Silveira Vinicius N Brito; Elaine M. F Costa; Ericka Trarbach; Milena G Teles; Berenice Bilharinho de Mendonça; Annual Meeting of the Endocrine Society's (88. 2006 Boston)

Program & Abstracts Boston, 2006

Boston 2006

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

2
A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty
A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty

L. G. Silveira M. A. G Santos; V. N Brito; E. M. F Costa; E Trarbach; M. G Teles; Berenice Bilharinho de Mendonça; A. C Latronico; Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP) (18. 2006 Viña del Mar, Chile)

Journal of pediatric endocrinology and metabolism London v. 19, n. suppl.3, p. 1067, res. 27, 2006

London 2006

Localização: FM - Fac. Medicina    (FM BCSEP 2006 199 )(Acessar)

3
A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty
A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty
Material Type:
Artigo 		Adicionar ao Meu Espaço

A novel missense mutation of KISS1 gene mutation in a boy with idiopathic gonadotropin-dependent precocious puberty

L. G. Silveira M. A. G Santos; V. N Brito; E. M. F Costa; E Trarbach; M. G Teles; Berenice Bilharinho de Mendonça; A. C Latronico; Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP) (18. 2006 Viña del Mar, Chile)

Journal of pediatric endocrinology and metabolism London v. 19, n. suppl.3, p. 1067, res. 27, 2006

London 2006

Localização: FM - Fac. Medicina    (FM BCSEP 2006 199 )(Acessar)

4
Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty
Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty

Leticia F. G. Silveira Cintia Tusset; Lucas Moura; Daiane Beneduzzi; Milena Teles; Alexander A. L Jorge; Ericka B Trarbach; Ana Claudia Latronico; 51th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) 51 2012 Leipzig, Germany

Hormone research in paediatrics Basel v.78, n. suppl. 1,res. P1-d3-378, p. 119, 2012

Basel 2012

Localização: FM - Fac. Medicina    (BCSEP 334 2012 ) e outros locais(Acessar)

5
Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency
Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

Ericka B. Trarbach Ana Paula Abreu; Leticia Ferreira Gontijo Silveira; Heraldo Mendes Garmes; Maria Tereza M Baptista; Milena Gurgel Teles; Elaine M. F Costa; Moosa Mohammadi; Nelly Pitteloud; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 95, n. 7, p. 3491-3496, 2010

Philadelphia 2010

Acesso online. A biblioteca também possui exemplares impressos.

6
Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency
Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

Ericka B. Trarbach Ana Paula Abreu; Leticia Ferreira Gontijo Silveira; Heraldo Mendes Garmes; Maria Tereza M Baptista; Milena Gurgel Teles; Elaine M. F Costa; Moosa Mohammadi; Nelly Pitteloud; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 95, n. 7, p. 3491-3496, 2010

Philadelphia 2010

Acesso online. A biblioteca também possui exemplares impressos.

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