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Refinado por: autor: Mendonça, B remover Nome da Publicação: Hormone Research in Paediatrics remover
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1
Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE)
Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE)

M. França A Jorge; L Carvalho; A Otto; F Corrêa; E Costalonga Mendonça. B.; I Arnhold; Annual Meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP) (22. 2011 Cartagena de Indias, Colombia)

Hormone Research in Paediatrics Basel v. 76, n. suppl. 4, p. 1, res. 2, 2011

Basel 2011

Acesso online

2
Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients
Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients

Andria C. V. Lido Marcela M França; Aline P Otto; Luciani R Carvalho; Berenice Bilharinho de Mendonça; Ivo J.P Arnhold; Alexander Augusto de Lima Jorge; European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting (9. 2013 Milan, Italy)

Hormone Research in Paediatrics Basel v. 80, suppl. 1, p. 295, res. P2-d1-952, 2013

Basel 2013

Localização: FM - Fac. Medicina    (BCSEP 418 2013 )(Acessar)

3
Copy number variants in Brazilian patients with congenital hypopituirarism
Copy number variants in Brazilian patients with congenital hypopituirarism
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Copy number variants in Brazilian patients with congenital hypopituirarism

Fernanda A. Correa Marcela M Franca; Ana P. M Canton; Aline p Otto; Everlayne F Costalonga; Vinicius N Brito; Luciani R Carvalho; Silvia Costa; Ivo J. P Arnhold; Alexander Augusto de Lima Jorge; Carla Rosenberg; Berenice Bilharinho de Mendonça; European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting (9. 2013 Milan, Italy)

Hormone Research in Paediatrics Basel v. 80, suppl. 1, p. 161, res. P1-d1-506, 2013

Basel 2013

Localização: FM - Fac. Medicina    (BCSEP 418 2013 )(Acessar)

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Deste Autor:

  1. Carvalho, L
  2. Mendonça, B
  3. Arnhold, I
  4. Jorge, A
  5. Otto, A

Neste Assunto:

  1. Endocrinopatias
  2. Hormônio Do Crescimento (Deficiência)
  3. Resumos (Eventos)
  4. Fenótipos
  5. Genes (Análise)

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

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