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1
A Novel Mutation in CBX2 Gene in a Brazilian Patient with 46,XY Disorders of Sex Development (DSD) Due to Gonadal Dysgenesis
A Novel Mutation in CBX2 Gene in a Brazilian Patient with 46,XY Disorders of Sex Development (DSD) Due to Gonadal Dysgenesis
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A Novel Mutation in CBX2 Gene in a Brazilian Patient with 46,XY Disorders of Sex Development (DSD) Due to Gonadal Dysgenesis

C. R. Gomes S Domenice; B. B Mendonça; I. J. P Arnhold; E. M. F Costa; Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP) 2010 Costa do Sauípe, Bahia, Brazil) (21.

Hormone Research in Paediatrics Basel v. 74, n. suppl. 1, p. 6, res. 17, 2010

Basel 2010

Acesso online. A biblioteca também possui exemplares impressos.

2
Aconselhamento genético
Aconselhamento genético
Material Type:
Livro 		Adicionar ao Meu Espaço

Aconselhamento genético

Ivo Jorge Prado Arnhold Alexander Augusto de Lima Jorge

Mendonça, Berenice Bilharinho de; ed.; Arnhold, Ivo Jorge Prado (*). co.ed., Duarte, Alberto José da Silva; coord Investigação da baixa estatura : do fenótipo ao genótipo São Paulo : Atheneu, 2012

São Paulo Atheneu 2012

Localização: FM - Fac. Medicina    (WS330 I49 2012 )(Acessar)

3
Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty
Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty
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Artigo de Congresso 		Adicionar ao Meu Espaço

Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty

V. Brito B. B Mendonca Freitas, k.; I Arnhold; A. C Latronico; International Congress of Endocrinology (12. 2004 Lisboa)

Program and Abstracts Lisboa: International Society of Endocrinology, 2004

Lisboa International Society of Endocrinology 2004

Localização: FM - Fac. Medicina    (BCSEP 357 2004 )(Acessar)

4
Found in children with idiopathic short stature and NS-associated signs
Found in children with idiopathic short stature and NS-associated signs
Material Type:
Artigo 		Adicionar ao Meu Espaço

Found in children with idiopathic short stature and NS-associated signs

L. Ferreira L Montenegro; I Arnhold; Berenice Bilharinho de Mendonça; A Jorge; 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. 10, res. 26, 2007

Basel 2007

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

5
A novel mutation in the CXORF6 gene in patients with undertermined 46.XY disorders of sex development
A novel mutation in the CXORF6 gene in patients with undertermined 46.XY disorders of sex development
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A novel mutation in the CXORF6 gene in patients with undertermined 46.XY disorders of sex development

M. P. Brandão S Domenice; I. J. P Arnhold; E. M. F Costa; B. B Mendonça; International Congress of Endocrinology 2008 (13. Rio de Janeiro)

Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 52, supl. 6, parte II, p. S794, res. OP-098, 2008

São Paulo 2008

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

6
Estudo do gene da subunidade a, do receptor tipo a do àcido gama-amino butírico (GABRA1) em meninas com puberdade precoce dependente de gonadotrofinas idiopática
Estudo do gene da subunidade a, do receptor tipo a do àcido gama-amino butírico (GABRA1) em meninas com puberdade precoce dependente de gonadotrofinas idiopática
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Estudo do gene da subunidade a, do receptor tipo a do àcido gama-amino butírico (GABRA1) em meninas com puberdade precoce dependente de gonadotrofinas idiopática

Y. N. Brito Mendonça B. B.; K. C Freitas; I. J. P Arnhold; A. C Latronico; Congresso Brasileiro de Endocrinologia e Metabologia (26. 2004 Florianópolis)

Arquivos Brasileiros de Endocrinologia & Metabologia São Paulo v. 48, n. 5, supl. 1, p. S643, res. TLP 524, 2004

São Paulo Sociedade Brasileira de Endocrinologia e Metabologia - SBEM 2004

Item não circula. Consulte sua biblioteca.(Acessar)

7
Influence of GH receptor exon 3 polymorphism on the IGF-I response to variable GH doses during treatment of severe GH deficiency
Influence of GH receptor exon 3 polymorphism on the IGF-I response to variable GH doses during treatment of severe GH deficiency
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Artigo 		Adicionar ao Meu Espaço

Influence of GH receptor exon 3 polymorphism on the IGF-I response to variable GH doses during treatment of severe GH deficiency

Frederico Marchisotti Alexander Jorge; Luciana Montenegro; Karina Berger; Berenice Bilharinho de Mendonça; Ivo Arnhold; European society for paediatric endocrinology - ESPE (46. Helsinki, Finland 2007)

Hormone research Basel v. 68, suppl. 1, p. 139, res. P03-451, 2007

Basel 2007

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

8
The −202 A Allele of Insulin-Like Growth Factor Binding Protein-3 (IGFBP3) Promoter Polymorphism Is Associated with Higher IGFBP-3 Serum Levels and Better Growth Response to Growth Hormone Treatment in Patients with Severe Growth Hormone Deficiency
The −202 A Allele of Insulin-Like Growth Factor Binding Protein-3 (IGFBP3) Promoter Polymorphism Is Associated with Higher IGFBP-3 Serum Levels and Better Growth Response to Growth Hormone Treatment in Patients with Severe Growth Hormone Deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

The −202 A Allele of Insulin-Like Growth Factor Binding Protein-3 (IGFBP3) Promoter Polymorphism Is Associated with Higher IGFBP-3 Serum Levels and Better Growth Response to Growth Hormone Treatment in Patients with Severe Growth Hormone Deficiency

Everlayny Fiorot Costalonga Sonir R Antonini; Gil Guerra-Junior; Berenice Bilharinho Mendonca; Ivo J. P Arnhold; Alexander A. L Jorge

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 94, n. 2, p. 588-595, 2009

Philadelphia 2009

Acesso online. A biblioteca também possui exemplares impressos.

9
Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth
Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth
Material Type:
Artigo 		Adicionar ao Meu Espaço

Presence of several polyadenylation signal polymorphisms in IGF1 gene of children born small for gestational age (SGA) with and without postnatal catch-up growth

D. Coutinho R Coletta; E Costa; M Boguszewski; P Pachi; D Damiani; I Arnhold; Berenice Bilharinho de Mendonça; A Jorge; 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. 8, res. 22, 2007

Basel 2007

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

10
TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development
TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development
Material Type:
Artigo 		Adicionar ao Meu Espaço

TCF21 gene analysis in brazilian patients with 46,XY and 46,XX disorders of gonadal development

C. Gomes S Domenice; M Santos; I Arnhold; Berenice Bilharinho de Mendonça; E Costa; 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. 12, res. 33, 2007

Basel 2007

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

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Deste Autor:

  1. Arnhold, I
  2. Mendonça, B
  3. Jorge, A
  4. Costa, E
  5. Mendonca, B

Neste Assunto:

  1. Polimorfismo
  2. Mutação Genética
  3. Crianças
  4. Biologia Molecular
  5. Resumos (Eventos)

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

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