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Refinado por: autor: Arnhold, I remover assunto: Glândula Pituitária (Fisiopatologia) remover
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1
Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD)
Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Complete deletion of the PROP1 gene in two sibling with combined pituitary hormone deficiency (CPHD)

M. G. Abrao L Carvalho; M. V Leite; M Nishi; A Barbosa; I. J. P Arnhold; B. B Mendonça; Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP) (17. 2004 Angra dos Reis)

Journal of pediatric endocrinology and metabolism London v. 17, n. suppl.5, p. 1345, res. Poster 1, 2004

London 2004

Localização: FM - Fac. Medicina    (BCSEP 355 2004 ) e outros locais(Acessar)

2
High prevalence of adrenal insufficiency in adults with childhood onset growth hormone deficiency without PROP1 or HESX1 mutations
High prevalence of adrenal insufficiency in adults with childhood onset growth hormone deficiency without PROP1 or HESX1 mutations
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

High prevalence of adrenal insufficiency in adults with childhood onset growth hormone deficiency without PROP1 or HESX1 mutations

F. G. Marchisotti K Berger; L. R Carvalho; I. J. P Arnhold; B. B Mendonça; Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP) (17. 2004 Angra dos Reis)

Journal of pediatric endocrinology and metabolism London v. 17, n. suppl.5, p. 1343, res. Miniposter 10, 2004

London 2004

Localização: FM - Fac. Medicina    (BCSEP 355 2004 ) e outros locais(Acessar)

3
Hes1 as a possible digenic cause of hypopituitarism in two siblongs harboring a heterozygous c.301,302AG detection in Prop1
Hes1 as a possible digenic cause of hypopituitarism in two siblongs harboring a heterozygous c.301,302AG detection in Prop1
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Hes1 as a possible digenic cause of hypopituitarism in two siblongs harboring a heterozygous c.301,302AG detection in Prop1

A P Otto L Raetzman; M Y Nishi; I J P Arnhold; Berenice Bilharinho de Mendonça; L R Carvalho; Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP" (4. 2010 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina da USP" (4. 2010 São Paulo, SP)

Clinics São Paulo v. 65, supl.6, p. S72, res. 75, 2010

São Paulo 2010

Localização: FM - Fac. Medicina    (BCBIB 2010 ) e outros locais(Acessar)

4
Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant
Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant
Material Type:
Artigo 		Adicionar ao Meu Espaço

Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant

Frederico Guimarães Marchisotti Alexander Augusto Lima Jorge; Luciana Ribeiro Montenegro; Karina Berger; Luciani Renata Silveira de Carvalho; Berenice Bilharinho Mendonça; Ivo Jorge Prado Arnhold

Growth Hormone and IGF Research London v. 19, n. 2, p. 179-186, 2009

London 2009

Acesso online. A biblioteca também possui exemplares impressos.

5
Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant
Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant
Material Type:
Artigo 		Adicionar ao Meu Espaço

Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant

Frederico Guimarães Marchisotti Alexander Augusto Lima Jorge; Luciana Ribeiro Montenegro; Karina Berger; Luciani Renata Silveira de Carvalho; Berenice Bilharinho Mendonça; Ivo Jorge Prado Arnhold

Growth Hormone and IGF Research London v. 19, n. 2, p. 179-186, 2009

London 2009

Acesso online. A biblioteca também possui exemplares impressos.

6
Alta frequência de mutações no gene PROP1 em pacientes com hipopituitarismo
Alta frequência de mutações no gene PROP1 em pacientes com hipopituitarismo
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Alta frequência de mutações no gene PROP1 em pacientes com hipopituitarismo

Milena G Abrão Luciani Carvalho; Mirian Nishi; Maria G. F Osório; Ana Claudia Latronico; Suemi Marui; Vivian Stefan; Maristela V Leite; Berenice Bilharinho de Mendonça; Ivo J. P Arnhold; Congresso Paulista de Endocrinologia & Metabologia (5. 2003 São Paulo, SP)

Arquivos Brasileiros de Endocrinologia & Metabologia São Paulo v. 47, n. 2, supl. 2, p. S159, res. OR18, 2003

São Paulo 2003

Localização: FM - Fac. Medicina    (BCSEP 46 2008 )(Acessar)

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