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1
Pituitary enlargement due to partial IGF-I insensitivity
Pituitary enlargement due to partial IGF-I insensitivity
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Pituitary enlargement due to partial IGF-I insensitivity

Soraya Milani Mariana Sarti de Paula; Lígia Batagin de Carvalho; Rodrigo José Custódio; Marcelo Amaral Ruiz; Ayrton Custódio Moreira; Sonir Roberto Rauber Antonini; Carlos Eduardo Martinelli Junior; Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) (50. 2011 Glasgow)

Hormone Research in Paediatrics Basel v.76, n. suppl.2, p. 302, res. PAO-141, 2011

Basel 2011

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2269582 estantes deslizantes ) e outros locais(Acessar)

2
Abnormal activation of the Wint/β-catenin pathway in childhood adrenocortical tumors (ACTs)
Abnormal activation of the Wint/β-catenin pathway in childhood adrenocortical tumors (ACTs)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Abnormal activation of the Wint/β-catenin pathway in childhood adrenocortical tumors (ACTs)

Letícia Ferro Leal Lívia Mara Mermejo; Leandra Naíra Zambelli Ramalho; Carlos Eduardo Martinelli Junior; Jose Andres Yunes; Ana Luiza Seidinger; Maria José Mastellaro; Silvia Regina Brandalise; Ayrton Custódio Moreira; Luiz Gonzaga Tone; Carlos Alberto Scrideli; Margaret de Castro; Sonir Roberto Rauber Antonini; Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) (50. 2011 Glasgow)

Hormone Research in Paediatrics Basel v.76, n. suppl.2, p. 33, res. FC-121, 2011

Basel 2011

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2269547 estantes deslizantes ) e outros locais(Acessar)

3
A homozygous NNT gene mutation identified by whole exoma sequencing (WES) in a boy with familial glucocorticoid deficiency (FGD) impairs mitochondrial oxidative stress
A homozygous NNT gene mutation identified by whole exoma sequencing (WES) in a boy with familial glucocorticoid deficiency (FGD) impairs mitochondrial oxidative stress
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

A homozygous NNT gene mutation identified by whole exoma sequencing (WES) in a boy with familial glucocorticoid deficiency (FGD) impairs mitochondrial oxidative stress

A. Bodoni F Coeli-Lacchini; L Sobral; Ayrton Custódio Moreira; Lucila Leico Kagohara Elias; Wilson Araújo da Silva Júnior; Andréia Machado Leopoldino; Margaret de Castro; Sonir Roberto Rauber Antonini; Congress of the Latin American Society of Pediatric Endocrinology (25. 2015 Puerto Varas)

Hormone Research in Paediatrics Basel v. 84, suppl. 2, p. 6, res. 001, 2015

Basel 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2740350 Estantes Deslizantes )(Acessar)

4
Underexpression of class II histocompatibility antigens (HLA) is related with poor prognosis in childhood adrenocortical tumors (ACT)
Underexpression of class II histocompatibility antigens (HLA) is related with poor prognosis in childhood adrenocortical tumors (ACT)
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Underexpression of class II histocompatibility antigens (HLA) is related with poor prognosis in childhood adrenocortical tumors (ACT)

Fabíola Leite Régia Caroline Peixoto Lira; Paola Fernanda Fedatto; Carlos Eduardo Martinelli Junior; Sonir Roberto Rauber Antonini; Rodrigo José Custódio; Margaret de Castro; Silvio Tucci Júnior; Luciano Neder Serafini; Leandra Naíra Zambelli Ramalho; Ana Seidinger; Izilda Cardinalli; Maria José Mastellaro; José A Yunes; Sílvia Brandalise; Luiz Gonzaga Tone; Carlos Alberto Scrideli; Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) (51. 2012 Leipzig)

Hormone Research in Paediatrics Basel v. 78, n. suppl. 1, p. 20-21, res. FC1-84, 2012

Basel 2012

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2347774 Estantes Deslizantes )(Acessar)

5
Analysis of DAX1 and SF1 genes and their interaction with genes involved in stem cell maintenance in adrenocortical tumors
Analysis of DAX1 and SF1 genes and their interaction with genes involved in stem cell maintenance in adrenocortical tumors
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Analysis of DAX1 and SF1 genes and their interaction with genes involved in stem cell maintenance in adrenocortical tumors

M. Cavalcanti L Leal; F Lacchini; Carlos Eduardo Martinelli Junior; Carlos Alberto Scrideli; Silvio Tucci Júnior; C Molina; J Yunes Mastellaro. M.; S Brandalise; I Cardinalli; Ayrton Custódio Moreira; Leandra Naíra Zambelli Ramalho; Margaret de Castro; Sonir Roberto Rauber Antonini; Congress of the Latin American Society of Pediatric Endocrinology (25. 2015 Puerto Varas)

Hormone Research in Paediatrics Basel v. 84, suppl. 2, p. 15, res. 020, 2015

Basel 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2740359 Estantes Deslizantes )(Acessar)

6
Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency
Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency

Aline F. Bodoni Fernanda Borchers Coeli-Lacchini; Juliana Lourenço Gebenlian; Lays Martin Sobral; Ayrton Custódio Moreira; Lucila Leico Kagohara Elias; Wilson Araújo da Silva Junior; Margaret de Castro; Andréia Machado Leopoldino; Sonir Roberto Rauber Antonini; Annual Meeting European Society for Paediatric Endocrinology - ESPE (58. 2019 Vienna)

Hormone Research in Paediatrics Basel v. 91, suppl. 1, p. 108, res. RFC13.4, 2019

Basel 2019

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3000316 Estantes Deslizantes )(Acessar)

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Deste Autor:

  1. Antonini, S
  2. Castro, M
  3. Moreira, A
  4. Martinelli Junior, C
  5. Ramalho, L

Neste Assunto:

  1. Mutação Genética
  2. Crianças
  3. Expressão Gênica
  4. Pediatria
  5. Glândula Pituitária

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

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