skip to main content
Idioma:
Só é possível identificar-se se os cookies estiverem habilitados.
Refinado por: Nome da Publicação: Hormone Research in Paediatrics remover
Result Number Material Type Add to My Shelf Action Record Details and Options
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
Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit
Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit
Material Type:
Artigo 		Adicionar ao Meu Espaço

Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit

Débora Macedo Cabral Sonir Roberto Rauber Antonini; Rodrigo José Custódio; Carlos Eduardo Martinelli Junior; Carlos Antonio Bruno da Silva

Hormone Research in Paediatrics Basel v. 79, n. 6, p. 373-378, 2013

Basel 2013

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2429210 Estantes Deslizantes )(Acessar)

4
Time course of central precocious puberty development caused by an MKRN3 gene mutation a prismatic care
Time course of central precocious puberty development caused by an MKRN3 gene mutation a prismatic care
Material Type:
Artigo 		Adicionar ao Meu Espaço

Time course of central precocious puberty development caused by an MKRN3 gene mutation a prismatic care

Monica F. Stecchini Delanie B Macedo; Ana Claudia S Reis; Ana Paula Abreu; Ayrton Custódio Moreira; Margaret de Castro; Ursula B Kaiser; Ana Claudia Latronico; Sonir Roberto Rauber Antonini

Hormone Research in Paediatrics Basel v. 86, n. 2, p. 126-130, 2016

Basel 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2853580 Estantes Deslizantes )(Acessar)

5
Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during central precocious puberty therapy
Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during central precocious puberty therapy
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during central precocious puberty therapy

Mariana Sarti de Paula Rafaela Ricco; Rodrigo Custodio; Soraya Sader Milani; Patricia Atique; Ayrton Custódio Moreira; Sonir Roberto Rauber Antonini; Raphael Del Roio Liberatore Junior; Carlos Eduardo Martinelli Junior; Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) (54. 2015 Barcelona)

Hormone Research in Paediatrics Basel v. 84, suppl. 1, p. 236-237, res. P2-400, 2015

Basel 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2740246 Estantes Deslizantes )(Acessar)

6
Adult height in 299 patients with Turner syndrome with or without growth hormone therapy results and literature review
Adult height in 299 patients with Turner syndrome with or without growth hormone therapy results and literature review
Material Type:
Artigo 		Adicionar ao Meu Espaço

Adult height in 299 patients with Turner syndrome with or without growth hormone therapy results and literature review

Naiara Castelo Branco Dantas Adriana F Braz; Alexsandra Malaquias; Sofia Lemos-Marini; Ivo Jorge Prado Arnhold; Ester Silveira Ramos; Sonir Roberto Rauber Antonini; Gil Guerra-Junior; Berenice Bilharinho de Mendonça; Alexander Augusto de Lima Jorge; Renata C Scalco

Hormone Research in Paediatrics Basel v. 94, n. 1-2, p. 63-70, 2021

Basel 2021

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3049226 Acervo Digital )(Acessar)

7
Histopathological criteria for paediatric adrenocortical carcinoma
Histopathological criteria for paediatric adrenocortical carcinoma
Material Type:
Artigo 		Adicionar ao Meu Espaço

Histopathological criteria for paediatric adrenocortical carcinoma

Victor Pereira Paschoalin Silvio Tucci Júnior; Andrey Garcia Estevanato; Ricardo Brianezi Tiraboschi; Sonir Roberto Rauber Antonini; Valdair Francisco Muglia; Fernando Chahud; Lívia Mara Mermejo; José de Bessa Junior; Carlos Augusto Fernandes Molina

Hormone Research in Paediatrics Basel v. 95, n. 4, p. 347-353, 2022

Basel 2022

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3141169 Acervo Digital )(Acessar)

8
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)

9
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)

10
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)

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Data de Publicação 

De até
Refinar
  1. Antes de2011  (2)
  2. 2011Até2012  (6)
  3. 2013Até2015  (5)
  4. 2016Até2021  (5)
  5. Após 2021  (3)
  6. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.