skip to main content
Idioma:
Resultados 1 2 next page
Mostrar Somente
Refinado por: Nome da Publicação: Journal of Clinical Endocrinology & Metabolism remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Brain MRI in girls with central precocious puberty a time for new approaches comment
Brain MRI in girls with central precocious puberty a time for new approaches comment
Material Type:
Artigo 		Adicionar ao Meu Espaço

Brain MRI in girls with central precocious puberty a time for new approaches comment

Ana Pinheiro Machado Canton Ana Claudia Latronico Xavier

Journal of clinical endocrinology & metabolism v. 106, n. 7, p. E2806-E2808, 2021

Washington 2021

Acesso online. A biblioteca também possui exemplares impressos.

2
Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma
Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma
Material Type:
Artigo 		Adicionar ao Meu Espaço

Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma

Gustavo F. C Fagundes Felipe Freitas-Castro; Lucas S Santana; Ana Caroline F Afonso; Janaina Petenuci; Mariana F. A Funari; Augusto G Guimaraes; Felipe L Ledesma; Ana Claudia Latronico Xavier; Berenice Bilharinho de Mendonca

Journal of clinical endocrinology & metabolism v. 108, n. 8, p. 2105-2114, 2023

Washington 2023

Acesso online. A biblioteca também possui exemplares impressos.

3
Clinical and Genetic Characterization of Familial Central Precocious Puberty
Clinical and Genetic Characterization of Familial Central Precocious Puberty
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical and Genetic Characterization of Familial Central Precocious Puberty

Flavia Rezende Tinano Ana Pinheiro Machado Canton; Luciana Ribeiro Montenegro; Andrea de Castro Leal; Aline G Faria; Carlos E Seraphim; Raja Brauner; Alexander Augusto de Lima Jorge; Berenice Bilharinho de Mendonca; Ana Claudia Latronico Xavier

Journal of clinical endocrinology & metabolism v. 108, n. 7, p. 1758-1767, 2023

Washington 2023

Acesso online. A biblioteca também possui exemplares impressos.

4
Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination
Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination

John C Magnotto Alessandra Mancini; Keisha Bird; Luciana Montenegro; Filiz Tutunculer; Sidney A Pereira; Vitoria Simas; Leonardo Garcia; Stephanie A Roberts; Ana Claudia Latronico Xavier

Journal of clinical endocrinology & metabolism v. 108, n. 7, p. 1646-1656, 2023

Washington 2023

Acesso online. A biblioteca também possui exemplares impressos.

5
Response to Letter to the Editor ""IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy"" [Carta]
Response to Letter to the Editor ""IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy"" [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Response to Letter to the Editor ""IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy"" [Carta]

Gabriela A Vasques Alexander Augusto de Lima Jorge

Journal of clinical endocrinology & metabolism v. 104, n. 11, p. 5115-5116, 2019

Washington 2019

Acesso online. A biblioteca também possui exemplares impressos.

6
PTPN11 (Protein tyrosine phosphatase, nonreceptor type 11) mutations and response to growth hormone therapy in children with Noonan syndrome
PTPN11 (Protein tyrosine phosphatase, nonreceptor type 11) mutations and response to growth hormone therapy in children with Noonan syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

PTPN11 (Protein tyrosine phosphatase, nonreceptor type 11) mutations and response to growth hormone therapy in children with Noonan syndrome

Lize V. Ferreira Silvia A. L Souza; Ivo J. P Arnhold; Berenice Bilharinho Mendonça; Alexander A. L Jorge

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 90, n. 9, p. 5156-5160, 2005

Philadelphia 2005

Localização: FM - Fac. Medicina    (FM BCSEP 259 2005 )(Acessar)

7
The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
Material Type:
Artigo 		Adicionar ao Meu Espaço

The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

Viviane Pardo Jussara Vono-Toniolo; Ileana G. S Rubio; Meyer Knobel; Roberta F Possato; Hector M Targovnik; Peter Kopp; Geraldo Medeiros-Neto

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 94, n. 8, p. 2938-2944, 2009

Philadelphia 2009

Acesso online. A biblioteca também possui exemplares impressos.

8
IHH gene mutations causing short stature with nonspecific skeletal abnormalities and response to growth hormone therapy
IHH gene mutations causing short stature with nonspecific skeletal abnormalities and response to growth hormone therapy
Material Type:
Artigo 		Adicionar ao Meu Espaço

IHH gene mutations causing short stature with nonspecific skeletal abnormalities and response to growth hormone therapy

Gabriela A. Vasques Frederico Moraes Ferreira; Alexander Augusto de Lima Jorge

Journal of clinical endocrinology & metabolism v. 103, n. 2, p. 604-614, 2018

Cary 2018

Item não circula. Consulte sua biblioteca.(Acessar)

9
PTPN11 (Protein tyrosine phosphatase, nonreceptor type 11) mutations and response to growth hormone therapy in children with Noonan syndrome
PTPN11 (Protein tyrosine phosphatase, nonreceptor type 11) mutations and response to growth hormone therapy in children with Noonan syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

PTPN11 (Protein tyrosine phosphatase, nonreceptor type 11) mutations and response to growth hormone therapy in children with Noonan syndrome

Lize V. Ferreira Silvia A. L Souza; Ivo J. P Arnhold; Berenice Bilharinho Mendonça; Alexander A. L Jorge

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 90, n. 9, p. 5156-5160, 2005

Philadelphia 2005

Localização: FM - Fac. Medicina    (FM BCSEP 259 2005 )(Acessar)

10
The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
Material Type:
Artigo 		Adicionar ao Meu Espaço

The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

Viviane Pardo Jussara Vono-Toniolo; Ileana G. S Rubio; Meyer Knobel; Roberta F Possato; Hector M Targovnik; Peter Kopp; Geraldo Medeiros-Neto

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 94, n. 8, p. 2938-2944, 2009

Philadelphia 2009

Acesso online. A biblioteca também possui exemplares impressos.

Resultados 1 2 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Mostrar Somente

  1. Disponível na Biblioteca (13)
  2. Recursos Online (9)

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Mendonça, B
  2. Xavier, A
  3. Jorge, A
  4. Montenegro, L
  5. Pardo, V

Neste Assunto:

  1. Mutação Genética
  2. Puberdade Precoce
  3. Crianças
  4. Neoplasias Das Glândulas Suprarrenais
  5. Genótipos

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

Buscando em bases de dados remotas. Favor aguardar.