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Resultados de 1 a 10 de 21  para Produção Intelectual da USP

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1
Characterization of adrenocorticotropin secretion in a patient with 17 alfa - hydroxicase deficience
Characterization of adrenocorticotropin secretion in a patient with 17 alfa - hydroxicase deficience
Material Type:
Artigo 		Adicionar ao Meu Espaço

Characterization of adrenocorticotropin secretion in a patient with 17 alfa - hydroxicase deficience

Ayrton Custódio Moreira A M O Leal; M C Castro

v. 71, p. 86, 1990 Journal of Clinical Endocrinology and Metabolism

1990

Item não circula. Consulte sua biblioteca.(Acessar)

2
Characterization of adrenocorticotropin secretion in a patient with 17 alfa - hydroxicase deficience
Characterization of adrenocorticotropin secretion in a patient with 17 alfa - hydroxicase deficience
Material Type:
Artigo 		Adicionar ao Meu Espaço

Characterization of adrenocorticotropin secretion in a patient with 17 alfa - hydroxicase deficience

Ayrton Custódio Moreira A M O Leal; M C Castro

v. 71, p. 86, 1990 Journal of Clinical Endocrinology and Metabolism

1990

Item não circula. Consulte sua biblioteca.(Acessar)

3
Letter to the Editor. [Carta] comments on "LGR5 activates noncanonical Wnt signaling and inhibits aldosterone production in the human adrenal" by Shaikh L. H., et al
Letter to the Editor. [Carta] comments on "LGR5 activates noncanonical Wnt signaling and inhibits aldosterone production in the human adrenal" by Shaikh L. H., et al
Material Type:
Artigo 		Adicionar ao Meu Espaço

Letter to the Editor. [Carta] comments on "LGR5 activates noncanonical Wnt signaling and inhibits aldosterone production in the human adrenal" by Shaikh L. H., et al

Letícia Ferro Leal Livia M Mermejo; Clarissa S Martins; Sonir Roberto Rauber Antonini; Margaret de Castro

Journal of Clinical Endocrinology and Metabolism Chevy Chase v. 100, n. 12, p. L125, 2015

Chevy Chase 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2760678 Estantes Deslizantes )(Acessar)

4
Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome
Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome

Paula Conde Lamparelli Elias Edson Zangiacomi Martinez; Bruno F. C Barone; Livia M Mermejo; Margaret Castro; Ayrton Custódio Moreira

Journal of Clinical Endocrinology and Metabolism Chevy Chase v. 99, n. 6, p. 2045-2051, 2014

Chevy Chase 2014

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2692429 Estantes Deslizantes )(Acessar)

5
Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients
Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients

Fernanda C. Soardi Junia Y Penachioni; Giselle Z Justo; Tânia A. S. S Bachega; Marlene Inácio; Berenice Bilharinho de Mendonça; Margaret de Castro; Maricilda P. de Mello

Journal of clinical endocrinology and metabolism Springfield v. 94, n. 9, p. 3481-3485, 2009

Springfield 2009

Localização: FM - Fac. Medicina    (FM BCSEP 074 2009 ) e outros locais(Acessar)

6
A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome
A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome

Ana Carolina Bueno Kai Sun; Clarissa Silva Martins; Jorge Elias Júnior; Wallace Miranda; Caroline Tao; Maria Cristina Foss-Freitas; Marco Antonio Barbieri; Heloisa Bettiol; Margaret de Castro; Philipp E Scherer; Sonir Roberto Rauber Antonini

Journal of Clinical Endocrinology and Metabolism Chevy Chase v. 99 n.4, p. E683-E693, 2014

Chevy Chase 2014

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2647425 Estantes Deslizantes )(Acessar)

7
Landscape of familial isolated and young-onset pituitary adenomas prospective diagnosis in AIP mutation carriers
Landscape of familial isolated and young-onset pituitary adenomas prospective diagnosis in AIP mutation carriers
Material Type:
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Landscape of familial isolated and young-onset pituitary adenomas prospective diagnosis in AIP mutation carriers

Laura C. Hernández-Ramirez Plamena Gabrovska; Judit Dénes; Karen Stals; Giampaolo Trivellin; Daniel Tilley; Francesco Ferraú; Jane Evanson; Sian Ellard; Ashley B Grossman; Federico Roncaroli; Mônica R Gadelha; Márta Korbonits; Margaret de Castro

Journal of Clinical Endocrinology and Metabolism Chevy Chase v. 100, n. 9, p. E1242-E1254, 2015

Chevy Chase 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2760685 Estantes Deslizantes )(Acessar)

8
Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients
Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients

Fernanda C. Soardi Junia Y Penachioni; Giselle Z Justo; Tânia A. S. S Bachega; Marlene Inácio; Berenice Bilharinho de Mendonça; Margaret de Castro; Maricilda P. de Mello

Journal of clinical endocrinology and metabolism Springfield v. 94, n. 9, p. 3481-3485, 2009

Springfield 2009

Localização: FM - Fac. Medicina    (FM BCSEP 074 2009 ) e outros locais(Acessar)

9
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome

Ana Paula Abreu Ericka Barbosa Trarbach; Margaret de Castro; Elaine Maria Frade Costa; Beatriz Versiani; Maria Tereza Matias Baptista; Heraldo Mendes Garmes; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 93, n. 10, p. 4113-4118, 2008

Philadelphia 2008

Localização: FM - Fac. Medicina    (BCSEP 230 2008 ) e outros locais(Acessar)

10
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome

Ana Paula Abreu Ericka Barbosa Trarbach; Margaret de Castro; Elaine Maria Frade Costa; Beatriz Versiani; Maria Tereza Matias Baptista; Heraldo Mendes Garmes; Berenice Bilharinho Mendonça; Ana Claudia Latronico

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 93, n. 10, p. 4113-4118, 2008

Philadelphia 2008

Localização: FM - Fac. Medicina    (BCSEP 230 2008 ) e outros locais(Acessar)

Resultados de 1 a 10 de 21  para Produção Intelectual da USP

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Deste Autor:

  1. Castro, M
  2. Moreira, A
  3. Antonini, S
  4. Latronico, A
  5. Mermejo, L

Neste Assunto:

  1. Mutação Genética
  2. Fenótipos
  3. Crianças
  4. Genética
  5. Expressão Gênica

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

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