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Resultados de 11 a 20 de 33  para Produção Intelectual da USP

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Refinado por: Nome da Publicação: Clinical Endocrinology remover
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11
Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2
Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2
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Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2

Ana Teresa Prata Resende Clarissa Silva Martins; Ana Carolina Bueno; Ayrton Custódio Moreira; Maria Cristina Foss-Freitas; Margaret de Castro

Clinical Endocrinology West Sussex v. 91, n. 1, p. 94-103, 2019

West Sussex 2019

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3005934 Estantes Deslizantes )(Acessar)

12
Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism
Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism
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Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism

Beatriz R. Versiani Ericka Trarbach; Marcel Koenigkam-Santos; Antonio Carlos dos Santos; Lucila Leico Kagohara Elias; Ayrton Custódio Moreira; Ana Claudia Latronico; Margaret de Castro

Clinical Endocrinology Oxford v. 66, p. 173-179, 2007

Oxford 2007

Localização: FM - Fac. Medicina    (BCSEP 001 2007 ) e outros locais(Acessar)

13
Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls
Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls
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Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls

S. Marui Margaret de Castro; A. C Latronico; Lucila Leico Kagohara Elias; Ivo Jorge Prado Arnhold; Ayrton Custódio Moreira; B. B Mendonça

Clinical Endocrinology Oxford v. 52, p. 67-75, 2000

Oxford 2000

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1169896 )(Acessar)

14
Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene
Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene
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Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene

Paula Conde Lamparelli Elias Lucila Leico Kagohara Elias; Natalia Torres; Ayrton Custódio Moreira; José Antunes-Rodrigues; Margaret de Castro

Clinical Endocrinology Oxford v. 39, p. 511-518, 2003

Oxford 2003

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1345034 )(Acessar)

15
The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants the twin-pair synchrony
The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants the twin-pair synchrony
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The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants the twin-pair synchrony

Rodrigo José Custódio Carlos Eduardo Martinelli Júnior; Soraya Lopes Sader Milani; Aguinaldo Luiz Simões; Margaret de Castro; Ayrton Custódio Moreira

Clinical Endocrinology Oxford v. 66, n. 2, p. 192-197, 2007

Oxford 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1616873 )(Acessar)

16
Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone
Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone
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Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone

Patrícia Künzle Ribeiro Magalhães Gustavo Leopoldo Rodrigues Daré; Sandra Rodrigues dos Santos; Célia Regina Nogueira; Margaret de Castro; Léa Maria Zanini Maciel

Clinical Endocrinology Oxford v. 67, p. 748-753, 2007

Oxford 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1650547 )(Acessar)

17
Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene
Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene
Material Type:
Artigo 		Adicionar ao Meu Espaço

Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene

Paula Conde Lamparelli Elias Lucila Leico Kagohara Elias; Natalia Torres; Ayrton Custódio Moreira; José Antunes-Rodrigues; Margaret de Castro

Clinical Endocrinology Oxford v. 39, p. 511-518, 2003

Oxford 2003

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1345034 )(Acessar)

18
Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone
Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical features and genetic analysis of four brazilian kindreds with resistance to thyroid hormone

Patrícia Künzle Ribeiro Magalhães Gustavo Leopoldo Rodrigues Daré; Sandra Rodrigues dos Santos; Célia Regina Nogueira; Margaret de Castro; Léa Maria Zanini Maciel

Clinical Endocrinology Oxford v. 67, p. 748-753, 2007

Oxford 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1650547 )(Acessar)

19
The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants the twin-pair synchrony
The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants the twin-pair synchrony
Material Type:
Artigo 		Adicionar ao Meu Espaço

The emergence of the cortizol circadian rhythm in monozygotic and dizygotic twin infants the twin-pair synchrony

Rodrigo José Custódio Carlos Eduardo Martinelli Júnior; Soraya Lopes Sader Milani; Aguinaldo Luiz Simões; Margaret de Castro; Ayrton Custódio Moreira

Clinical Endocrinology Oxford v. 66, n. 2, p. 192-197, 2007

Oxford 2007

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 1616873 )(Acessar)

20
Glucocorticoid receptor gene polymorphism in ACTH-secreting pituitary tumours
Glucocorticoid receptor gene polymorphism in ACTH-secreting pituitary tumours
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Glucocorticoid receptor gene polymorphism in ACTH-secreting pituitary tumours

S. R. R. Antonini Ana Claudia Latronico; L. L. K Elias; A Cukier; H. R Machado; Bernardo Liberman; Berenice B Mendonça; Ayrton Custódio Moreira; M Castro

Clinical Endocrinology Oxford v. 57,n. 05, p. 657-662, 2002

Oxford 2002

Localização: FM - Fac. Medicina    (BCSEP 2002 219 )(Acessar)

Resultados de 11 a 20 de 33  para Produção Intelectual da USP

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Deste Autor:

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

Neste Assunto:

  1. Endocrinologia
  2. Pediatria
  3. Hipogonadismo
  4. Deleção De Genes
  5. Período Pós-Operatório

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

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