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Refinado por: Nome da Publicação: The Journal of Clinical Endocrinology & Metabolism remover
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1
Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations

Tânia A. S. S. Bachega Enecy M. L Brenlha; Ana E. C Billerbeck; José A. M Marcondes; Guiomar Madureira; Ivo J. P Arnhold; Berenice B Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 2, p. 786-790, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)

2
Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect
Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect
Material Type:
Artigo 		Adicionar ao Meu Espaço

Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect

Ana Elisa C. Billerbeck Berenice B Mendonça; Emilia M Pinto; Guiomar Madureira; Ivo J. P Arnhold; Tânia A. S. S Bachega

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 9, p. 4314-4317, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)

3
Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes
Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes

Maria Geralda F. Osorio Suemi Marui; Alexander A. L Jorge; Ana C Latronico; Leonard S. S Lo; Claudia C Leite; Vivian Estefan; Berenice B Mendonça; Ivo J. P Arnhold

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 11, p. 5076-5084, 2002

Bethesda 2002

Localização: FMRAD - Fac. Medicina-Depto. Radiologia    (SEP 23/2002 )(Acessar)

4
Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH receptor gene
Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH receptor gene
Material Type:
Artigo 		Adicionar ao Meu Espaço

Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH receptor gene

Alexander A. Jorge Silvia C Souza; Ivo J Arnhold; Berenice B Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 2, p. 469-472, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)

5
Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH receptor gene
Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH receptor gene
Material Type:
Artigo 		Adicionar ao Meu Espaço

Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH receptor gene

Alexander A. Jorge Silvia C Souza; Ivo J Arnhold; Berenice B Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 2, p. 469-472, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)

6
Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect
Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect
Material Type:
Artigo 		Adicionar ao Meu Espaço

Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect

Ana Elisa C. Billerbeck Berenice B Mendonça; Emilia M Pinto; Guiomar Madureira; Ivo J. P Arnhold; Tânia A. S. S Bachega

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 9, p. 4314-4317, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)

7
Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
Material Type:
Artigo 		Adicionar ao Meu Espaço

Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations

Tânia A. S. S. Bachega Enecy M. L Brenlha; Ana E. C Billerbeck; José A. M Marcondes; Guiomar Madureira; Ivo J. P Arnhold; Berenice B Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 2, p. 786-790, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)

8
Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes
Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes
Material Type:
Artigo 		Adicionar ao Meu Espaço

Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes

Maria Geralda F. Osorio Suemi Marui; Alexander A. L Jorge; Ana C Latronico; Leonard S. S Lo; Claudia C Leite; Vivian Estefan; Berenice B Mendonça; Ivo J. P Arnhold

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 11, p. 5076-5084, 2002

Bethesda 2002

Localização: FMRAD - Fac. Medicina-Depto. Radiologia    (SEP 23/2002 )(Acessar)

9
Cushing's syndrome secondary to adrenocorticotropin-independente macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene
Cushing's syndrome secondary to adrenocorticotropin-independente macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cushing's syndrome secondary to adrenocorticotropin-independente macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene

Maria Candida Barisson Villares Fragoso Sorahia Domenice; Ana Claudia Latronico; Regina Matsunaga Martin; Maria Adelaide Albergaria Pereira; Maria Claudia Nogueira Zerbini; Antonio Marmo Lucon; Berenice Bilharinho Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 88, n. 5, p. 2147-2151, 2003

Bethesda 2003

Localização: FM - Fac. Medicina    (FM-BCBIB )(Acessar)

10
Cushing's syndrome secondary to adrenocorticotropin-independente macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene
Cushing's syndrome secondary to adrenocorticotropin-independente macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cushing's syndrome secondary to adrenocorticotropin-independente macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene

Maria Candida Barisson Villares Fragoso Sorahia Domenice; Ana Claudia Latronico; Regina Matsunaga Martin; Maria Adelaide Albergaria Pereira; Maria Claudia Nogueira Zerbini; Antonio Marmo Lucon; Berenice Bilharinho Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 88, n. 5, p. 2147-2151, 2003

Bethesda 2003

Localização: FM - Fac. Medicina    (FM-BCBIB )(Acessar)

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Deste Autor:

  1. Mendonça, B
  2. Arnhold, I
  3. Jorge, A
  4. Latronico, A
  5. Bachega, T

Neste Assunto:

  1. Genética Molecular
  2. Endocrinologia
  3. Mutação Genética
  4. Biologia Molecular
  5. Protocolos Clínicos

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

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