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Refinado por: Nome da Publicação: The Journal of Clinical Endocrinology & Metabolism remover
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1
The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome
The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome

Adriana F. Braz Everlayny F Costalonga; Luciana Ribeiro Montenegro; Ericka B Trarbach; Sonir Roberto Rauber Antonini; Alexsandra C Malaquias; Ester Silveira Ramos; Berenice Bilharinho Mendonca; Ivo J. P Arnhold; Alexander Augusto de Lima Jorge

The journal of clinical endocrinology & metabolism Springfield v. 97, n. 4, p. E671-E677, 2012

Springfield 2012

Localização: FM - Fac. Medicina    (BCSEP 067 2012 ) e outros locais(Acessar)

2
The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome
The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome

Adriana F. Braz Everlayny F Costalonga; Luciana Ribeiro Montenegro; Ericka B Trarbach; Sonir Roberto Rauber Antonini; Alexsandra C Malaquias; Ester Silveira Ramos; Berenice Bilharinho Mendonca; Ivo J. P Arnhold; Alexander Augusto de Lima Jorge

The journal of clinical endocrinology & metabolism Springfield v. 97, n. 4, p. E671-E677, 2012

Springfield 2012

Localização: FM - Fac. Medicina    (BCSEP 067 2012 ) e outros locais(Acessar)

3
Potential effects of alendronate on fibroblast growth factor 23 levels and effective control of hypercalciuria in an adult with jansen's metaphyseal chondrodysplasia
Potential effects of alendronate on fibroblast growth factor 23 levels and effective control of hypercalciuria in an adult with jansen's metaphyseal chondrodysplasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Potential effects of alendronate on fibroblast growth factor 23 levels and effective control of hypercalciuria in an adult with jansen's metaphyseal chondrodysplasia

Laura Onuchic Bruno Ferraz de Souza; Berenice Bilharinho Mendonca; Pedro Henrique S Correa; Regina M Martin

The journal of clinical endocrinology & metabolism Springfield v. 97, n. 4, p. 1098-1103

Springfield 2012

Localização: FM - Fac. Medicina    (BCSEP 067 2012 )(Acessar)

4
Potential effects of alendronate on fibroblast growth factor 23 levels and effective control of hypercalciuria in an adult with jansen's metaphyseal chondrodysplasia
Potential effects of alendronate on fibroblast growth factor 23 levels and effective control of hypercalciuria in an adult with jansen's metaphyseal chondrodysplasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Potential effects of alendronate on fibroblast growth factor 23 levels and effective control of hypercalciuria in an adult with jansen's metaphyseal chondrodysplasia

Laura Onuchic Bruno Ferraz de Souza; Berenice Bilharinho Mendonca; Pedro Henrique S Correa; Regina M Martin

The journal of clinical endocrinology & metabolism Springfield v. 97, n. 4, p. 1098-1103

Springfield 2012

Localização: FM - Fac. Medicina    (BCSEP 067 2012 )(Acessar)

5
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)

6
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)

7
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)

8
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:
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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)

9
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
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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)

10
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
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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)

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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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