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Refinado por: assunto: Hidroxilase (Deficiência) remover
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1
Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency
Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Long Term Glucocorticoid Exposition Does Not Play the Major Role in the Development of Obesity and Metabolic Syndrome in Classical Form of 21-Hydroxylase Deficiency

R. P. P. Moreira V. N Brito; L. G Gomes; G Madureira; B. B Mendonça; T. A. S. S Bachega; Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP) 2010 Costa do Sauípe, Bahia, Brazil) (21.

Hormone Research in Paediatrics Basel v. 74, n. suppl. 1, p. 12, res. 33, 2010

Basel 2010

Acesso online. A biblioteca também possui exemplares impressos.

2
Normal final height after use of cyproterone acetate in treatment of central precocious puberty secondary to 21-hydroxylase deficiency
Normal final height after use of cyproterone acetate in treatment of central precocious puberty secondary to 21-hydroxylase deficiency
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Normal final height after use of cyproterone acetate in treatment of central precocious puberty secondary to 21-hydroxylase deficiency

Larissa G. Gomes Enecy M. L Brenlha; Rosy C Ueti; Guiomar Madureira; Ivo J. P Arnhold; Berenice Bilharinho de Mendonça; Tania A. S. S Bachega; Annual Meeting of the Endocrine Society's (88. 2006 Boston)

Program & Abstracts Boston, 2006

Boston 2006

Localização: FM - Fac. Medicina    (FM BCSEP 245 2006 ) e outros locais(Acessar)

3
Improvement of hyperandrogenism and decrease of glucocorticoid dose with aging in female with 21-hydroxylase deficiency
Improvement of hyperandrogenism and decrease of glucocorticoid dose with aging in female with 21-hydroxylase deficiency
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Improvement of hyperandrogenism and decrease of glucocorticoid dose with aging in female with 21-hydroxylase deficiency

Sharon N. Admoni Enecy M. L Brenlha; Rosy C Ueti; Guiomar Madureira; Ana Elisa C Billerbeck; Ivo J. P Arnhold; Berenice Bilharinho de Mendonça; Tania A. S. S Bachega; Annual Meeting of the Endocrine Society's (88. 2006 Boston)

Program & Abstracts Boston, 2006

Boston 2006

Localização: FM - Fac. Medicina    (FM BCSEP 245 2006 ) e outros locais(Acessar)

4
Correlation between degree of external genitalia virilization and CAG repeats of the androgen receptor gene in DNA sample of peripheral leukocytes and pubic hair of women with 21-hydroxylase deficiency
Correlation between degree of external genitalia virilization and CAG repeats of the androgen receptor gene in DNA sample of peripheral leukocytes and pubic hair of women with 21-hydroxylase deficiency
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Correlation between degree of external genitalia virilization and CAG repeats of the androgen receptor gene in DNA sample of peripheral leukocytes and pubic hair of women with 21-hydroxylase deficiency

L. C. Kaupert A. E. C Billerbeck; V. N Brito; Berenice Bilharinho de Mendonça; T. A. S. S Bachega; Simpósio avanços em pesquisas médicas (3. 2007 São Paulo, SP); Symposium "Advances in Medical Research of the Medical Investigation Laboratories of Hospital das Clínicas da Faculdade de Medicina - USP" (3. 2007 São Paulo, SP)

Clinics São Paulo v. 62, supl. 3, p. S82, res. 276, 2007

São Paulo 2007

Item não circula. Consulte sua biblioteca.(Acessar)

5
Microconversion between pseudogene and CYP21A2 reduces the transcriptional activity causing nonclassical form of 21-hydroxylase deficiency
Microconversion between pseudogene and CYP21A2 reduces the transcriptional activity causing nonclassical form of 21-hydroxylase deficiency
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Microconversion between pseudogene and CYP21A2 reduces the transcriptional activity causing nonclassical form of 21-hydroxylase deficiency

R. S. Araujo A. S Barbosa; B. B Mendonça; C. J Lin; C. J Billerbeck; J. A. M Marcondes; T. A. S. S Bachega; Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP) (17. 2004 Angra dos Reis)

Journal of pediatric endocrinology and metabolism London v. 17, n. suppl.5, p. 1334, res. Oral 7, 2004

London 2004

Localização: FM - Fac. Medicina    (BCSEP 355 2004 ) e outros locais(Acessar)

6
Mielolipoma gigante bilateral associado à forma virilizante simples da deficiência da 21-hidroxilase
Mielolipoma gigante bilateral associado à forma virilizante simples da deficiência da 21-hidroxilase
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Mielolipoma gigante bilateral associado à forma virilizante simples da deficiência da 21-hidroxilase

L. A. Castroneves A. M Lerário; A. E. C Billerbeck; L. G Gomes; R. C Ueti; E. M Brenlha; G Madureira; B. B Mendonça; T. A. S. S Bachega; Congresso Brasileiro de Endocrinologia e Metabologia (27. 2006 Recife)

Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 50, n. 4, supl. 1, p. S510, res. P-024, 2006

São Paulo 2006

Item não circula. Consulte sua biblioteca.(Acessar)

7
Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a homozygous 25 BP duplication (NT 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon predicted by molecular modeling
Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a homozygous 25 BP duplication (NT 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon predicted by molecular modeling
Material Type:
Artigo 		Adicionar ao Meu Espaço

Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a homozygous 25 BP duplication (NT 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon predicted by molecular modeling

Regina M. Martin Paulo S Oliveira; Elaine M. F Costa; Ivo J. P Arnhold; Berenice Bilharinho de Mendonça

Arquivos brasileiros de endocrinologia e metabologia Rio de Janeiro v. 52, n. 8, p. 1317-1320, 2008

Rio de Janeiro 2008

Localização: FM - Fac. Medicina    (FM BCSEP 126 2008 )(Acessar)

8
The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency
The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency

Larissa G. Gomes Ningwu Huang; Berenice B Mendonça; Tania A. S. S Bachega; Walter L Miller

Journal of Clinical Endocrinology and Metabolism Philadelphia v. 93, n. 7, p. 2913-2916, 2008

Philadelphia 2008

Acesso online. A biblioteca também possui exemplares impressos.

9
Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Larissa G. Gomes Guiomar Madureira; Berenice B Mendonca; Tania A. S. S Bachega

Clinics São Paulo v. 68, n. 2, p. 147-151, 2013

São Paulo 2013

Localização: FM - Fac. Medicina    (BECEP 045 2013 )(Acessar)

10
Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia
Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia

Ricardo P. P. Moreira Sandra M Villares; Guiomar Madureira; Berenice B Mendonca; Tânia A. S. S Bachega

Hormone Research in Paediatrics Basel v. 80, n. 2, p. 111-118, 2013

Basel 2013

Localização: FM - Fac. Medicina    (BCSEP 418 2013 )(Acessar)

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Deste Autor:

  1. Bachega, T
  2. Mendonça, B
  3. Gomes, L
  4. Madureira, G
  5. Mendonca, B

Neste Assunto:

  1. Hiperplasia Suprarrenal Congênita
  2. Mutação Genética
  3. Fenótipos
  4. Polimorfismo
  5. Hipertensão

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

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