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1
Auxological study of patients with SHOX defect and the response of combined treatment with recombinant growth hormone and gonadotropin-releasing hormone analog
Auxological study of patients with SHOX defect and the response of combined treatment with recombinant growth hormone and gonadotropin-releasing hormone analog
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Auxological study of patients with SHOX defect and the response of combined treatment with recombinant growth hormone and gonadotropin-releasing hormone analog

Debora C. C. Liborio Silvia C Souza; Mirian Y Nishi; Ana Elisa C Billerbeck; Ivo J. P Arnhold; Berenice Bilharinho de Mendonça; Alexander A. L Jorge; 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)

2
Role of luteinizing hormone (LH) isoforms and allelie variants in hypogonadotropic hypogonadism (HH)
Role of luteinizing hormone (LH) isoforms and allelie variants in hypogonadotropic hypogonadism (HH)
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Artigo de Congresso 		Adicionar ao Meu Espaço

Role of luteinizing hormone (LH) isoforms and allelie variants in hypogonadotropic hypogonadism (HH)

Karina Berger Ana Elisa Billerbeck; Antonio Carlos Magnanelli; Valeria Sutti Nunes; Elaine Maria Frade Costa; Ivo Jorge Prado Arnhold; Berenice Bilharinho de Mendonça; ENDO 06 - Annual Meeting the endocrine society's (88. 2006 Boston)

Resumos Boston p. 855, res. P3-837, 2006

Boston 2006

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

3
Role of the IGF1 gene (CA) repeats on birth length and weight, catch up growth and IGF-1 serum level in brazilian SGA infants
Role of the IGF1 gene (CA) repeats on birth length and weight, catch up growth and IGF-1 serum level in brazilian SGA infants
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Artigo de Congresso 		Adicionar ao Meu Espaço

Role of the IGF1 gene (CA) repeats on birth length and weight, catch up growth and IGF-1 serum level in brazilian SGA infants

Rocio R. D. Coletta Ricardo M Garcia; Alexander A. L Jorge; Margaret Boguszewski; Emilia M Pinto; Ana E. C Billerbeck; Paulo Pachi; Carlos A Longui; Elaine M. F Costa; Berenice Bilharinho de Mendonça; 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
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)

5
MEN 1 gene is not implicated in adrenal hyperplasia associated with multiple endocrine neoplasia type 1
MEN 1 gene is not implicated in adrenal hyperplasia associated with multiple endocrine neoplasia type 1
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

MEN 1 gene is not implicated in adrenal hyperplasia associated with multiple endocrine neoplasia type 1

Marcia Helena S. Costa Emilia M Pinto; Ana Elisa Billerbeck; Berenice Bilharinho de Mendonça; Delmar Muniz Junior; S. P. A Toledo (Sérgio Pereira de Almeida); Maria Candida B. V Fragoso; ENDO 06 - Annual Meeting the endocrine society's (88. 2006 Boston)

Resumos Boston p. 799, res. P3-637, 2006

Boston 2006

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

6
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
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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)

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