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1
Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature
Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature

Alexander A. L Jorge Silvia C. A. L Souza; Ivo J. P Arnhold; Berenice Bilharinho Mendonca; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)

Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p.78A. res. PI-461, 2001

Philadelphia 2001

Item não circula. Consulte sua biblioteca.(Acessar)

2
Frequency of genetic polymorphisms of PXR gene in the Brazilian population
Frequency of genetic polymorphisms of PXR gene in the Brazilian population
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Frequency of genetic polymorphisms of PXR gene in the Brazilian population

Moreira, Ricardo P. P.; Jorge, Alexander A. L.; Mendonca, Berenice B.; Bachega, Tânia A. S. S.

Clinics; v. 66 n. 6 (2011); 1041-1044

Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo 2011-01-01

Acesso online

3
Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development
Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development
Material Type:
Artigo 		Adicionar ao Meu Espaço

Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development

Montenegro, Luciana R.; Lerário, Antônio M.; Nishi, Miriam Y.; Jorge, Alexander A. L.; Mendonca, Berenice B.

Clinics; v. 76 (2021); e2052

Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo 2021-11-09

Acesso online

4
Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3
Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3

Alexander A. L. Jorge Chin J Lin; Silvia C. A. L Souza; Ivo Jorge Prado arnhold; Berenice Bilharinho Mendonca; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)

Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 69A. res. P1-407, 2001

Philadelphia 2001

Item não circula. Consulte sua biblioteca.(Acessar)

5
Role of GLI2 in hypopituitarism phenotype
Role of GLI2 in hypopituitarism phenotype
Material Type:
Artigo 		Adicionar ao Meu Espaço

Role of GLI2 in hypopituitarism phenotype

Ivo J. P. Arnhold Marcela M França; Luciani R Carvalho; Berenice B Mendonca; Alexander A. L Jorge

Journal of Molecular Endocrinology Bristol v. 54, n. 3, p. R141-R150, 2015

Bristol 2015

Acesso online. A biblioteca também possui exemplares impressos.

6
Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Moreira, Ricardo P. P.; Jorge, Alexander A. L.; Gomes, Larissa G.; Kaupert, Laura C.; Massud Filho, João; Mendonca, Berenice B.; Bachega, Tânia A. S. S.

Clinics; v. 66 n. 8 (2011); 1361-1366

Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo 2011-01-01

Acesso online

7
Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Ricardo P. P. Moreira Alexander A. L Jorge; Larissa G Gomes; Laura C Kaupert; João Massud Filho; Berenice B Mendonca; Tânia A. S. S Bachega

Clinics São Paulo v. 66, n. 8, p. 1361-1365, 2011

São Paulo 2011

Localização: FM - Fac. Medicina    (BCSEP 066 2011 )(Acessar)

8
Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients
Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients
Material Type:
Artigo 		Adicionar ao Meu Espaço

Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients

Lize V. Ferreira Silvia C. A. L Souza; Luciana R Montenegro; Alexsandra C Malaquias; Ivo J. P Arnhold; Berenice B Mendonca; Alexander A. L Jorge

Clinical Endocrinology Oxford v. 69, n. 3, p. 426-431, 2008

Oxford 2008

Localização: FM - Fac. Medicina    (BCSEP 227 2008 )(Acessar)

9
Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA)
Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA)
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Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA)

Mariana F. A. Funari Alexander A. L Jorge; Emilia M Pinto; Ivo J. P Arnhold; Berenice B Mendonca; Mirian Y Nishi

Arquivos Brasileiros de Endocrinologia e Metabologia São Paulo v. 52, n. 8, p. 1382-1387, 2008

São Paulo 2008

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

10
The −202 A Allele of Insulin-Like Growth Factor Binding Protein-3 (IGFBP3) Promoter Polymorphism Is Associated with Higher IGFBP-3 Serum Levels and Better Growth Response to Growth Hormone Treatment in Patients with Severe Growth Hormone Deficiency
The −202 A Allele of Insulin-Like Growth Factor Binding Protein-3 (IGFBP3) Promoter Polymorphism Is Associated with Higher IGFBP-3 Serum Levels and Better Growth Response to Growth Hormone Treatment in Patients with Severe Growth Hormone Deficiency
Material Type:
Artigo 		Adicionar ao Meu Espaço

The −202 A Allele of Insulin-Like Growth Factor Binding Protein-3 (IGFBP3) Promoter Polymorphism Is Associated with Higher IGFBP-3 Serum Levels and Better Growth Response to Growth Hormone Treatment in Patients with Severe Growth Hormone Deficiency

Everlayny Fiorot Costalonga Sonir R Antonini; Gil Guerra-Junior; Berenice Bilharinho Mendonca; Ivo J. P Arnhold; Alexander A. L Jorge

Journal of Clinical Endocrinology & Metabolism Philadelphia v. 94, n. 2, p. 588-595, 2009

Philadelphia 2009

Acesso online. A biblioteca também possui exemplares impressos.

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