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Artigo de periodico
The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene (2016)
Moura-Massari, Vivian Oliveira; Cunha, Flávia Siqueira; Gomes, Larissa Garcia; Gomes, Diogo Bugano Diniz; Marcondes, José Antônio Miguel; Madureira, Guiomar; Mendonca, Berenice Bilharinho de ; Bachega, Tania Aparecida Sartori Sanchez
Source: PloS One. Unidade: FM
Subjects: POLIMORFISMO, HIDROXILASE (DEFICIÊNCIA), RECEPTORES ANDROGÊNICOS
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ABNT
MOURA-MASSARI, Vivian Oliveira et al. The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene. PloS One, v. 11, n. 2, p. 13 , 2016Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0148548. Acesso em: 20 fev. 2026.
APA
Moura-Massari, V. O., Cunha, F. S., Gomes, L. G., Gomes, D. B. D., Marcondes, J. A. M., Madureira, G., et al. (2016). The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene. PloS One, 11( 2), 13 . doi:10.1371/journal.pone.0148548
NLM
Moura-Massari VO, Cunha FS, Gomes LG, Gomes DBD, Marcondes JAM, Madureira G, Mendonca BB de, Bachega TASS. The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene [Internet]. PloS One. 2016 ; 11( 2): 13 .[citado 2026 fev. 20 ] Available from: https://doi.org/10.1371/journal.pone.0148548
Vancouver
Moura-Massari VO, Cunha FS, Gomes LG, Gomes DBD, Marcondes JAM, Madureira G, Mendonca BB de, Bachega TASS. The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene [Internet]. PloS One. 2016 ; 11( 2): 13 .[citado 2026 fev. 20 ] Available from: https://doi.org/10.1371/journal.pone.0148548
Artigo de periodico
Fatty acid 2-hydroxylase deficiency: Clinical features and brain iron accumulation (2015)
Pedroso, Jose Luiz; Handfas, Benjamin W.; Abrahão, Agessandro; Kok, Fernando; Barsottini, Orlando G. P.; Oliveira, Acary S. Bulle
Source: Neurology. Unidade: FM
Subjects: TÉCNICAS BIOLÓGICAS, DOENÇAS CEREBRAIS (DIAGNÓSTICO), FERRO, HIDROXILASE (DEFICIÊNCIA), IMAGEM POR RESSONÂNCIA MAGNÉTICA
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ABNT
PEDROSO, Jose Luiz et al. Fatty acid 2-hydroxylase deficiency: Clinical features and brain iron accumulation. Neurology, v. 84, n. 9, p. 960-961, 2015Tradução . . Disponível em: https://doi.org/10.1212/wnl.0000000000001316. Acesso em: 20 fev. 2026.
APA
Pedroso, J. L., Handfas, B. W., Abrahão, A., Kok, F., Barsottini, O. G. P., & Oliveira, A. S. B. (2015). Fatty acid 2-hydroxylase deficiency: Clinical features and brain iron accumulation. Neurology, 84( 9), 960-961. doi:10.1212/wnl.0000000000001316
NLM
Pedroso JL, Handfas BW, Abrahão A, Kok F, Barsottini OGP, Oliveira ASB. Fatty acid 2-hydroxylase deficiency: Clinical features and brain iron accumulation [Internet]. Neurology. 2015 ; 84( 9): 960-961.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1212/wnl.0000000000001316
Vancouver
Pedroso JL, Handfas BW, Abrahão A, Kok F, Barsottini OGP, Oliveira ASB. Fatty acid 2-hydroxylase deficiency: Clinical features and brain iron accumulation [Internet]. Neurology. 2015 ; 84( 9): 960-961.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1212/wnl.0000000000001316
Artigo de periodico
Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia (2013)
Moreira, Ricardo P. P.; Villares, Sandra M.; Madureira, Guiomar; Mendonca, Berenice B.; Bachega, Tânia A. S. S.
Source: Hormone Research in Paediatrics. Unidade: FM
Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA, JOVENS, PACIENTES, OBESIDADE (MORTALIDADE), ÍNDICE DE MASSA CORPORAL, DOENÇAS HEREDITÁRIAS, HIDROXILASE (DEFICIÊNCIA)
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ABNT
MOREIRA, Ricardo P. P. et al. Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia. Hormone Research in Paediatrics, v. 80, n. 2, p. 111-118, 2013Tradução . . Disponível em: http://www.karger.com/Article/Pdf/353762. Acesso em: 20 fev. 2026.
APA
Moreira, R. P. P., Villares, S. M., Madureira, G., Mendonca, B. B., & Bachega, T. A. S. S. (2013). Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia. Hormone Research in Paediatrics, 80( 2), 111-118. doi:10.1159/000353762
NLM
Moreira RPP, Villares SM, Madureira G, Mendonca BB, Bachega TASS. Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 111-118.[citado 2026 fev. 20 ] Available from: http://www.karger.com/Article/Pdf/353762
Vancouver
Moreira RPP, Villares SM, Madureira G, Mendonca BB, Bachega TASS. Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 111-118.[citado 2026 fev. 20 ] Available from: http://www.karger.com/Article/Pdf/353762
Artigo de periodico
Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2013)
Gomes, Larissa G.; Madureira, Guiomar; Mendonca, Berenice B.; Bachega, Tania A. S. S.
Source: Clinics. Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), GENÉTICA, ESTUDOS RETROSPECTIVOS, HIPERPLASIAS (DIAGNÓSTICO), RADIOIMUNOENSAIO
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ABNT
GOMES, Larissa G. et al. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, v. 68, n. 2, p. 147-151, 2013Tradução . . Disponível em: https://doi.org/10.6061/CLINICS/2013(02)OA05. Acesso em: 20 fev. 2026.
APA
Gomes, L. G., Madureira, G., Mendonca, B. B., & Bachega, T. A. S. S. (2013). Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, 68( 2), 147-151. doi:10.6061/CLINICS/2013(02)OA05
NLM
Gomes LG, Madureira G, Mendonca BB, Bachega TASS. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinics. 2013 ; 68( 2): 147-151.[citado 2026 fev. 20 ] Available from: https://doi.org/10.6061/CLINICS/2013(02)OA05
Vancouver
Gomes LG, Madureira G, Mendonca BB, Bachega TASS. Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinics. 2013 ; 68( 2): 147-151.[citado 2026 fev. 20 ] Available from: https://doi.org/10.6061/CLINICS/2013(02)OA05
Trabalho de evento-resumo periodico
Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD) (2012)
Coeli, F.; Turatti, W.; Elias, P.; Martinelli Junior, Carlos Eduardo; Moreira, Ayrton Custódio; Antonini, Sonir Roberto Rauber; Castro, Margaret de
Source: Endocrine Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FMRP
Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA, HIDROXILASE (DEFICIÊNCIA)
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ABNT
COELI, F. et al. Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD). Endocrine Abstracts. Woodlands: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 20 fev. 2026. , 2012
APA
Coeli, F., Turatti, W., Elias, P., Martinelli Junior, C. E., Moreira, A. C., Antonini, S. R. R., & Castro, M. de. (2012). Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD). Endocrine Abstracts. Woodlands: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Coeli F, Turatti W, Elias P, Martinelli Junior CE, Moreira AC, Antonini SRR, Castro M de. Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD). Endocrine Abstracts. 2012 ; 29[citado 2026 fev. 20 ]
Vancouver
Coeli F, Turatti W, Elias P, Martinelli Junior CE, Moreira AC, Antonini SRR, Castro M de. Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD). Endocrine Abstracts. 2012 ; 29[citado 2026 fev. 20 ]
Artigo de periodico
Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review (2011)
Marchini, Giovanni Scala; Cocuzza, Marcello; Pagani, Rodrigo; Torricelli, Fábio César; Hallak, Jorge; Srougi, Miguel
Source: São Paulo Medical Journal. Unidade: FM
Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA, IMAGEM POR RESSONÂNCIA MAGNÉTICA, INFERTILIDADE MASCULINA, TESTÍCULO (CIRURGIA), ESTUDO DE CASO, MICROCIRURGIA, HIDROXILASE (DEFICIÊNCIA), SEGUIMENTOS
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ABNT
MARCHINI, Giovanni Scala et al. Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review. São Paulo Medical Journal, v. 129, n. 5, p. 346-351, 2011Tradução . . Disponível em: https://doi.org/10.1590/s1516-31802011000500010. Acesso em: 20 fev. 2026.
APA
Marchini, G. S., Cocuzza, M., Pagani, R., Torricelli, F. C., Hallak, J., & Srougi, M. (2011). Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review. São Paulo Medical Journal, 129( 5), 346-351. doi:10.1590/s1516-31802011000500010
NLM
Marchini GS, Cocuzza M, Pagani R, Torricelli FC, Hallak J, Srougi M. Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review [Internet]. São Paulo Medical Journal. 2011 ; 129( 5): 346-351.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/s1516-31802011000500010
Vancouver
Marchini GS, Cocuzza M, Pagani R, Torricelli FC, Hallak J, Srougi M. Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review [Internet]. São Paulo Medical Journal. 2011 ; 129( 5): 346-351.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/s1516-31802011000500010
Artigo de periodico
Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2011)
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.
Source: Clinics. Unidade: FM
Subjects: FARMACOGENÉTICA, HIPERPLASIA SUPRARRENAL CONGÊNITA, HIDROXILASE (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, Ricardo P. P. et al. Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, v. 66, n. 8, p. 1361-1365, 2011Tradução . . Disponível em: https://doi.org/10.1590/S1807-59322011000800009. Acesso em: 20 fev. 2026.
APA
Moreira, R. P. P., Jorge, A. A. L., Gomes, L. G., Kaupert, L. C., Massud Filho, J., Mendonca, B. B., & Bachega, T. A. S. S. (2011). Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics, 66( 8), 1361-1365. doi:10.1590/S1807-59322011000800009
NLM
Moreira RPP, Jorge AAL, Gomes LG, Kaupert LC, Massud Filho J, Mendonca BB, Bachega TASS. Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinics. 2011 ; 66( 8): 1361-1365.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/S1807-59322011000800009
Vancouver
Moreira RPP, Jorge AAL, Gomes LG, Kaupert LC, Massud Filho J, Mendonca BB, Bachega TASS. Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency [Internet]. Clinics. 2011 ; 66( 8): 1361-1365.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/S1807-59322011000800009
Trabalho de evento-resumo periodico
Impact of Glucocorticoid Receptor Gene Polymorphisms on Lipid Profile of Children and Adolescents with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency (2011)
Moreira, R.; Gomes, L.; Madureira, G.; Mendonça, B.; Bachega, T.
Source: Hormone Research in Paediatrics. Conference titles: Annual Meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: POLIMORFISMO, CRIANÇAS, ADOLESCENTES, LIPÍDEOS, HIPERPLASIA SUPRARRENAL CONGÊNITA, HIDROXILASE (DEFICIÊNCIA), RESUMOS (EVENTOS)
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ABNT
MOREIRA, R. et al. Impact of Glucocorticoid Receptor Gene Polymorphisms on Lipid Profile of Children and Adolescents with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf. Acesso em: 20 fev. 2026. , 2011
APA
Moreira, R., Gomes, L., Madureira, G., Mendonça, B., & Bachega, T. (2011). Impact of Glucocorticoid Receptor Gene Polymorphisms on Lipid Profile of Children and Adolescents with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
NLM
Moreira R, Gomes L, Madureira G, Mendonça B, Bachega T. Impact of Glucocorticoid Receptor Gene Polymorphisms on Lipid Profile of Children and Adolescents with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 13 res. 34.[citado 2026 fev. 20 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
Vancouver
Moreira R, Gomes L, Madureira G, Mendonça B, Bachega T. Impact of Glucocorticoid Receptor Gene Polymorphisms on Lipid Profile of Children and Adolescents with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 13 res. 34.[citado 2026 fev. 20 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
Artigo de periodico
Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia (2011)
Hayashi, Giselle; Faure, Cláudia; Brondi, Maria Fernanda; Vallejos, Carla; Soares, Daiana; Oliveira, Érica; Brito, Vinícius N.; Mendonca, Berenice B.; Bachega, Tânia A. S. S.
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Unidade: FM
Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA, HIDROXILASE (DEFICIÊNCIA), RASTREAMENTO, RECÉM-NASCIDO, PROGESTERONA (NÍVEL;ANÁLISE)
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ABNT
HAYASHI, Giselle et al. Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 55, n. 8, p. 632-637, 2011Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302011000800019. Acesso em: 20 fev. 2026.
APA
Hayashi, G., Faure, C., Brondi, M. F., Vallejos, C., Soares, D., Oliveira, É., et al. (2011). Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia. Arquivos Brasileiros de Endocrinologia e Metabologia, 55( 8), 632-637. doi:10.1590/s0004-27302011000800019
NLM
Hayashi G, Faure C, Brondi MF, Vallejos C, Soares D, Oliveira É, Brito VN, Mendonca BB, Bachega TASS. Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2011 ; 55( 8): 632-637.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/s0004-27302011000800019
Vancouver
Hayashi G, Faure C, Brondi MF, Vallejos C, Soares D, Oliveira É, Brito VN, Mendonca BB, Bachega TASS. Weight-adjusted neonatal 17OH-progesterone cutoff levels improve the efficiency of newborn screening for congenital adrenal hyperplasia [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2011 ; 55( 8): 632-637.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/s0004-27302011000800019
Trabalho de evento-resumo periodico
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 (2010)
Moreira, R. P. P.; Brito, V. N.; Gomes, L. G.; Madureira, G.; Mendonça, B. B.; Bachega, T. A. S. S.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP). Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), SEGUIMENTOS, METABOLISMO BASAL (PATOLOGIA), CORTISOL (ANÁLISE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, R. P. P. et al. 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. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf. Acesso em: 20 fev. 2026. , 2010
APA
Moreira, R. P. P., Brito, V. N., Gomes, L. G., Madureira, G., Mendonça, B. B., & Bachega, T. A. S. S. (2010). 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. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
NLM
Moreira RPP, Brito VN, Gomes LG, Madureira G, Mendonça BB, Bachega TASS. 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 [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 12.[citado 2026 fev. 20 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Vancouver
Moreira RPP, Brito VN, Gomes LG, Madureira G, Mendonça BB, Bachega TASS. 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 [Internet]. Hormone Research in Paediatrics. 2010 ; 74( suppl. 1): 12.[citado 2026 fev. 20 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=320138&Ausgabe=254526&ProduktNr=224036&filename=320138.pdf
Artigo de periodico
Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency (2010)
Barbosa, Flávia A. Costa; Fernandes, Vânia F. Tonetto; Carvalho, valdemir M.; Nakamura, Odete H.; Moura, Vivian; Vieira, José G. H.; Bachega, Tânia A. S. S.; Kater, Claudio E.
Source: Clinical Endocrinology. Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), HIPERPLASIA SUPRARRENAL CONGÊNITA, SENSIBILIDADE E ESPECIFICIDADE, MENOPAUSA, BIOLOGIA MOLECULAR, GENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, Flávia A. Costa et al. Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency. Clinical Endocrinology, v. 73, n. 6, p. 700-706, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2010.03871.x. Acesso em: 20 fev. 2026.
APA
Barbosa, F. A. C., Fernandes, V. F. T., Carvalho, valdemir M., Nakamura, O. H., Moura, V., Vieira, J. G. H., et al. (2010). Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency. Clinical Endocrinology, 73( 6), 700-706. doi:10.1111/j.1365-2265.2010.03871.x
NLM
Barbosa FAC, Fernandes VFT, Carvalho valdemir M, Nakamura OH, Moura V, Vieira JGH, Bachega TASS, Kater CE. Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency [Internet]. Clinical Endocrinology. 2010 ; 73( 6): 700-706.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1111/j.1365-2265.2010.03871.x
Vancouver
Barbosa FAC, Fernandes VFT, Carvalho valdemir M, Nakamura OH, Moura V, Vieira JGH, Bachega TASS, Kater CE. Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency [Internet]. Clinical Endocrinology. 2010 ; 73( 6): 700-706.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1111/j.1365-2265.2010.03871.x
Trabalho de evento-resumo periodico
The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene (2010)
Moura, V O; Pacheco, M; Kaupert, L; Gomes, L G; Marcondes, J A M; Mendonça, Berenice Bilharinho de; Bachega, Tânia Aparecida Sartori Sanchez
Source: Clinics. Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP". Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), POLIMORFISMO, ANDRÓGENOS, RECEPTORES, GENES (ANÁLISE), RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOURA, V O et al. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 20 fev. 2026. , 2010
APA
Moura, V. O., Pacheco, M., Kaupert, L., Gomes, L. G., Marcondes, J. A. M., Mendonça, B. B. de, & Bachega, T. A. S. S. (2010). The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Moura VO, Pacheco M, Kaupert L, Gomes LG, Marcondes JAM, Mendonça BB de, Bachega TASS. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. 2010 ; 65 S70.[citado 2026 fev. 20 ]
Vancouver
Moura VO, Pacheco M, Kaupert L, Gomes LG, Marcondes JAM, Mendonça BB de, Bachega TASS. The presence of clitoomegaly in nonclassical form of 21-hydroxylase deficiency is modulated by the cag polymorphic tract of androgen receptor gene. Clinics. 2010 ; 65 S70.[citado 2026 fev. 20 ]
Trabalho de evento-resumo periodico
Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (2010)
Moreira, R P P; Kaupert, L C; Gomes, L G; Madureira, G; Mendonça, Berenice Bilharinho de; Bachega, Tânia Aparecida Sartori Sanchez
Source: Clinics. Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP". Unidade: FM
Subjects: FARMACOGENÉTICA, HIPERPLASIA SUPRARRENAL CONGÊNITA, HIDROXILASE (DEFICIÊNCIA), RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, R P P et al. Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 20 fev. 2026. , 2010
APA
Moreira, R. P. P., Kaupert, L. C., Gomes, L. G., Madureira, G., Mendonça, B. B. de, & Bachega, T. A. S. S. (2010). Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Moreira RPP, Kaupert LC, Gomes LG, Madureira G, Mendonça BB de, Bachega TASS. Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics. 2010 ; 65 S70.[citado 2026 fev. 20 ]
Vancouver
Moreira RPP, Kaupert LC, Gomes LG, Madureira G, Mendonça BB de, Bachega TASS. Pharmacogenetics optimizes the glucocorticoid replacement of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clinics. 2010 ; 65 S70.[citado 2026 fev. 20 ]
Trabalho de evento-resumo periodico
Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? (2010)
Moura, V O; Pacheco, M; Madureira, G; Marcondes, J A M; Mendonça, Berenice Bilharinho de; Bachega, Tânia Aparecida Sartori Sanchez
Source: Clinics. Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP". Unidade: FM
Subjects: FENÓTIPOS (VARIABILIDADE), HIDROXILASE (DEFICIÊNCIA), ALELOPATIA, GENÓTIPOS (VARIABILIDADE), TRANSTORNOS DA MENSTRUAÇÃO, PUBERDADE PRECOCE, RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOURA, V O et al. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency?. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 20 fev. 2026. , 2010
APA
Moura, V. O., Pacheco, M., Madureira, G., Marcondes, J. A. M., Mendonça, B. B. de, & Bachega, T. A. S. S. (2010). Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
NLM
Moura VO, Pacheco M, Madureira G, Marcondes JAM, Mendonça BB de, Bachega TASS. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. 2010 ; 65 S70.[citado 2026 fev. 20 ]
Vancouver
Moura VO, Pacheco M, Madureira G, Marcondes JAM, Mendonça BB de, Bachega TASS. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. 2010 ; 65 S70.[citado 2026 fev. 20 ]
Artigo de periodico
Giant adrenal myelolipoma associated with 21-hydroxylase deficiency: unusual association mimicking an androgen-secreting adrenocortical carcinoma (2010)
Mermejo, Lívia Mara; Elias Júnior, Jorge; Saggioro, Fabiano Pinto; Tucci Júnior, Silvio; Castro, Margaret de; Moreira, Ayrton Custódio; Elias, Paula Conde Lamparelli
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Unidade: FMRP
Subjects: CARCINOMA (DIAGNÓSTICO), HIDROXILASE (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MERMEJO, Lívia Mara et al. Giant adrenal myelolipoma associated with 21-hydroxylase deficiency: unusual association mimicking an androgen-secreting adrenocortical carcinoma. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 54, n. 4, p. 419-424, 2010Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302010000400012. Acesso em: 20 fev. 2026.
APA
Mermejo, L. M., Elias Júnior, J., Saggioro, F. P., Tucci Júnior, S., Castro, M. de, Moreira, A. C., & Elias, P. C. L. (2010). Giant adrenal myelolipoma associated with 21-hydroxylase deficiency: unusual association mimicking an androgen-secreting adrenocortical carcinoma. Arquivos Brasileiros de Endocrinologia e Metabologia, 54( 4), 419-424. doi:10.1590/s0004-27302010000400012
NLM
Mermejo LM, Elias Júnior J, Saggioro FP, Tucci Júnior S, Castro M de, Moreira AC, Elias PCL. Giant adrenal myelolipoma associated with 21-hydroxylase deficiency: unusual association mimicking an androgen-secreting adrenocortical carcinoma [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2010 ; 54( 4): 419-424.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/s0004-27302010000400012
Vancouver
Mermejo LM, Elias Júnior J, Saggioro FP, Tucci Júnior S, Castro M de, Moreira AC, Elias PCL. Giant adrenal myelolipoma associated with 21-hydroxylase deficiency: unusual association mimicking an androgen-secreting adrenocortical carcinoma [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2010 ; 54( 4): 419-424.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/s0004-27302010000400012
Artigo de periodico
Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency (2009)
Gomes, Larissa G.
Source: The journal clinical endocrinology & metabolism. Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), MUTAÇÃO GENÉTICA, FENÓTIPOS, ENZIMAS (ANÁLISE), BIOENSAIOS, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Larissa G. Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency. The journal clinical endocrinology & metabolism, v. 94, n. 1, p. 89-95, 2009Tradução . . Disponível em: https://doi.org/10.1210/jc.2008-1174. Acesso em: 20 fev. 2026.
APA
Gomes, L. G. (2009). Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency. The journal clinical endocrinology & metabolism, 94( 1), 89-95. doi:10.1210/jc.2008-1174
NLM
Gomes LG. Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency [Internet]. The journal clinical endocrinology & metabolism. 2009 ; 94( 1): 89-95.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1210/jc.2008-1174
Vancouver
Gomes LG. Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency [Internet]. The journal clinical endocrinology & metabolism. 2009 ; 94( 1): 89-95.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1210/jc.2008-1174
Artigo de periodico
Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients (2009)
Soardi, Fernanda C.; Penachioni, Junia Y.; Justo, Giselle Z.; Bachega, Tânia A. S. S.; Inácio, Marlene; Mendonça, Berenice Bilharinho de; Castro, Margaret de; Mello, Maricilda P. de
Source: Journal of clinical endocrinology and metabolism. Unidades: FM, FMRP
Subjects: HIDROXILASE (DEFICIÊNCIA), GENES (CLASSIFICAÇÃO), MUTAÇÃO GENÉTICA, FENÓTIPOS, HIPERTENSÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOARDI, Fernanda C. et al. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism, v. 94, n. 9, p. 3481-3485, 2009Tradução . . Acesso em: 20 fev. 2026.
APA
Soardi, F. C., Penachioni, J. Y., Justo, G. Z., Bachega, T. A. S. S., Inácio, M., Mendonça, B. B. de, et al. (2009). Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism, 94( 9), 3481-3485.
NLM
Soardi FC, Penachioni JY, Justo GZ, Bachega TASS, Inácio M, Mendonça BB de, Castro M de, Mello MP de. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism. 2009 ; 94( 9): 3481-3485.[citado 2026 fev. 20 ]
Vancouver
Soardi FC, Penachioni JY, Justo GZ, Bachega TASS, Inácio M, Mendonça BB de, Castro M de, Mello MP de. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism. 2009 ; 94( 9): 3481-3485.[citado 2026 fev. 20 ]
Artigo de periodico
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 (2008)
Martin, Regina M.; Oliveira, Paulo S.; Costa, Elaine M. F.; Arnhold, Ivo J. P.; Mendonça, Berenice Bilharinho de
Source: Arquivos brasileiros de endocrinologia e metabologia. Unidade: FM
Subjects: HIDROXILASE (DEFICIÊNCIA), HIPERTENSÃO, HIPERPLASIA SUPRARRENAL CONGÊNITA, PROGESTERONA, MODELAGEM MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTIN, Regina M. et al. 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. Arquivos brasileiros de endocrinologia e metabologia, v. 52, n. 8, p. 1317-1320, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302008000800018. Acesso em: 20 fev. 2026.
APA
Martin, R. M., Oliveira, P. S., Costa, E. M. F., Arnhold, I. J. P., & Mendonça, B. B. de. (2008). 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. Arquivos brasileiros de endocrinologia e metabologia, 52( 8), 1317-1320. doi:10.1590/s0004-27302008000800018
NLM
Martin RM, Oliveira PS, Costa EMF, Arnhold IJP, Mendonça BB de. 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 [Internet]. Arquivos brasileiros de endocrinologia e metabologia. 2008 ; 52( 8): 1317-1320.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/s0004-27302008000800018
Vancouver
Martin RM, Oliveira PS, Costa EMF, Arnhold IJP, Mendonça BB de. 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 [Internet]. Arquivos brasileiros de endocrinologia e metabologia. 2008 ; 52( 8): 1317-1320.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1590/s0004-27302008000800018
Artigo de periodico
The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene (2008)
Rocha, Rosana O.; Billerbeck, Ana Elisa C.; Pinto, Emília M.; Melo, Karla F. S.; Lin, Chin J.; Longui, Carlos A.; Mendonca, Berenice B.; Bachega, Tânia A. S. S.
Source: Clinical Endocrinology. Unidade: FM
Subjects: GENITÁLIA FEMININA, ADOLESCENTES, FENÓTIPOS, HIDROXILASE (DEFICIÊNCIA), RECEPTORES ANDROGÊNICOS, CONFERÊNCIA INTERNACIONAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROCHA, Rosana O. et al. The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene. Clinical Endocrinology, v. 68, n. 2, p. 226-232, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.03023.x. Acesso em: 20 fev. 2026.
APA
Rocha, R. O., Billerbeck, A. E. C., Pinto, E. M., Melo, K. F. S., Lin, C. J., Longui, C. A., et al. (2008). The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene. Clinical Endocrinology, 68( 2), 226-232. doi:10.1111/j.1365-2265.2007.03023.x
NLM
Rocha RO, Billerbeck AEC, Pinto EM, Melo KFS, Lin CJ, Longui CA, Mendonca BB, Bachega TASS. The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene [Internet]. Clinical Endocrinology. 2008 ; 68( 2): 226-232.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03023.x
Vancouver
Rocha RO, Billerbeck AEC, Pinto EM, Melo KFS, Lin CJ, Longui CA, Mendonca BB, Bachega TASS. The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene [Internet]. Clinical Endocrinology. 2008 ; 68( 2): 226-232.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03023.x
Artigo de periodico
The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency (2008)
Gomes, Larissa G.; Huang, Ningwu; Mendonça, Berenice B.; Bachega, Tania A. S. S.; Miller, Walter L.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: ENZIMAS OXIRREDUTORAS (VACINAÇÃO), HIDROXILASE (DEFICIÊNCIA), FENÓTIPOS, GENÓTIPOS, POLIMORFISMO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Larissa G. et al. The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency. Journal of Clinical Endocrinology and Metabolism, v. 93, n. 7, p. 2913-2916, 2008Tradução . . Disponível em: https://doi.org/10.1210/jc.2008-0304. Acesso em: 20 fev. 2026.
APA
Gomes, L. G., Huang, N., Mendonça, B. B., Bachega, T. A. S. S., & Miller, W. L. (2008). The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency. Journal of Clinical Endocrinology and Metabolism, 93( 7), 2913-2916. doi:10.1210/jc.2008-0304
NLM
Gomes LG, Huang N, Mendonça BB, Bachega TASS, Miller WL. The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 7): 2913-2916.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1210/jc.2008-0304
Vancouver
Gomes LG, Huang N, Mendonça BB, Bachega TASS, Miller WL. The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 7): 2913-2916.[citado 2026 fev. 20 ] Available from: https://doi.org/10.1210/jc.2008-0304

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