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Artigo de periodico
Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor (2018)
Batista, Rafael Loch; Rodrigues, Andresa De Santi; Machado, Aline Zamboni; Nishi, Mirian; Cunha, Flavia Siqueira; Silva, Rosana Barbosa; Costa, Elaine M. F.; Mendonça, Berenice Bilharinho de; Domenice, Sorahia
Source: Journal of pediatric endocrinology & metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, ANDRÓGENOS, RECEPTORES ANDROGÊNICOS
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ABNT
BATISTA, Rafael Loch et al. Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor. Journal of pediatric endocrinology & metabolism, v. 31, n. 2, p. 223-228, 2018Tradução . . Disponível em: https://doi.org/10.1515/jpem-2017-0095. Acesso em: 20 ago. 2024.
APA
Batista, R. L., Rodrigues, A. D. S., Machado, A. Z., Nishi, M., Cunha, F. S., Silva, R. B., et al. (2018). Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor. Journal of pediatric endocrinology & metabolism, 31( 2), 223-228. doi:10.1515/jpem-2017-0095
NLM
Batista RL, Rodrigues ADS, Machado AZ, Nishi M, Cunha FS, Silva RB, Costa EMF, Mendonça BB de, Domenice S. Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor [Internet]. Journal of pediatric endocrinology & metabolism. 2018 ; 31( 2): 223-228.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1515/jpem-2017-0095
Vancouver
Batista RL, Rodrigues ADS, Machado AZ, Nishi M, Cunha FS, Silva RB, Costa EMF, Mendonça BB de, Domenice S. Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor [Internet]. Journal of pediatric endocrinology & metabolism. 2018 ; 31( 2): 223-228.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1515/jpem-2017-0095
Artigo de periodico
46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency (2017)
Mendonça, Berenice B.; Gomes, Nathalia Lisboa; Domenice, Sorahia; Costa, Elaine M. F.; Inacio, Marlene; Martin, Regina M.; Nishi, Mirian Y.; Carvalho, Filomena Marino; Tibor, Francisco Denes
Source: The Journal of Steroid Biochemistry and Molecular Biology. Unidade: FM
Subjects: TRANSTORNOS DA DIFERENCIAÇÃO SEXUAL, TESTOSTERONA, GENITÁLIA, CARCINOGÊNESE
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ABNT
MENDONÇA, Berenice B. et al. 46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency. The Journal of Steroid Biochemistry and Molecular Biology, v. 165, p. 79-85, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jsbmb.2016.05.002. Acesso em: 20 ago. 2024.
APA
Mendonça, B. B., Gomes, N. L., Domenice, S., Costa, E. M. F., Inacio, M., Martin, R. M., et al. (2017). 46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency. The Journal of Steroid Biochemistry and Molecular Biology, 165, 79-85. doi:10.1016/j.jsbmb.2016.05.002
NLM
Mendonça BB, Gomes NL, Domenice S, Costa EMF, Inacio M, Martin RM, Nishi MY, Carvalho FM, Tibor FD. 46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency [Internet]. The Journal of Steroid Biochemistry and Molecular Biology. 2017 ; 165 79-85.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.jsbmb.2016.05.002
Vancouver
Mendonça BB, Gomes NL, Domenice S, Costa EMF, Inacio M, Martin RM, Nishi MY, Carvalho FM, Tibor FD. 46,XY disorder of sex development (DSD) due to 17b-hydroxysteroid dehydrogenase type 3 deficiency [Internet]. The Journal of Steroid Biochemistry and Molecular Biology. 2017 ; 165 79-85.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.jsbmb.2016.05.002
Artigo de periodico
Reprint of “Steroid 5-reductase 2 deficiency” (2017)
Mendonça, Berenice B.; Batista, Rafael Loch; Domenice, Sorahia; Costa, Elaine M. F.; Arnhold, Ivo J.; Russell, David W.; Wilson, Jean D.
Source: The Journal of Steroid Biochemistry and Molecular Biology. Unidade: FM
Subjects: ENZIMAS, TESTOSTERONA, GENITÁLIA, DIFERENÇAS SEXUAIS (PSICOGÊNESE), TRANSTORNOS DA DIFERENCIAÇÃO SEXUAL
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ABNT
MENDONÇA, Berenice B. et al. Reprint of “Steroid 5-reductase 2 deficiency”. The Journal of Steroid Biochemistry and Molecular Biology, v. 165, p. 95-100, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jsbmb.2016.11.006. Acesso em: 20 ago. 2024.
APA
Mendonça, B. B., Batista, R. L., Domenice, S., Costa, E. M. F., Arnhold, I. J., Russell, D. W., & Wilson, J. D. (2017). Reprint of “Steroid 5-reductase 2 deficiency”. The Journal of Steroid Biochemistry and Molecular Biology, 165, 95-100. doi:10.1016/j.jsbmb.2016.11.006
NLM
Mendonça BB, Batista RL, Domenice S, Costa EMF, Arnhold IJ, Russell DW, Wilson JD. Reprint of “Steroid 5-reductase 2 deficiency” [Internet]. The Journal of Steroid Biochemistry and Molecular Biology. 2017 ; 165 95-100.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.jsbmb.2016.11.006
Vancouver
Mendonça BB, Batista RL, Domenice S, Costa EMF, Arnhold IJ, Russell DW, Wilson JD. Reprint of “Steroid 5-reductase 2 deficiency” [Internet]. The Journal of Steroid Biochemistry and Molecular Biology. 2017 ; 165 95-100.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.jsbmb.2016.11.006
Artigo de periodico
The clinical structural and biological features of neovaginas: A comparison of the Frank and the McIndoe techniques (2015)
Hayashida, Sylvia A.; Soares Junior, Jose Maria; Costa, Elaine M. F.; Fonseca, Angela M. da; Maciel, Gustavo A. R.; Mendonça, Berenice B.; Baracat, Edmund C.
Source: European Journal of Obstetrics & Gynecology and Reproductive Biology. Unidade: FM
Subjects: GENITÁLIA FEMININA (CIRURGIA), VAGINA, PROCEDIMENTOS CIRÚRGICOS EM GINECOLOGIA
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ABNT
HAYASHIDA, Sylvia A. et al. The clinical structural and biological features of neovaginas: A comparison of the Frank and the McIndoe techniques. European Journal of Obstetrics & Gynecology and Reproductive Biology, v. 186, p. 12-16, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ejogrb.2014.12.025. Acesso em: 20 ago. 2024.
APA
Hayashida, S. A., Soares Junior, J. M., Costa, E. M. F., Fonseca, A. M. da, Maciel, G. A. R., Mendonça, B. B., & Baracat, E. C. (2015). The clinical structural and biological features of neovaginas: A comparison of the Frank and the McIndoe techniques. European Journal of Obstetrics & Gynecology and Reproductive Biology, 186, 12-16. doi:10.1016/j.ejogrb.2014.12.025
NLM
Hayashida SA, Soares Junior JM, Costa EMF, Fonseca AM da, Maciel GAR, Mendonça BB, Baracat EC. The clinical structural and biological features of neovaginas: A comparison of the Frank and the McIndoe techniques [Internet]. European Journal of Obstetrics & Gynecology and Reproductive Biology. 2015 ; 186 12-16.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.ejogrb.2014.12.025
Vancouver
Hayashida SA, Soares Junior JM, Costa EMF, Fonseca AM da, Maciel GAR, Mendonça BB, Baracat EC. The clinical structural and biological features of neovaginas: A comparison of the Frank and the McIndoe techniques [Internet]. European Journal of Obstetrics & Gynecology and Reproductive Biology. 2015 ; 186 12-16.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.ejogrb.2014.12.025
Artigo de periodico
Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay (2014)
Beneduzzi, Daiane; Trarbach, Ericka B.; Min, Le; Jorge, Alexander A. L.; Garmes, Heraldo M.; Renk, Alessandra Covallero; Fichna, Marta; Fichna, Piotr; Arantes, Karina A.; Costa, Elaine M. F.; Zhang, Anna; Adeola, Oluwaseun; Wen, Junping; Carroll, Rona S.; Mendonça, Berenice B.; Kaiser, Ursula B.; Latronico, , Ana Claudia; Silveira, Letícia F. G.
Source: Fertility and Sterility. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, PUBERDADE, HIPOGONADISMO
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ABNT
BENEDUZZI, Daiane et al. Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay. Fertility and Sterility, v. 102, n. 3, p. 838-846, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.fertnstert.2014.05.044. Acesso em: 20 ago. 2024.
APA
Beneduzzi, D., Trarbach, E. B., Min, L., Jorge, A. A. L., Garmes, H. M., Renk, A. C., et al. (2014). Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay. Fertility and Sterility, 102( 3), 838-846. doi:10.1016/j.fertnstert.2014.05.044
NLM
Beneduzzi D, Trarbach EB, Min L, Jorge AAL, Garmes HM, Renk AC, Fichna M, Fichna P, Arantes KA, Costa EMF, Zhang A, Adeola O, Wen J, Carroll RS, Mendonça BB, Kaiser UB, Latronico, Silveira LFG. Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay [Internet]. Fertility and Sterility. 2014 ; 102( 3): 838-846.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.fertnstert.2014.05.044
Vancouver
Beneduzzi D, Trarbach EB, Min L, Jorge AAL, Garmes HM, Renk AC, Fichna M, Fichna P, Arantes KA, Costa EMF, Zhang A, Adeola O, Wen J, Carroll RS, Mendonça BB, Kaiser UB, Latronico, Silveira LFG. Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay [Internet]. Fertility and Sterility. 2014 ; 102( 3): 838-846.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.fertnstert.2014.05.044
Artigo de periodico
Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency (2014)
Santos, Mariza G.; Machado, Aline Z.; Martins, Conceição N.; Domenice, Sorahia; Mendonça, Berenice B.; Costa, Elaine M. F.; Nishi, Mirian Y.; Ferraz-de-Souza, Bruno; Jorge, Soraia A. C.; Pereira, Carlos A.; Soardi, Fernanda c.; Mello, Maricilda P. de; Maciel-Guerra, Andrea T.; Guerra Junior, Gil
Source: BioMed Research International. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, OVÁRIO (ANORMALIDADES), APOPTOSE
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ABNT
SANTOS, Mariza G. et al. Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency. BioMed Research International, v. 2014, p. 8 art, 2014Tradução . . Disponível em: https://doi.org/10.1155/2014/787465. Acesso em: 20 ago. 2024.
APA
Santos, M. G., Machado, A. Z., Martins, C. N., Domenice, S., Mendonça, B. B., Costa, E. M. F., et al. (2014). Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency. BioMed Research International, 2014, 8 art. doi:10.1155/2014/787465
NLM
Santos MG, Machado AZ, Martins CN, Domenice S, Mendonça BB, Costa EMF, Nishi MY, Ferraz-de-Souza B, Jorge SAC, Pereira CA, Soardi F c., Mello MP de, Maciel-Guerra AT, Guerra Junior G. Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency [Internet]. BioMed Research International. 2014 ; 2014 8 art.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1155/2014/787465
Vancouver
Santos MG, Machado AZ, Martins CN, Domenice S, Mendonça BB, Costa EMF, Nishi MY, Ferraz-de-Souza B, Jorge SAC, Pereira CA, Soardi F c., Mello MP de, Maciel-Guerra AT, Guerra Junior G. Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency [Internet]. BioMed Research International. 2014 ; 2014 8 art.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1155/2014/787465
Trabalho de evento-resumo periodico
Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia (2013)
Fanelli, Marina; Silva, Rosana B. Silva; Domenice, Sorahia.; Mendonça, Berenice Bilharinho de; Costa, Elaine M. F.
Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Subjects: GENES (ANÁLISE), TRANSTORNOS GONADAIS, ENDOCRINOPATIAS
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ABNT
FANELLI, Marina et al. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 20 ago. 2024. , 2013
APA
Fanelli, M., Silva, R. B. S., Domenice, S., Mendonça, B. B. de, & Costa, E. M. F. (2013). Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Fanelli M, Silva RBS, Domenice S, Mendonça BB de, Costa EMF. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80 185.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Fanelli M, Silva RBS, Domenice S, Mendonça BB de, Costa EMF. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80 185.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1159/000353762
Artigo de periodico
Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age (2013)
Coletta, Rocio R. D.; Jorge, Alexander A. L.; D'Alva, Catarina Brasil; Pinto, Emília M.; Billerbeck, Ana Elisa C.; Pachi, Paulo R.; Longui, Carlos A.; Garcia, Ricardo M.; Boguszewski, Margaret; Arnhold, Ivo J. P.; Mendonca, Berenice B.; Costa, Elaine M. F.
Source: Clinics. Unidade: FM
Subjects: IDADE GESTACIONAL, FATORES DE CRESCIMENTO, INSULINA, RECÉM-NASCIDO PEQUENO PARA IDADE GESTACIONAL, GENÓTIPOS, REAÇÃO EM CADEIA POR POLIMERASE, POLIMORFISMO
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ABNT
COLETTA, Rocio R. D. et al. Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age. Clinics, v. 68, n. 6, p. 785-791, 2013Tradução . . Disponível em: https://doi.org/10.6061/clinics/2013(06)10. Acesso em: 20 ago. 2024.
APA
Coletta, R. R. D., Jorge, A. A. L., D'Alva, C. B., Pinto, E. M., Billerbeck, A. E. C., Pachi, P. R., et al. (2013). Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age. Clinics, 68( 6), 785-791. doi:10.6061/clinics/2013(06)10
NLM
Coletta RRD, Jorge AAL, D'Alva CB, Pinto EM, Billerbeck AEC, Pachi PR, Longui CA, Garcia RM, Boguszewski M, Arnhold IJP, Mendonca BB, Costa EMF. Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age [Internet]. Clinics. 2013 ; 68( 6): 785-791.[citado 2024 ago. 20 ] Available from: https://doi.org/10.6061/clinics/2013(06)10
Vancouver
Coletta RRD, Jorge AAL, D'Alva CB, Pinto EM, Billerbeck AEC, Pachi PR, Longui CA, Garcia RM, Boguszewski M, Arnhold IJP, Mendonca BB, Costa EMF. Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age [Internet]. Clinics. 2013 ; 68( 6): 785-791.[citado 2024 ago. 20 ] Available from: https://doi.org/10.6061/clinics/2013(06)10
Trabalho de evento-resumo periodico
Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations (2012)
Beneduzzi, Daiane; Costa, Elaine M. F.; Abreu, Ana Paula; Lofrano-Porto, Adriana; Silveira, Leticia G. F.; Mendonça, Berenice B.; Trarbach, Ericka B.; Latronico, Ana Claudia
Source: Hormone research in paediatrics. Conference titles: 51th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Unidade: FM
Subjects: GENÓTIPOS, RECEPTORES HORMONAIS, GONADOTROFINAS HIPOFISÁRIAS, FENÓTIPOS, HIPOGONADISMO, HORMÔNOS (USO TERAPÊUTICO), RESUMOS (EVENTOS)
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ABNT
BENEDUZZI, Daiane et al. Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000343181. Acesso em: 20 ago. 2024. , 2012
APA
Beneduzzi, D., Costa, E. M. F., Abreu, A. P., Lofrano-Porto, A., Silveira, L. G. F., Mendonça, B. B., et al. (2012). Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000343181
NLM
Beneduzzi D, Costa EMF, Abreu AP, Lofrano-Porto A, Silveira LGF, Mendonça BB, Trarbach EB, Latronico AC. Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 42.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1159/000343181
Vancouver
Beneduzzi D, Costa EMF, Abreu AP, Lofrano-Porto A, Silveira LGF, Mendonça BB, Trarbach EB, Latronico AC. Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 42.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1159/000343181
Artigo de periodico
Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations (2012)
Beneduzzi, Daiane; Costa, Elaine M. F.; Silveira, Leticia; Trarbach, Ericka; Abreu, Ana Paula; Porto, Adriana Lofrano; Latronico, Ana C.; Mendonca, Berenice B.
Source: Endocrine Reviews. Conference titles: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo. Unidade: FM
Subjects: GENÓTIPOS, MUTAÇÃO GENÉTICA, FENÓTIPOS, HIPOGONADISMO, RESUMOS (EVENTOS)
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ABNT
BENEDUZZI, Daiane et al. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618. Acesso em: 20 ago. 2024.
APA
Beneduzzi, D., Costa, E. M. F., Silveira, L., Trarbach, E., Abreu, A. P., Porto, A. L., et al. (2012). Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618
NLM
Beneduzzi D, Costa EMF, Silveira L, Trarbach E, Abreu AP, Porto AL, Latronico AC, Mendonca BB. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 ago. 20 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618
Vancouver
Beneduzzi D, Costa EMF, Silveira L, Trarbach E, Abreu AP, Porto AL, Latronico AC, Mendonca BB. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 ago. 20 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618
Trabalho de evento-resumo periodico
Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort (2011)
Silveira, Letícia F. G.; Teles, Milena G.; Abreu, Ana P.; Montenegro, Luciana Ribeiro; Tusset, Cíntia; Beneduzzi, Daiane; Castro, Margaret de; Costa, Elaine M. F.; Lofrano-Porto, Adriana; Baptista, Maria T. M.; Garmes, Heraldo M.; Guerra-Júnior, Gil; Mendonça, Berenice Bilharinho de; Latronico, Ana C.; Trarbach, Ericka B.
Source: Endocrine Reviews. Conference titles: International Pituitary Congress. Unidades: FMRP, FM
Assunto: ENDOCRINOLOGIA
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ABNT
SILVEIRA, Letícia F. G. et al. Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort. Endocrine Reviews. Chevy Chase: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 20 ago. 2024. , 2011
APA
Silveira, L. F. G., Teles, M. G., Abreu, A. P., Montenegro, L. R., Tusset, C., Beneduzzi, D., et al. (2011). Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort. Endocrine Reviews. Chevy Chase: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Silveira LFG, Teles MG, Abreu AP, Montenegro LR, Tusset C, Beneduzzi D, Castro M de, Costa EMF, Lofrano-Porto A, Baptista MTM, Garmes HM, Guerra-Júnior G, Mendonça BB de, Latronico AC, Trarbach EB. Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort. Endocrine Reviews. 2011 ; 32[citado 2024 ago. 20 ]
Vancouver
Silveira LFG, Teles MG, Abreu AP, Montenegro LR, Tusset C, Beneduzzi D, Castro M de, Costa EMF, Lofrano-Porto A, Baptista MTM, Garmes HM, Guerra-Júnior G, Mendonça BB de, Latronico AC, Trarbach EB. Congenital isolated hypogonadotropic hypogonadism: a detailed clinical and molecular characterization of a Brazilian patient cohort. Endocrine Reviews. 2011 ; 32[citado 2024 ago. 20 ]
Trabalho de evento-resumo periodico
Inactivating mutations in SF1 do not impair gonadotropin production in 46,XY patients with disorders of sex development (DSD) (2010)
Domenice, Sorahia; Santos, Mariza G.; Machado, Aline Z.; Hohl, Cecilia A.; Gadelha, Patricia Spara; Brandão, Maria P.; Correa, Rafaela V.; Lando, Valéria S.; Costa, Elaine M. F.; Mendonça, Berenice B.
Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the European Society for Pediatric Endocrinology (ESPE). Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GONADOTROFINAS (PRODUÇÃO;SECREÇÃO), DISTÚRBIOS DA FUNÇÃO SEXUAL, RESUMOS (EVENTOS)
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ABNT
DOMENICE, Sorahia et al. Inactivating mutations in SF1 do not impair gonadotropin production in 46,XY patients with disorders of sex development (DSD). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 20 ago. 2024. , 2010
APA
Domenice, S., Santos, M. G., Machado, A. Z., Hohl, C. A., Gadelha, P. S., Brandão, M. P., et al. (2010). Inactivating mutations in SF1 do not impair gonadotropin production in 46,XY patients with disorders of sex development (DSD). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Domenice S, Santos MG, Machado AZ, Hohl CA, Gadelha PS, Brandão MP, Correa RV, Lando VS, Costa EMF, Mendonça BB. Inactivating mutations in SF1 do not impair gonadotropin production in 46,XY patients with disorders of sex development (DSD). Hormone Research in Paediatrics. 2010 ; 74( suppl. 3): 207.[citado 2024 ago. 20 ]
Vancouver
Domenice S, Santos MG, Machado AZ, Hohl CA, Gadelha PS, Brandão MP, Correa RV, Lando VS, Costa EMF, Mendonça BB. Inactivating mutations in SF1 do not impair gonadotropin production in 46,XY patients with disorders of sex development (DSD). Hormone Research in Paediatrics. 2010 ; 74( suppl. 3): 207.[citado 2024 ago. 20 ]
Artigo de periodico
Long-Term Surgical Outcome of Masculinizing Genitoplasty in Large Cohort of Patients With Disorders of Sex Development (2010)
Sircili, Maria Helena Palma; Silva, Frederico Arnaldo de Queiroz e; Costa, Elaine M. F.; Brito, Vinicius N.; Arnhold, Ivo J. P.; Dénes, Francisco Tibor; Inacio, Marlene; Mendonça, Berenice Bilharinho de
Source: Journal of Urology. Unidade: FM
Subjects: GENITÁLIA MASCULINA, HOMENS, DIFERENCIAÇÃO SEXUAL (NÚCLEO CELULAR), SEGUIMENTOS, PROCEDIMENTOS CIRÚRGICOS UROLÓGICOS, PSEUDO-HERMAFRODITISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIRCILI, Maria Helena Palma et al. Long-Term Surgical Outcome of Masculinizing Genitoplasty in Large Cohort of Patients With Disorders of Sex Development. Journal of Urology, v. 184, n. 3, p. 1122-1127, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.jpurol.2010.02.172. Acesso em: 20 ago. 2024.
APA
Sircili, M. H. P., Silva, F. A. de Q. e, Costa, E. M. F., Brito, V. N., Arnhold, I. J. P., Dénes, F. T., et al. (2010). Long-Term Surgical Outcome of Masculinizing Genitoplasty in Large Cohort of Patients With Disorders of Sex Development. Journal of Urology, 184( 3), 1122-1127. doi:10.1016/j.jpurol.2010.02.172
NLM
Sircili MHP, Silva FA de Q e, Costa EMF, Brito VN, Arnhold IJP, Dénes FT, Inacio M, Mendonça BB de. Long-Term Surgical Outcome of Masculinizing Genitoplasty in Large Cohort of Patients With Disorders of Sex Development [Internet]. Journal of Urology. 2010 ; 184( 3): 1122-1127.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.jpurol.2010.02.172
Vancouver
Sircili MHP, Silva FA de Q e, Costa EMF, Brito VN, Arnhold IJP, Dénes FT, Inacio M, Mendonça BB de. Long-Term Surgical Outcome of Masculinizing Genitoplasty in Large Cohort of Patients With Disorders of Sex Development [Internet]. Journal of Urology. 2010 ; 184( 3): 1122-1127.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.jpurol.2010.02.172
Artigo de periodico
46,XY DSD due to impaired androgen production (2010)
Mendonça, Berenice B.; Costa, Elaine M. F.; Belgorosky, Alicia; Rivarola, Marco Aurelio; Domenice, Sorahia
Source: Best Practice & Research Clinical Endocrinology & Metabolism. Unidade: IAG
Subjects: ANDRÓGENOS (PRODUÇÃO), TESTOSTERONA (BIOSSÍNTESE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MENDONÇA, Berenice B. et al. 46,XY DSD due to impaired androgen production. Best Practice & Research Clinical Endocrinology & Metabolism, v. 24, n. 2, p. 243-262, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.beem.2009.11.003. Acesso em: 20 ago. 2024.
APA
Mendonça, B. B., Costa, E. M. F., Belgorosky, A., Rivarola, M. A., & Domenice, S. (2010). 46,XY DSD due to impaired androgen production. Best Practice & Research Clinical Endocrinology & Metabolism, 24( 2), 243-262. doi:10.1016/j.beem.2009.11.003
NLM
Mendonça BB, Costa EMF, Belgorosky A, Rivarola MA, Domenice S. 46,XY DSD due to impaired androgen production [Internet]. Best Practice & Research Clinical Endocrinology & Metabolism. 2010 ; 24( 2): 243-262.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.beem.2009.11.003
Vancouver
Mendonça BB, Costa EMF, Belgorosky A, Rivarola MA, Domenice S. 46,XY DSD due to impaired androgen production [Internet]. Best Practice & Research Clinical Endocrinology & Metabolism. 2010 ; 24( 2): 243-262.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.beem.2009.11.003
Artigo de periodico
46,XY disorders of sex developement (DSD) (2009)
Mendonça, Berenice Bilharinho; Domenice, Sorahia; Arnhold, Ivo J. P.; Costa, Elaine M. F.
Source: Clinical endocrinology. Unidade: FM
Subjects: TRANSTORNOS GONADAIS, DESENVOLVIMENTO PSICOSSOCIAL, TRANSTORNOS DA DIFERENCIAÇÃO SEXUAL (CONGÊNITO), FENÓTIPOS, PSEUDO-HERMAFRODITISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MENDONÇA, Berenice Bilharinho et al. 46,XY disorders of sex developement (DSD). Clinical endocrinology, v. 70, n. 2, p. 173-187, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.02993.x-i1. Acesso em: 20 ago. 2024.
APA
Mendonça, B. B., Domenice, S., Arnhold, I. J. P., & Costa, E. M. F. (2009). 46,XY disorders of sex developement (DSD). Clinical endocrinology, 70( 2), 173-187. doi:10.1111/j.1365-2265.2007.02993.x-i1
NLM
Mendonça BB, Domenice S, Arnhold IJP, Costa EMF. 46,XY disorders of sex developement (DSD) [Internet]. Clinical endocrinology. 2009 ; 70( 2): 173-187.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02993.x-i1
Vancouver
Mendonça BB, Domenice S, Arnhold IJP, Costa EMF. 46,XY disorders of sex developement (DSD) [Internet]. Clinical endocrinology. 2009 ; 70( 2): 173-187.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.02993.x-i1
Trabalho de evento-resumo periodico
Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development (2008)
Santos, Mariza A. G.; Nishi, Mirian Y.; Gomes, Camila; Domenice, Sorahia; Mendonça, Berenice B.; Costa, Elaine M. F.
Source: Hormone Research. Conference titles: European Society for Paediatric Endocrinology (ESPE). Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, TRANSTORNOS GONADAIS, RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Mariza A. G. et al. Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development. Hormone Research. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 20 ago. 2024. , 2008
APA
Santos, M. A. G., Nishi, M. Y., Gomes, C., Domenice, S., Mendonça, B. B., & Costa, E. M. F. (2008). Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development. Hormone Research. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Santos MAG, Nishi MY, Gomes C, Domenice S, Mendonça BB, Costa EMF. Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development. Hormone Research. 2008 ; 70 193.[citado 2024 ago. 20 ]
Vancouver
Santos MAG, Nishi MY, Gomes C, Domenice S, Mendonça BB, Costa EMF. Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development. Hormone Research. 2008 ; 70 193.[citado 2024 ago. 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 ago. 2024.
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 2024 ago. 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 2024 ago. 20 ] Available from: https://doi.org/10.1590/s0004-27302008000800018
Trabalho de evento-resumo periodico
A complex submicroscopic chromosomal imbalance in Xp 21,2 with microduplication and one microtriplication containing the DAX1 gene in a patient with 46,XY/47,XY,+markaryotype with partial gonadal dysgenesis and gonadoblastoma (2008)
Costa, Elaine M. F.; Nishi, Mirian Y.; Pinto, Emilia M.; Domenice, Sorahia; Mendonça, Berenice B.
Source: Hormone Research. Conference titles: European Society for Paediatric Endocrinology (ESPE). Unidade: FM
Subjects: CROMOSSOMOS, TRANSTORNOS GONADAIS, RESUMOS (EVENTOS)
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ABNT
COSTA, Elaine M. F. et al. A complex submicroscopic chromosomal imbalance in Xp 21,2 with microduplication and one microtriplication containing the DAX1 gene in a patient with 46,XY/47,XY,+markaryotype with partial gonadal dysgenesis and gonadoblastoma. Hormone Research. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 20 ago. 2024. , 2008
APA
Costa, E. M. F., Nishi, M. Y., Pinto, E. M., Domenice, S., & Mendonça, B. B. (2008). A complex submicroscopic chromosomal imbalance in Xp 21,2 with microduplication and one microtriplication containing the DAX1 gene in a patient with 46,XY/47,XY,+markaryotype with partial gonadal dysgenesis and gonadoblastoma. Hormone Research. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Costa EMF, Nishi MY, Pinto EM, Domenice S, Mendonça BB. A complex submicroscopic chromosomal imbalance in Xp 21,2 with microduplication and one microtriplication containing the DAX1 gene in a patient with 46,XY/47,XY,+markaryotype with partial gonadal dysgenesis and gonadoblastoma. Hormone Research. 2008 ; 70 69.[citado 2024 ago. 20 ]
Vancouver
Costa EMF, Nishi MY, Pinto EM, Domenice S, Mendonça BB. A complex submicroscopic chromosomal imbalance in Xp 21,2 with microduplication and one microtriplication containing the DAX1 gene in a patient with 46,XY/47,XY,+markaryotype with partial gonadal dysgenesis and gonadoblastoma. Hormone Research. 2008 ; 70 69.[citado 2024 ago. 20 ]
Artigo de periodico
Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment (2007)
Coutinho, Debora C.; Mendonça, Berenice B.; Coletta, Rocio R. D.; Costa, Elaine M. F.; Pachi, Paulo R.; Boguszewski, Margaret C. S.; Damiani, Durval; Arnhold, Ivo J. P.; Jorge, Alexander A. L.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: POLIMORFISMO, BIOLOGIA MOLECULAR, MUTAÇÃO GENÉTICA, NUCLEOTÍDEOS (ANÁLISE), CRESCIMENTO E DESENVOLVIMENTO (ESTUDO CLÍNICO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COUTINHO, Debora C. et al. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment. Journal of Clinical Endocrinology and Metabolism, v. 92, n. 12, p. 4889-4892, 2007Tradução . . Disponível em: https://doi.org/10.1210/jc.2007-1661. Acesso em: 20 ago. 2024.
APA
Coutinho, D. C., Mendonça, B. B., Coletta, R. R. D., Costa, E. M. F., Pachi, P. R., Boguszewski, M. C. S., et al. (2007). Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment. Journal of Clinical Endocrinology and Metabolism, 92( 12), 4889-4892. doi:10.1210/jc.2007-1661
NLM
Coutinho DC, Mendonça BB, Coletta RRD, Costa EMF, Pachi PR, Boguszewski MCS, Damiani D, Arnhold IJP, Jorge AAL. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment [Internet]. Journal of Clinical Endocrinology and Metabolism. 2007 ; 92( 12): 4889-4892.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1210/jc.2007-1661
Vancouver
Coutinho DC, Mendonça BB, Coletta RRD, Costa EMF, Pachi PR, Boguszewski MCS, Damiani D, Arnhold IJP, Jorge AAL. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment [Internet]. Journal of Clinical Endocrinology and Metabolism. 2007 ; 92( 12): 4889-4892.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1210/jc.2007-1661
Trabalho de evento-resumo
Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome (2007)
Abreu, Ana Paula; Trarbach, Ericka; Castro, Margaret de; Costa, Elaine M. F.; Versiani, Beatriz; Baptista, Maria Tereza M.; Garmes, Heraldo M.; Mendonça, Berenice B.; Latronico, Ana Claudia
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting (ENDO). Unidade: FMRP
Assunto: HIPOGONADISMO
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ABNT
ABREU, Ana Paula et al. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. 2007, Anais.. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2007. . Acesso em: 20 ago. 2024.
APA
Abreu, A. P., Trarbach, E., Castro, M. de, Costa, E. M. F., Versiani, B., Baptista, M. T. M., et al. (2007). Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. In Program and Abstracts. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Abreu AP, Trarbach E, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. Program and Abstracts. 2007 ;[citado 2024 ago. 20 ]
Vancouver
Abreu AP, Trarbach E, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. Program and Abstracts. 2007 ;[citado 2024 ago. 20 ]

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