ReP USP - Resultado da busca

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)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 nov. 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 nov. 01 ] 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 nov. 01 ] 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)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 nov. 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 nov. 01 ] 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 nov. 01 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618
Artigo de periodico
TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood (2010)
Gianetti, Elena; Tusset, Cintia; Noel, Sekoni D.; Au, Margaret G.; Dwyer, Andrew A.; Hughes, Virginia A.; Abreu, Ana Paula; Carroll, Jessica; Trarbach, Ericka; Silveira, Leticia F. G.; Costa, Elaine M. F.; Mendonça, Berenice Bilharinho de; Castro, Margaret de; Lofrano, Adriana; Hall, Janet E.; Bolu, Erol; Ozata, Metin; Quinton, Richard; Amory, John K.; Stewart, Susan E.; Arlt, Wiebke; Cole, Trevor R.; Crowley, William F.; Kaiser, Ursula B.; Latronico, Ana Claudia; Seminara, Stephanie B.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES (ANÁLISE), GONADOTROFINAS (METABOLISMO), FENÓTIPOS, HIPOGONADISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIANETTI, Elena et al. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 5, p. 2857-2867, 2010Tradução . . Disponível em: https://doi.org/10.1210/jc.2009-2320. Acesso em: 01 nov. 2024.
APA
Gianetti, E., Tusset, C., Noel, S. D., Au, M. G., Dwyer, A. A., Hughes, V. A., et al. (2010). TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood. Journal of Clinical Endocrinology and Metabolism, 95( 5), 2857-2867. doi:10.1210/jc.2009-2320
NLM
Gianetti E, Tusset C, Noel SD, Au MG, Dwyer AA, Hughes VA, Abreu AP, Carroll J, Trarbach E, Silveira LFG, Costa EMF, Mendonça BB de, Castro M de, Lofrano A, Hall JE, Bolu E, Ozata M, Quinton R, Amory JK, Stewart SE, Arlt W, Cole TR, Crowley WF, Kaiser UB, Latronico AC, Seminara SB. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2857-2867.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2009-2320
Vancouver
Gianetti E, Tusset C, Noel SD, Au MG, Dwyer AA, Hughes VA, Abreu AP, Carroll J, Trarbach E, Silveira LFG, Costa EMF, Mendonça BB de, Castro M de, Lofrano A, Hall JE, Bolu E, Ozata M, Quinton R, Amory JK, Stewart SE, Arlt W, Cole TR, Crowley WF, Kaiser UB, Latronico AC, Seminara SB. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2857-2867.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2009-2320
Artigo de periodico
Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency (2010)
Trarbach, Ericka B.; Abreu, Ana Paula; Silveira, Leticia Ferreira Gontijo; Garmes, Heraldo Mendes; Baptista, Maria Tereza M.; Teles, Milena Gurgel; Costa, Elaine M. F.; Mohammadi, Moosa; Pitteloud, Nelly; Mendonça, Berenice Bilharinho; Latronico, Ana Claudia
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GÊNICA, GONADOTROFINAS (DEFICIÊNCIA), REAÇÃO EM CADEIA POR POLIMERASE, ENDOCRINOPATIAS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TRARBACH, Ericka B. et al. Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 7, p. 3491-3496, 2010Tradução . . Disponível em: https://doi.org/10.1210/jc.2010-0176. Acesso em: 01 nov. 2024.
APA
Trarbach, E. B., Abreu, A. P., Silveira, L. F. G., Garmes, H. M., Baptista, M. T. M., Teles, M. G., et al. (2010). Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency. Journal of Clinical Endocrinology and Metabolism, 95( 7), 3491-3496. doi:10.1210/jc.2010-0176
NLM
Trarbach EB, Abreu AP, Silveira LFG, Garmes HM, Baptista MTM, Teles MG, Costa EMF, Mohammadi M, Pitteloud N, Mendonça BB, Latronico AC. Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 7): 3491-3496.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2010-0176
Vancouver
Trarbach EB, Abreu AP, Silveira LFG, Garmes HM, Baptista MTM, Teles MG, Costa EMF, Mohammadi M, Pitteloud N, Mendonça BB, Latronico AC. Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 7): 3491-3496.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2010-0176
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 nov. 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 nov. 01 ]
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 nov. 01 ]

USP Schools

ReP

Filtros

Authors

Subjects

Indexado em