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Artigo de periodico
Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation (2012)
Domenice, Sorahia; Brito, Vinicius N.; Cukier, Priscila; Arnold, Ivo J. P.; Nishi, Mirian Y.; Latronico, Ana C.; Mendonca, Berenice B.
Source: Endocrine Reviews. Conference titles: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo. Unidade: FM
Subjects: PUBERDADE PRECOCE, CARCINOMA, MUTAÇÃO GENÉTICA, HIPOGONADISMO, SEXUALIDADE, FENÓTIPOS, GONADOTROFINAS HIPOFISÁRIAS (ANÁLISE), RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DOMENICE, Sorahia et al. Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-622. Acesso em: 01 nov. 2024.
APA
Domenice, S., Brito, V. N., Cukier, P., Arnold, I. J. P., Nishi, M. Y., Latronico, A. C., & Mendonca, B. B. (2012). Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-622
NLM
Domenice S, Brito VN, Cukier P, Arnold IJP, Nishi MY, Latronico AC, Mendonca BB. Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 nov. 01 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-622
Vancouver
Domenice S, Brito VN, Cukier P, Arnold IJP, Nishi MY, Latronico AC, Mendonca BB. Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 nov. 01 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-622
Artigo de periodico
Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 (2012)
Montenegro, Luciana R.; Leal, Andrea C.; Coutinho, Debora C.; Valassi, Helena P. L.; Nishi, Mirian Y.; Arnhold, Ivo J. P.; Mendonca, Berenice B.; Jorge, Alexander A. L.
Source: European Journal of Endocrinology. Unidade: FM
Subjects: METABOLISMO (QUÍMICA), PROLIFERAÇÃO CELULAR, CULTURA DE CÉLULAS, FENÓTIPOS, REAÇÃO EM CADEIA POR POLIMERASE, ANORMALIDADES MUSCULOSQUELÉTICAS (GENÉTICA), BIOQUÍMICA CLÍNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONTENEGRO, Luciana R. et al. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11. European Journal of Endocrinology, v. 166, n. 3, p. 543-550, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0964. Acesso em: 01 nov. 2024.
APA
Montenegro, L. R., Leal, A. C., Coutinho, D. C., Valassi, H. P. L., Nishi, M. Y., Arnhold, I. J. P., et al. (2012). Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11. European Journal of Endocrinology, 166( 3), 543-550. doi:10.1530/EJE-11-0964
NLM
Montenegro LR, Leal AC, Coutinho DC, Valassi HPL, Nishi MY, Arnhold IJP, Mendonca BB, Jorge AAL. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 [Internet]. European Journal of Endocrinology. 2012 ; 166( 3): 543-550.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1530/EJE-11-0964
Vancouver
Montenegro LR, Leal AC, Coutinho DC, Valassi HPL, Nishi MY, Arnhold IJP, Mendonca BB, Jorge AAL. Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11 [Internet]. European Journal of Endocrinology. 2012 ; 166( 3): 543-550.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1530/EJE-11-0964
Artigo de periodico
GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects (2012)
Marui, Suemi; Trabach, Ericka b.; Boguszewski, Margaret C. S.; França, Marcela M.; Jorge, Alexander A. L.; Inoue, Hiroshi; Nishi, Mirian Y.; Lacerda Filho, Luiz de; Aguiar-Oliveira, Manuel H.; Mendonça, Berenice B.; Arnhold, Ivo J. P.
Source: Hormone research in paediatrics. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES (ANÁLISE), HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), DNA (ANÁLISE), AMPLIFICAÇÃO DE GENES, RECEPTORES HORMONAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARUI, Suemi et al. GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects. Hormone research in paediatrics, v. 78, n. 3, p. 165-172, 2012Tradução . . Disponível em: https://doi.org/10.1159/000342760. Acesso em: 01 nov. 2024.
APA
Marui, S., Trabach, E. b., Boguszewski, M. C. S., França, M. M., Jorge, A. A. L., Inoue, H., et al. (2012). GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects. Hormone research in paediatrics, 78( 3), 165-172. doi:10.1159/000342760
NLM
Marui S, Trabach E b., Boguszewski MCS, França MM, Jorge AAL, Inoue H, Nishi MY, Lacerda Filho L de, Aguiar-Oliveira MH, Mendonça BB, Arnhold IJP. GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects [Internet]. Hormone research in paediatrics. 2012 ;78( 3): 165-172.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1159/000342760
Vancouver
Marui S, Trabach E b., Boguszewski MCS, França MM, Jorge AAL, Inoue H, Nishi MY, Lacerda Filho L de, Aguiar-Oliveira MH, Mendonça BB, Arnhold IJP. GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects [Internet]. Hormone research in paediatrics. 2012 ;78( 3): 165-172.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1159/000342760

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