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Trabalho de evento-resumo
Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence (2005)
Carvalho, Luciani R.; Antonini, Sonir Roberto Rauber; Castro, Margaret de; Arnhold, Ivo Jorge Prado; Mendonça, Berenice Bilharinho de
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidades: FMRP, FM
Assunto: ENDOCRINOLOGIA
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ABNT
CARVALHO, Luciani R. et al. Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence. 2005, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2005. . Acesso em: 05 nov. 2024.
APA
Carvalho, L. R., Antonini, S. R. R., Castro, M. de, Arnhold, I. J. P., & Mendonça, B. B. de. (2005). Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence. In Program and Abstracts. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Carvalho LR, Antonini SRR, Castro M de, Arnhold IJP, Mendonça BB de. Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence. Program and Abstracts. 2005 ;[citado 2024 nov. 05 ]
Vancouver
Carvalho LR, Antonini SRR, Castro M de, Arnhold IJP, Mendonça BB de. Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence. Program and Abstracts. 2005 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis (2004)
Melo, Maria E; Marui, Suemi; Gomes, Miriam C; Arnhold, Ivo J; Mendonça, Berenice Bilharinho de; Knopfelmacher, Mirta
Source: Program and Abstracts. Conference titles: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: DIFERENCIAÇÃO CELULCAR, MUTAÇÃO GENÉTICA, POLIMORFISMO, HIPÓFISE (ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Maria E et al. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 05 nov. 2024.
APA
Melo, M. E., Marui, S., Gomes, M. C., Arnhold, I. J., Mendonça, B. B. de, & Knopfelmacher, M. (2004). Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Melo ME, Marui S, Gomes MC, Arnhold IJ, Mendonça BB de, Knopfelmacher M. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Vancouver
Melo ME, Marui S, Gomes MC, Arnhold IJ, Mendonça BB de, Knopfelmacher M. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors (2004)
Pinto, Emilia M; Billerbeck, Ana Elisa C; Fragoso, Maria Candida B. V; Domenice, Sorahia; Mendonça, Berenice Bilharinho de; Latronico, Ana Claudia
Source: Program and Abstracts. Conference titles: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: BIOMARCADORES, MUTAÇÃO GENÉTICA, POLIMORFISMO, BRASILEIROS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINTO, Emilia M et al. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 05 nov. 2024.
APA
Pinto, E. M., Billerbeck, A. E. C., Fragoso, M. C. B. V., Domenice, S., Mendonça, B. B. de, & Latronico, A. C. (2004). Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Pinto EM, Billerbeck AEC, Fragoso MCBV, Domenice S, Mendonça BB de, Latronico AC. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Vancouver
Pinto EM, Billerbeck AEC, Fragoso MCBV, Domenice S, Mendonça BB de, Latronico AC. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome (2004)
d'Alva, Catarina B; Serafini, Paulo; Motta, Eduardo; Koherk, Maria Beatriz F; Latronico, Ana Claudia; Mendonça, Berenice Bilharinho de
Source: Program and Abstracts. Conference titles: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: FERTILIZAÇÃO (TERAPIA), MUTAÇÃO GENÉTICA, POLIMORFISMO, OVÁRIO (FISIOPATOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
D'ALVA, Catarina B et al. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 05 nov. 2024.
APA
d'Alva, C. B., Serafini, P., Motta, E., Koherk, M. B. F., Latronico, A. C., & Mendonça, B. B. de. (2004). No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
d'Alva CB, Serafini P, Motta E, Koherk MBF, Latronico AC, Mendonça BB de. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Vancouver
d'Alva CB, Serafini P, Motta E, Koherk MBF, Latronico AC, Mendonça BB de. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency (2002)
Castro, Margaret de; Penachioni, Junia Y.; Bachega, Tania A. S. S.; Mendonça, Berenice Bilharinho de; Fernandes, Vania F. T.; Kater, Claudio E.; Longui, Carlos A.; Moreira, Ayrton Custódio; Mello, Maricilda P.
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidades: FMRP, FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Margaret de et al. Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency. 2002, Anais.. San Francisco: Endocrine Society, 2002. . Acesso em: 05 nov. 2024.
APA
Castro, M. de, Penachioni, J. Y., Bachega, T. A. S. S., Mendonça, B. B. de, Fernandes, V. F. T., Kater, C. E., et al. (2002). Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency. In Program and Abstracts. San Francisco: Endocrine Society.
NLM
Castro M de, Penachioni JY, Bachega TASS, Mendonça BB de, Fernandes VFT, Kater CE, Longui CA, Moreira AC, Mello MP. Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency. Program and Abstracts. 2002 ;[citado 2024 nov. 05 ]
Vancouver
Castro M de, Penachioni JY, Bachega TASS, Mendonça BB de, Fernandes VFT, Kater CE, Longui CA, Moreira AC, Mello MP. Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency. Program and Abstracts. 2002 ;[citado 2024 nov. 05 ]

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