ReP USP - Resultado da busca

Trabalho de evento-resumo
Missense mutation in the lh receptor gene causas leydig cell hypoplasia (1995)
Themmen, A P N; Kraais, R; Kremer, H; Post, M; Toledo, S. P. A.; Brunner, H G; Grootegoed, J A
Fonte: Program and Abstracts. Nome do evento: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
THEMMEN, A P N et al. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 23 ago. 2024.
APA
Themmen, A. P. N., Kraais, R., Kremer, H., Post, M., Toledo, S. P. A., Brunner, H. G., & Grootegoed, J. A. (1995). Missense mutation in the lh receptor gene causas leydig cell hypoplasia. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2024 ago. 23 ]
Vancouver
Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2024 ago. 23 ]
Trabalho de evento-resumo
Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients (1995)
Borges, M F; Abelin, N M A; Barros, M A E; Resende, E A M; Toledo, S. P. A.
Fonte: Program and Abstracts. Nome do evento: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BORGES, M F et al. Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients. 1995, Anais.. Washington: Endocrine Society, 1995. . Acesso em: 23 ago. 2024.
APA
Borges, M. F., Abelin, N. M. A., Barros, M. A. E., Resende, E. A. M., & Toledo, S. P. A. (1995). Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients. In Program and Abstracts. Washington: Endocrine Society.
NLM
Borges MF, Abelin NMA, Barros MAE, Resende EAM, Toledo SPA. Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients. Program and Abstracts. 1995 ;[citado 2024 ago. 23 ]
Vancouver
Borges MF, Abelin NMA, Barros MAE, Resende EAM, Toledo SPA. Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients. Program and Abstracts. 1995 ;[citado 2024 ago. 23 ]
Artigo de periodico
Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas (1995)
Eng, C; Crossey, P A; Mulligan, L M; Healey, C S; Houghton, C; Prowse, A; Chew, S L; Dahia, P L M; Oriordan, J L H; Toledo, S. P. A.; Smith, D P; Maher, E R
Fonte: Journal of Medical Genetics. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ENG, C et al. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, v. 32, n. 12, p. 934-7, 1995Tradução . . Disponível em: https://doi.org/10.1136/jmg.32.12.934. Acesso em: 23 ago. 2024.
APA
Eng, C., Crossey, P. A., Mulligan, L. M., Healey, C. S., Houghton, C., Prowse, A., et al. (1995). Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, 32( 12), 934-7. doi:10.1136/jmg.32.12.934
NLM
Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1136/jmg.32.12.934
Vancouver
Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1136/jmg.32.12.934
Dissertação (Mestrado)
Estudo cito-histopatológico do carcinoma medular da tireóide: aspectos clínicos, morfológicos e imunorreativos (1995)
Cravero, Nanci Paula; Bisi, Hélio (Orientador); Toledo, S. P. A. (Orientador)
Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CRAVERO, Nanci Paula. Estudo cito-histopatológico do carcinoma medular da tireóide: aspectos clínicos, morfológicos e imunorreativos. 1995. Dissertação (Mestrado) – Universidade de São Paulo, São Paulo, 1995. . Acesso em: 23 ago. 2024.
APA
Cravero, N. P. (1995). Estudo cito-histopatológico do carcinoma medular da tireóide: aspectos clínicos, morfológicos e imunorreativos (Dissertação (Mestrado). Universidade de São Paulo, São Paulo.
NLM
Cravero NP. Estudo cito-histopatológico do carcinoma medular da tireóide: aspectos clínicos, morfológicos e imunorreativos. 1995 ;[citado 2024 ago. 23 ]
Vancouver
Cravero NP. Estudo cito-histopatológico do carcinoma medular da tireóide: aspectos clínicos, morfológicos e imunorreativos. 1995 ;[citado 2024 ago. 23 ]
Artigo de periodico
Adrenocortical function in old age: cortisol response to submaximal stimulation with adrenocorticotropin (1995)
Malerbi, D A C; Jacob Filho, Wilson; Toledo, S. P. A.; Mendonça, B. B.; Virches, C S; Corradinim, M C; Geiss, E R; Carvalho Filho, E. T.; Wajchenberg, B L
Fonte: Endocrinology and Metabolism. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MALERBI, D A C et al. Adrenocortical function in old age: cortisol response to submaximal stimulation with adrenocorticotropin. Endocrinology and Metabolism, v. 2 , p. 245-9, 1995Tradução . . Acesso em: 23 ago. 2024.
APA
Malerbi, D. A. C., Jacob Filho, W., Toledo, S. P. A., Mendonça, B. B., Virches, C. S., Corradinim, M. C., et al. (1995). Adrenocortical function in old age: cortisol response to submaximal stimulation with adrenocorticotropin. Endocrinology and Metabolism, 2 , 245-9.
NLM
Malerbi DAC, Jacob Filho W, Toledo SPA, Mendonça BB, Virches CS, Corradinim MC, Geiss ER, Carvalho Filho ET, Wajchenberg BL. Adrenocortical function in old age: cortisol response to submaximal stimulation with adrenocorticotropin. Endocrinology and Metabolism. 1995 ;2 245-9.[citado 2024 ago. 23 ]
Vancouver
Malerbi DAC, Jacob Filho W, Toledo SPA, Mendonça BB, Virches CS, Corradinim MC, Geiss ER, Carvalho Filho ET, Wajchenberg BL. Adrenocortical function in old age: cortisol response to submaximal stimulation with adrenocorticotropin. Endocrinology and Metabolism. 1995 ;2 245-9.[citado 2024 ago. 23 ]
Trabalho de evento-resumo
Molecular analysis of p53 vhl and ret genes in pheochromocytoma (1995)
Dahia, P L M; Aguiar, R C T; Eng, C; Crossey, P A; Maher, E R; Grossman, A; Ponder, B A J; Toledo, S. P. A.
Fonte: Program and Abstracts. Nome do evento: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DAHIA, P L M et al. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 23 ago. 2024.
APA
Dahia, P. L. M., Aguiar, R. C. T., Eng, C., Crossey, P. A., Maher, E. R., Grossman, A., et al. (1995). Molecular analysis of p53 vhl and ret genes in pheochromocytoma. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Dahia PLM, Aguiar RCT, Eng C, Crossey PA, Maher ER, Grossman A, Ponder BAJ, Toledo SPA. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. Program and Abstracts. 1995 ;[citado 2024 ago. 23 ]
Vancouver
Dahia PLM, Aguiar RCT, Eng C, Crossey PA, Maher ER, Grossman A, Ponder BAJ, Toledo SPA. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. Program and Abstracts. 1995 ;[citado 2024 ago. 23 ]
Trabalho de evento-resumo periodico
Lack of evidence of p53 involvement in phaeochromocytoma oncogenesis (1995)
Dahia, P L M; Tsanaclis, Ana Maria Crous; Ezabella, M C L; Hayashida, C Y; Abelin, N M A; Toledo, S. P. A.
Fonte: Journal of Endocrinology. Nome do evento: Joint Meeting of the British Endocrine Societies and European Federation of Endocrine Societies. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DAHIA, P L M et al. Lack of evidence of p53 involvement in phaeochromocytoma oncogenesis. Journal of Endocrinology. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 23 ago. 2024. , 1995
APA
Dahia, P. L. M., Tsanaclis, A. M. C., Ezabella, M. C. L., Hayashida, C. Y., Abelin, N. M. A., & Toledo, S. P. A. (1995). Lack of evidence of p53 involvement in phaeochromocytoma oncogenesis. Journal of Endocrinology. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Dahia PLM, Tsanaclis AMC, Ezabella MCL, Hayashida CY, Abelin NMA, Toledo SPA. Lack of evidence of p53 involvement in phaeochromocytoma oncogenesis. Journal of Endocrinology. 1995 ;144( suppl.):[citado 2024 ago. 23 ]
Vancouver
Dahia PLM, Tsanaclis AMC, Ezabella MCL, Hayashida CY, Abelin NMA, Toledo SPA. Lack of evidence of p53 involvement in phaeochromocytoma oncogenesis. Journal of Endocrinology. 1995 ;144( suppl.):[citado 2024 ago. 23 ]
Artigo de periodico
Molecular and immunohistochemical analysis of p53 in phaeochromocytoma (1995)
Dahia, P L M; Aguiar, R C T; Tsanaclis, Ana Maria Crous; Bendit, I; Bydlowski, Sérgio Paulo; Abelin, N M A; Toledo, S. P. A.
Fonte: British Journal of Cancer. Unidade: FM
Assunto: PATOLOGIA CLÍNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DAHIA, P L M et al. Molecular and immunohistochemical analysis of p53 in phaeochromocytoma. British Journal of Cancer, v. no 1995, n. 5 , p. 1211-3, 1995Tradução . . Disponível em: https://doi.org/10.1038/bjc.1995.487. Acesso em: 23 ago. 2024.
APA
Dahia, P. L. M., Aguiar, R. C. T., Tsanaclis, A. M. C., Bendit, I., Bydlowski, S. P., Abelin, N. M. A., & Toledo, S. P. A. (1995). Molecular and immunohistochemical analysis of p53 in phaeochromocytoma. British Journal of Cancer, no 1995( 5 ), 1211-3. doi:10.1038/bjc.1995.487
NLM
Dahia PLM, Aguiar RCT, Tsanaclis AMC, Bendit I, Bydlowski SP, Abelin NMA, Toledo SPA. Molecular and immunohistochemical analysis of p53 in phaeochromocytoma [Internet]. British Journal of Cancer. 1995 ; no 1995( 5 ): 1211-3.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1038/bjc.1995.487
Vancouver
Dahia PLM, Aguiar RCT, Tsanaclis AMC, Bendit I, Bydlowski SP, Abelin NMA, Toledo SPA. Molecular and immunohistochemical analysis of p53 in phaeochromocytoma [Internet]. British Journal of Cancer. 1995 ; no 1995( 5 ): 1211-3.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1038/bjc.1995.487
Artigo de periodico
Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene (1995)
Kremer, H; Kraaij, R; Toledo, S. P. A.; Post, M; Fridman, J B; Hayashida, C Y; Reen, M; Milgrom, E.; Ropers, H H; Mariman, E; Themmen, A P N; Brunner, H G
Fonte: Nature Genetics. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KREMER, H et al. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nature Genetics, v. 9 , p. 160-4, 1995Tradução . . Disponível em: https://doi.org/10.1038/ng0295-160. Acesso em: 23 ago. 2024.
APA
Kremer, H., Kraaij, R., Toledo, S. P. A., Post, M., Fridman, J. B., Hayashida, C. Y., et al. (1995). Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene. Nature Genetics, 9 , 160-4. doi:10.1038/ng0295-160
NLM
Kremer H, Kraaij R, Toledo SPA, Post M, Fridman JB, Hayashida CY, Reen M, Milgrom E, Ropers HH, Mariman E, Themmen APN, Brunner HG. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene [Internet]. Nature Genetics. 1995 ;9 160-4.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1038/ng0295-160
Vancouver
Kremer H, Kraaij R, Toledo SPA, Post M, Fridman JB, Hayashida CY, Reen M, Milgrom E, Ropers HH, Mariman E, Themmen APN, Brunner HG. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene [Internet]. Nature Genetics. 1995 ;9 160-4.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1038/ng0295-160

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