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Artigo de periodico
Could the less-than subtotal parathyroidectomy be an Option for treating young patients with multiple endocrine neoplasia Type 1-related hyperparathyroidism? (2019)
Montenegro, Fabio Luiz de Menezes; Brescia, Manilla D'Elboux Guimaraes; Jr, Delmar Muniz Lourenco; Arap, Sergio Samir; D'alessandro, Andre Fernandes; Silva Filho, Gilberto de Britto e; Toledo, Sergio Pereira de Almeida
Fonte: Frontiers in endocrinology. Unidade: FM
Assuntos: PARATIREOIDECTOMIA, NEOPLASIAS DAS PARATIREOIDES, ADOLESCENTES
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ABNT
MONTENEGRO, Fabio Luiz de Menezes et al. Could the less-than subtotal parathyroidectomy be an Option for treating young patients with multiple endocrine neoplasia Type 1-related hyperparathyroidism?. Frontiers in endocrinology, v. 10, 2019Tradução . . Disponível em: https://doi.org/10.3389/fendo.2019.00123. Acesso em: 15 maio 2024.
APA
Montenegro, F. L. de M., Brescia, M. D. 'E. G., Jr, D. M. L., Arap, S. S., D'alessandro, A. F., Silva Filho, G. de B. e, & Toledo, S. P. de A. (2019). Could the less-than subtotal parathyroidectomy be an Option for treating young patients with multiple endocrine neoplasia Type 1-related hyperparathyroidism? Frontiers in endocrinology, 10. doi:10.3389/fendo.2019.00123
NLM
Montenegro FL de M, Brescia MD'EG, Jr DML, Arap SS, D'alessandro AF, Silva Filho G de B e, Toledo SP de A. Could the less-than subtotal parathyroidectomy be an Option for treating young patients with multiple endocrine neoplasia Type 1-related hyperparathyroidism? [Internet]. Frontiers in endocrinology. 2019 ; 10[citado 2024 maio 15 ] Available from: https://doi.org/10.3389/fendo.2019.00123
Vancouver
Montenegro FL de M, Brescia MD'EG, Jr DML, Arap SS, D'alessandro AF, Silva Filho G de B e, Toledo SP de A. Could the less-than subtotal parathyroidectomy be an Option for treating young patients with multiple endocrine neoplasia Type 1-related hyperparathyroidism? [Internet]. Frontiers in endocrinology. 2019 ; 10[citado 2024 maio 15 ] Available from: https://doi.org/10.3389/fendo.2019.00123
Artigo de periodico
Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study (2019)
Maciel, Rui M. B; Camacho, Cleber P; Assumpção, Ligia V. M; Bufalo, Natassia E; Carvalho, Andre L; Carvalho, Gisah A. de; Castroneves, Luciana A; Junior, Francisco M. de Castro; Jorge, Alexander Augusto de Lima; Toledo, Sergio Pereira de Almeida; Maciel, Léa Maria Zanini
Fonte: Endocrine Connections. Unidades: FM, FMRP
Assuntos: GENÓTIPOS, FENÓTIPOS, NEOPLASIAS DA TIREOIDE, CARCINOMA MEDULAR
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ABNT
MACIEL, Rui M. B et al. Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study. Endocrine Connections, v. 8, n. 3, p. 289-298, 2019Tradução . . Disponível em: https://doi.org/10.1530/EC-18-0506. Acesso em: 15 maio 2024.
APA
Maciel, R. M. B., Camacho, C. P., Assumpção, L. V. M., Bufalo, N. E., Carvalho, A. L., Carvalho, G. A. de, et al. (2019). Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study. Endocrine Connections, 8( 3), 289-298. doi:10.1530/EC-18-0506
NLM
Maciel RMB, Camacho CP, Assumpção LVM, Bufalo NE, Carvalho AL, Carvalho GA de, Castroneves LA, Junior FM de C, Jorge AA de L, Toledo SP de A, Maciel LMZ. Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study [Internet]. Endocrine Connections. 2019 ; 8( 3): 289-298.[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/EC-18-0506
Vancouver
Maciel RMB, Camacho CP, Assumpção LVM, Bufalo NE, Carvalho AL, Carvalho GA de, Castroneves LA, Junior FM de C, Jorge AA de L, Toledo SP de A, Maciel LMZ. Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study [Internet]. Endocrine Connections. 2019 ; 8( 3): 289-298.[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/EC-18-0506
Artigo de periodico
Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing (2018)
Carvalho, Rafael A.; Jorge, Alexander Augusto de Lima; Toledo, Sergio Pereira de Almeida
Fonte: European journal of endocrinology. Unidade: FM
Assuntos: NEOPLASIAS DAS PARATIREOIDES, MUTAÇÃO GENÉTICA, SEQUENCIAMENTO GENÉTICO
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ABNT
CARVALHO, Rafael A. e JORGE, Alexander Augusto de Lima e TOLEDO, Sergio Pereira de Almeida. Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing. European journal of endocrinology, v. 179, n. 6, p. 391-407, 2018Tradução . . Disponível em: https://doi.org/10.1530/EJE-18-0430. Acesso em: 15 maio 2024.
APA
Carvalho, R. A., Jorge, A. A. de L., & Toledo, S. P. de A. (2018). Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing. European journal of endocrinology, 179( 6), 391-407. doi:10.1530/EJE-18-0430
NLM
Carvalho RA, Jorge AA de L, Toledo SP de A. Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing [Internet]. European journal of endocrinology. 2018 ; 179( 6): 391-407.[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/EJE-18-0430
Vancouver
Carvalho RA, Jorge AA de L, Toledo SP de A. Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing [Internet]. European journal of endocrinology. 2018 ; 179( 6): 391-407.[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/EJE-18-0430
Parte de monografia/livro
Neoplasia endócrina múltipla tipo 1 (2017)
Lourenço Júnior, Delmar Muniz; Toledo, Rodrigo de Almeida; Toledo, Sérgio Pereira de Almeida
Fonte: Endocrinologia : princípios e práticas. Unidade: FM
Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA, NEOPLASIAS PANCREÁTICAS, PREVALÊNCIA
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ABNT
LOURENÇO JÚNIOR, Delmar Muniz e TOLEDO, Rodrigo de Almeida e TOLEDO, Sérgio Pereira de Almeida. Neoplasia endócrina múltipla tipo 1. Endocrinologia : princípios e práticas. Tradução . Rio de Janeiro: Atheneu, 2017. . . Acesso em: 15 maio 2024.
APA
Lourenço Júnior, D. M., Toledo, R. de A., & Toledo, S. P. de A. (2017). Neoplasia endócrina múltipla tipo 1. In Endocrinologia : princípios e práticas. Rio de Janeiro: Atheneu.
NLM
Lourenço Júnior DM, Toledo R de A, Toledo SP de A. Neoplasia endócrina múltipla tipo 1. In: Endocrinologia : princípios e práticas. Rio de Janeiro: Atheneu; 2017. [citado 2024 maio 15 ]
Vancouver
Lourenço Júnior DM, Toledo R de A, Toledo SP de A. Neoplasia endócrina múltipla tipo 1. In: Endocrinologia : princípios e práticas. Rio de Janeiro: Atheneu; 2017. [citado 2024 maio 15 ]
Parte de monografia/livro
Neoplasias endócrinas múltiplas (2016)
Lourenço Junior, Delmar Muniz; Hoff, Ana Amélia Fialho de Oliveira; Perez, Ricardo Vessoni; Toledo, Rodrigo de Almeida; Toledo, Sergio Pereira de Almeida
Fonte: Clínica Médica/vol. 5. Unidade: FM
Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA (DIAGNÓSTICO), SEGUIMENTOS, MUTAÇÃO GENÉTICA (PREVALÊNCIA;DIAGNÓSTICO)
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ABNT
LOURENÇO JUNIOR, Delmar Muniz et al. Neoplasias endócrinas múltiplas. Clínica Médica/vol. 5. Tradução . Barueri, SP: Manole, 2016. . . Acesso em: 15 maio 2024.
APA
Lourenço Junior, D. M., Hoff, A. A. F. de O., Perez, R. V., Toledo, R. de A., & Toledo, S. P. de A. (2016). Neoplasias endócrinas múltiplas. In Clínica Médica/vol. 5. Barueri, SP: Manole.
NLM
Lourenço Junior DM, Hoff AAF de O, Perez RV, Toledo R de A, Toledo SP de A. Neoplasias endócrinas múltiplas. In: Clínica Médica/vol. 5. Barueri, SP: Manole; 2016. [citado 2024 maio 15 ]
Vancouver
Lourenço Junior DM, Hoff AAF de O, Perez RV, Toledo R de A, Toledo SP de A. Neoplasias endócrinas múltiplas. In: Clínica Médica/vol. 5. Barueri, SP: Manole; 2016. [citado 2024 maio 15 ]
Artigo de periodico-carta/editorial
RET Y791F: alone or accompanied? [Carta] (2015)
Toledo, Rodrigo A.; Loureço Jr., Delmar M.; Camacho, Cleber; Lindsey, Susan; Cerutti, Janete; Maciel, Rui M. B.; Toledo, Sergio P. A.
Fonte: Archives of Endocrinology and Metabolism. Unidade: FM
Assuntos: BRASILEIROS, MUTAÇÃO GENÉTICA, TIREOIDECTOMIA
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ABNT
TOLEDO, Rodrigo A. et al. RET Y791F: alone or accompanied? [Carta]. Archives of Endocrinology and Metabolism. São Paulo: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1590/2359-3997000000060. Acesso em: 15 maio 2024. , 2015
APA
Toledo, R. A., Loureço Jr., D. M., Camacho, C., Lindsey, S., Cerutti, J., Maciel, R. M. B., & Toledo, S. P. A. (2015). RET Y791F: alone or accompanied? [Carta]. Archives of Endocrinology and Metabolism. São Paulo: Faculdade de Medicina, Universidade de São Paulo. doi:10.1590/2359-3997000000060
NLM
Toledo RA, Loureço Jr. DM, Camacho C, Lindsey S, Cerutti J, Maciel RMB, Toledo SPA. RET Y791F: alone or accompanied? [Carta] [Internet]. Archives of Endocrinology and Metabolism. 2015 ; 59( 5): 476-477.[citado 2024 maio 15 ] Available from: https://doi.org/10.1590/2359-3997000000060
Vancouver
Toledo RA, Loureço Jr. DM, Camacho C, Lindsey S, Cerutti J, Maciel RMB, Toledo SPA. RET Y791F: alone or accompanied? [Carta] [Internet]. Archives of Endocrinology and Metabolism. 2015 ; 59( 5): 476-477.[citado 2024 maio 15 ] Available from: https://doi.org/10.1590/2359-3997000000060
Artigo de periodico
Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility (2015)
Toledo, Rodrigo A.; Hatakana, Roxanne; Lourenço Jr, Delmar M.; Lindsey, Susan C.; Camacho, Cleber P.; Almeida, Marcio; Lima Jr, José V.; Sekiya, Tomoko; Garralda, Elena; Naslavsky, Michel ; Yamamoto, Guilherme L.; Lazar, Monize; Meirelles, Osorio; Sobreira, Tiago J. P.; Lebrao, Maria Lucia; Duarte, Yeda Aparecida de Oliveira ; Blangero, John; Zatz, Mayana ; Cerutti, Janete M.; Maciel, Rui M. B.; Toledo, Sergio P. A.
Fonte: Endocrine - Related Cancer. Unidades: FSP, EE, IB, FM
Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA, PROTO-ONCOGENES
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ABNT
TOLEDO, Rodrigo A. et al. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility. Endocrine - Related Cancer, v. 22, n. 2, 2015Tradução . . Disponível em: https://doi.org/10.1530/ERC-14-0491. Acesso em: 15 maio 2024.
APA
Toledo, R. A., Hatakana, R., Lourenço Jr, D. M., Lindsey, S. C., Camacho, C. P., Almeida, M., et al. (2015). Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility. Endocrine - Related Cancer, 22( 2). doi:10.1530/ERC-14-0491
NLM
Toledo RA, Hatakana R, Lourenço Jr DM, Lindsey SC, Camacho CP, Almeida M, Lima Jr JV, Sekiya T, Garralda E, Naslavsky M, Yamamoto GL, Lazar M, Meirelles O, Sobreira TJP, Lebrao ML, Duarte YA de O, Blangero J, Zatz M, Cerutti JM, Maciel RMB, Toledo SPA. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility [Internet]. Endocrine - Related Cancer. 2015 ; 22( 2):[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/ERC-14-0491
Vancouver
Toledo RA, Hatakana R, Lourenço Jr DM, Lindsey SC, Camacho CP, Almeida M, Lima Jr JV, Sekiya T, Garralda E, Naslavsky M, Yamamoto GL, Lazar M, Meirelles O, Sobreira TJP, Lebrao ML, Duarte YA de O, Blangero J, Zatz M, Cerutti JM, Maciel RMB, Toledo SPA. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility [Internet]. Endocrine - Related Cancer. 2015 ; 22( 2):[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/ERC-14-0491
Artigo de periodico
Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation (2015)
Toledo, Sergio P. A.; Lourenço Jr., Delmar M.; Sekiya, Tomoko; Lucon, Antonio M.; Baena, Marcos E. S.; Castro, Claudio C.; Bortolotto, Luiz A.; Zerbibi, Maria C. N.; Siqueira, Sheila A. C.; Toledo, Rodrigo A.; Dahia, Patricia L. M.
Fonte: The Journal of clinical endocrinology and metabolism. Unidade: FM
Assuntos: NEOPLASIAS EMBRIONÁRIAS DE CÉLULAS GERMINATIVAS, MUTAÇÃO GENÉTICA, GAMETAS, VARIAÇÃO GENÉTICA, FEOCROMOCITOMA
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ABNT
TOLEDO, Sergio P. A. et al. Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation. The Journal of clinical endocrinology and metabolism, v. 100, n. 2, p. E308-E318, 2015Tradução . . Disponível em: http://press.endocrine.org/doi/pdf/10.1210/jc.2014-2473. Acesso em: 15 maio 2024.
APA
Toledo, S. P. A., Lourenço Jr., D. M., Sekiya, T., Lucon, A. M., Baena, M. E. S., Castro, C. C., et al. (2015). Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation. The Journal of clinical endocrinology and metabolism, 100( 2), E308-E318. doi:10.1210/jc.2014-2473
NLM
Toledo SPA, Lourenço Jr. DM, Sekiya T, Lucon AM, Baena MES, Castro CC, Bortolotto LA, Zerbibi MCN, Siqueira SAC, Toledo RA, Dahia PLM. Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation [Internet]. The Journal of clinical endocrinology and metabolism. 2015 ; 100( 2): E308-E318.[citado 2024 maio 15 ] Available from: http://press.endocrine.org/doi/pdf/10.1210/jc.2014-2473
Vancouver
Toledo SPA, Lourenço Jr. DM, Sekiya T, Lucon AM, Baena MES, Castro CC, Bortolotto LA, Zerbibi MCN, Siqueira SAC, Toledo RA, Dahia PLM. Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation [Internet]. The Journal of clinical endocrinology and metabolism. 2015 ; 100( 2): E308-E318.[citado 2024 maio 15 ] Available from: http://press.endocrine.org/doi/pdf/10.1210/jc.2014-2473
Artigo de periodico-carta/editorial
RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma [Carta] (2015)
Toledo, Rodrigo A.; Maciel, Rui M. B.; Eric, Zoran; Lourenço Jr., Delmar M.; Cerutti, Janete M.; Eng, Charis; Neumann, Hartmut P.; Toledo, Sergio P.
Fonte: Thyroid. Unidade: FM
Assuntos: TIREOIDECTOMIA, DOENÇAS HEREDITÁRIAS, MUTAÇÃO GENÉTICA, CARCINOMA MEDULAR (GENÉTICA)
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ABNT
TOLEDO, Rodrigo A. et al. RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma [Carta]. Thyroid. New Rochelle: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1089/thy.2015.0168. Acesso em: 15 maio 2024. , 2015
APA
Toledo, R. A., Maciel, R. M. B., Eric, Z., Lourenço Jr., D. M., Cerutti, J. M., Eng, C., et al. (2015). RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma [Carta]. Thyroid. New Rochelle: Faculdade de Medicina, Universidade de São Paulo. doi:10.1089/thy.2015.0168
NLM
Toledo RA, Maciel RMB, Eric Z, Lourenço Jr. DM, Cerutti JM, Eng C, Neumann HP, Toledo SP. RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma [Carta] [Internet]. Thyroid. 2015 ; 25( 8): 973-974.[citado 2024 maio 15 ] Available from: https://doi.org/10.1089/thy.2015.0168
Vancouver
Toledo RA, Maciel RMB, Eric Z, Lourenço Jr. DM, Cerutti JM, Eng C, Neumann HP, Toledo SP. RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma [Carta] [Internet]. Thyroid. 2015 ; 25( 8): 973-974.[citado 2024 maio 15 ] Available from: https://doi.org/10.1089/thy.2015.0168
Artigo de periodico
Penetrance of functioning and nonfunctioning pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1 in the second decade of life (2014)
Gonçalves, Tatiana D.; Toledo, Rodrigo A.; Sekiya, Tomoko; Matuguma, Sergio E.; Maluf Filho, Fauze; Rocha, Manoel de Souza; Siqueira, Sheila A. C.; Glezer, Andrea; Bronstein, Marcelo D.; Pereira, Maria A. A.; Jureidini, Ricardo; Bacchella, Telesforo; Machado, Marcel Cerqueira César; Toledo, Sergio Pereira de Almeida; Lourenço Junior, Delmar M.
Fonte: The Journal of clinical endocrinology and metabolism. Unidade: FM
Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA, IMAGEM POR RESSONÂNCIA MAGNÉTICA, HIPOGLICEMIA
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ABNT
GONÇALVES, Tatiana D. et al. Penetrance of functioning and nonfunctioning pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1 in the second decade of life. The Journal of clinical endocrinology and metabolism, v. 99, n. 1, p. E89-E96, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-1768. Acesso em: 15 maio 2024.
APA
Gonçalves, T. D., Toledo, R. A., Sekiya, T., Matuguma, S. E., Maluf Filho, F., Rocha, M. de S., et al. (2014). Penetrance of functioning and nonfunctioning pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1 in the second decade of life. The Journal of clinical endocrinology and metabolism, 99( 1), E89-E96. doi:10.1210/jc.2013-1768
NLM
Gonçalves TD, Toledo RA, Sekiya T, Matuguma SE, Maluf Filho F, Rocha M de S, Siqueira SAC, Glezer A, Bronstein MD, Pereira MAA, Jureidini R, Bacchella T, Machado MCC, Toledo SP de A, Lourenço Junior DM. Penetrance of functioning and nonfunctioning pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1 in the second decade of life [Internet]. The Journal of clinical endocrinology and metabolism. 2014 ; 99( 1): E89-E96.[citado 2024 maio 15 ] Available from: https://doi.org/10.1210/jc.2013-1768
Vancouver
Gonçalves TD, Toledo RA, Sekiya T, Matuguma SE, Maluf Filho F, Rocha M de S, Siqueira SAC, Glezer A, Bronstein MD, Pereira MAA, Jureidini R, Bacchella T, Machado MCC, Toledo SP de A, Lourenço Junior DM. Penetrance of functioning and nonfunctioning pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1 in the second decade of life [Internet]. The Journal of clinical endocrinology and metabolism. 2014 ; 99( 1): E89-E96.[citado 2024 maio 15 ] Available from: https://doi.org/10.1210/jc.2013-1768
Artigo de periodico
Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study (2014)
Castinetti, Frederic; Qi, Xiao-Ping; Walz, Martin K.; Maia, Ana Luiza; Sansó, Gabriela; Peczkowska, Mariola; Hasse-Lazar, Kornelia; Links, Thera P.; Dvorakova, Sarka; Toledo, Rodrigo A.; Mian, Caterina; Bugalho, Maria Joao; Wohllk, Nelson; Kollyukh, Oleg; Canu, Letizia; Loli, Paola; Bergmann, Simona R.; Costa, Josefina Biarnes; Makay, Ozer; Patocs, Attila; Pfeifer, Marija; Shah, Nalini S.; Cuny, Thomas; Brauckhoff, Michael
Fonte: The Lancet Oncology. Unidade: FM
Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA (DIAGNÓSTICO;TERAPIA), CENTROS COMUNITÁRIOS DE SAÚDE, FEOCROMOCITOMA (EPIDEMIOLOGIA)
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ABNT
CASTINETTI, Frederic et al. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study. The Lancet Oncology, v. 15, n. 6, p. 648-655, 2014Tradução . . Disponível em: http://ac.els-cdn.com/S1470204514701548/1-s2.0-S1470204514701548-main.pdf?_tid=996753ea-2317-11e4-a1c7-00000aab0f6b&acdnat=1407954679_2dc799ef0beedd0ec92653f9a1263a3e. Acesso em: 15 maio 2024.
APA
Castinetti, F., Qi, X. -P., Walz, M. K., Maia, A. L., Sansó, G., Peczkowska, M., et al. (2014). Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study. The Lancet Oncology, 15( 6), 648-655. doi:10.1016/S1470-2045(14)70154-8
NLM
Castinetti F, Qi X-P, Walz MK, Maia AL, Sansó G, Peczkowska M, Hasse-Lazar K, Links TP, Dvorakova S, Toledo RA, Mian C, Bugalho MJ, Wohllk N, Kollyukh O, Canu L, Loli P, Bergmann SR, Costa JB, Makay O, Patocs A, Pfeifer M, Shah NS, Cuny T, Brauckhoff M. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study [Internet]. The Lancet Oncology. 2014 ; 15( 6): 648-655.[citado 2024 maio 15 ] Available from: http://ac.els-cdn.com/S1470204514701548/1-s2.0-S1470204514701548-main.pdf?_tid=996753ea-2317-11e4-a1c7-00000aab0f6b&acdnat=1407954679_2dc799ef0beedd0ec92653f9a1263a3e
Vancouver
Castinetti F, Qi X-P, Walz MK, Maia AL, Sansó G, Peczkowska M, Hasse-Lazar K, Links TP, Dvorakova S, Toledo RA, Mian C, Bugalho MJ, Wohllk N, Kollyukh O, Canu L, Loli P, Bergmann SR, Costa JB, Makay O, Patocs A, Pfeifer M, Shah NS, Cuny T, Brauckhoff M. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study [Internet]. The Lancet Oncology. 2014 ; 15( 6): 648-655.[citado 2024 maio 15 ] Available from: http://ac.els-cdn.com/S1470204514701548/1-s2.0-S1470204514701548-main.pdf?_tid=996753ea-2317-11e4-a1c7-00000aab0f6b&acdnat=1407954679_2dc799ef0beedd0ec92653f9a1263a3e
Artigo de periodico
Penetrance of TMEM127-related pheochromocytoma in a six-generation family (2014)
Toledo, S. P. A.; Lourenço Jr., D. M.; Sekiya, T.; Lucon, A. M.; Baena, R. C.; Castro, C. C.; Bortolotto, L. A.; Zerbini, M. C. N.; Siqueira, S. A. C.; Toledo, R. A.; Dahia, P. L. M.
Fonte: Wiener Klinische Wochenschrift. Nome do evento: International workshop on multiple endocrine neoplasia and other rare endocrine tumors. Unidade: FM
Assuntos: FEOCROMOCITOMA, MUTAÇÃO GENÉTICA, PROTEÍNAS DA MEMBRANA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEDO, S. P. A. et al. Penetrance of TMEM127-related pheochromocytoma in a six-generation family. Wiener Klinische Wochenschrift, v. 126, n. 3, p. S155, 2014Tradução . . Disponível em: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5. Acesso em: 15 maio 2024.
APA
Toledo, S. P. A., Lourenço Jr., D. M., Sekiya, T., Lucon, A. M., Baena, R. C., Castro, C. C., et al. (2014). Penetrance of TMEM127-related pheochromocytoma in a six-generation family. Wiener Klinische Wochenschrift, 126( 3), S155. Recuperado de http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
NLM
Toledo SPA, Lourenço Jr. DM, Sekiya T, Lucon AM, Baena RC, Castro CC, Bortolotto LA, Zerbini MCN, Siqueira SAC, Toledo RA, Dahia PLM. Penetrance of TMEM127-related pheochromocytoma in a six-generation family [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S155.[citado 2024 maio 15 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
Vancouver
Toledo SPA, Lourenço Jr. DM, Sekiya T, Lucon AM, Baena RC, Castro CC, Bortolotto LA, Zerbini MCN, Siqueira SAC, Toledo RA, Dahia PLM. Penetrance of TMEM127-related pheochromocytoma in a six-generation family [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S155.[citado 2024 maio 15 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
Artigo de periodico
Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations (2014)
Longuini, Viviane Cristina; Lourenço Júnior, Delmar M; Sekiya, Tomoko; Meirelles, Osorio; Goncalves, Tatiana D.; Coutinho, Flavia L.; Francisco, Guilherme; Osaki, Luciana H.; Chammas, Roger; Alves, Venâncio Avancini Ferreira; Siqueira, Sheila A. C.; Schlesinger, David; Naslavsky, Michel ; Zatz, Mayana ; Duarte, Yeda Aparecida de Oliveira ; Lebrão, Maria Lucia; Gama, Patrícia ; Lee, Misu; Molatore, Sara; Pereira, Maria Adelaide A.; Jallad, Raquel S.; Bronstein, Marcello D.; Cunha-Neto, Malebranche B.; Liberman, Bernardo; Fragoso, Maria Candida B. V.; Toledo, Sergio Pereira de Almeida; Pellegata, Natalia S.; Toledo, Rodrigo A.
Fonte: European Journal of Endocrinology. Unidades: FM, IB, EE, FSP, ICB
Assuntos: MUTAÇÃO GENÉTICA, GENÉTICA, NEOPLASIA ENDÓCRINA MÚLTIPLA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LONGUINI, Viviane Cristina et al. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European Journal of Endocrinology, n. Ju 2014, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-14-0130. Acesso em: 15 maio 2024.
APA
Longuini, V. C., Lourenço Júnior, D. M., Sekiya, T., Meirelles, O., Goncalves, T. D., Coutinho, F. L., et al. (2014). Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European Journal of Endocrinology, ( Ju 2014). doi:10.1530/EJE-14-0130
NLM
Longuini VC, Lourenço Júnior DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VAF, Siqueira SAC, Schlesinger D, Naslavsky M, Zatz M, Duarte YA de O, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MAA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo RA. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations [Internet]. European Journal of Endocrinology. 2014 ;( Ju 2014):[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/EJE-14-0130
Vancouver
Longuini VC, Lourenço Júnior DM, Sekiya T, Meirelles O, Goncalves TD, Coutinho FL, Francisco G, Osaki LH, Chammas R, Alves VAF, Siqueira SAC, Schlesinger D, Naslavsky M, Zatz M, Duarte YA de O, Lebrão ML, Gama P, Lee M, Molatore S, Pereira MAA, Jallad RS, Bronstein MD, Cunha-Neto MB, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo RA. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations [Internet]. European Journal of Endocrinology. 2014 ;( Ju 2014):[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/EJE-14-0130
Artigo de periodico
Lymph node distribution in the central compartment of the neck: An anatomic study (2014)
Tavares, Marcos Roberto; Cruz, José Arnaldo Shiomi da; Waisberg, Daniel Reis; Toledo, Sérgio Pereira de Almeida; Takeda, Flavio Roberto; Cernea, Claudio Roberto; Capelozzi, Vera Luiza; Brandão, Lenine Garcia
Fonte: Head & neck. Unidade: FM
Assuntos: LINFONODOS, PESCOÇO, NEOPLASIAS DA TIREOIDE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAVARES, Marcos Roberto et al. Lymph node distribution in the central compartment of the neck: An anatomic study. Head & neck, v. 36, n. 10, p. 1425-1430, 2014Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/hed.23469/pdf. Acesso em: 15 maio 2024.
APA
Tavares, M. R., Cruz, J. A. S. da, Waisberg, D. R., Toledo, S. P. de A., Takeda, F. R., Cernea, C. R., et al. (2014). Lymph node distribution in the central compartment of the neck: An anatomic study. Head & neck, 36( 10), 1425-1430. doi:10.1002/hed.23469
NLM
Tavares MR, Cruz JAS da, Waisberg DR, Toledo SP de A, Takeda FR, Cernea CR, Capelozzi VL, Brandão LG. Lymph node distribution in the central compartment of the neck: An anatomic study [Internet]. Head & neck. 2014 ; 36( 10): 1425-1430.[citado 2024 maio 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/hed.23469/pdf
Vancouver
Tavares MR, Cruz JAS da, Waisberg DR, Toledo SP de A, Takeda FR, Cernea CR, Capelozzi VL, Brandão LG. Lymph node distribution in the central compartment of the neck: An anatomic study [Internet]. Head & neck. 2014 ; 36( 10): 1425-1430.[citado 2024 maio 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/hed.23469/pdf
Artigo de periodico
Maxillary myxomas associated with MEN1 syndrome (2014)
Lourenço, D. M.; Toledo, R. A.; Sekiya, T.; Moraes, M. B.; Santana, L. S.; Toledo, S. P. A.
Fonte: Wiener Klinische Wochenschrift. Nome do evento: International workshop on multiple endocrine neoplasia and other rare endocrine tumors. Unidade: FM
Assuntos: GENES, OSSOS FACIAIS, NEOPLASIAS DO TECIDO CONJUNTIVO, MANDÍBULA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOURENÇO, D. M. et al. Maxillary myxomas associated with MEN1 syndrome. Wiener Klinische Wochenschrift, v. 126, n. 3, p. S142-S143, 2014Tradução . . Disponível em: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5. Acesso em: 15 maio 2024.
APA
Lourenço, D. M., Toledo, R. A., Sekiya, T., Moraes, M. B., Santana, L. S., & Toledo, S. P. A. (2014). Maxillary myxomas associated with MEN1 syndrome. Wiener Klinische Wochenschrift, 126( 3), S142-S143. Recuperado de http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
NLM
Lourenço DM, Toledo RA, Sekiya T, Moraes MB, Santana LS, Toledo SPA. Maxillary myxomas associated with MEN1 syndrome [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S142-S143.[citado 2024 maio 15 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
Vancouver
Lourenço DM, Toledo RA, Sekiya T, Moraes MB, Santana LS, Toledo SPA. Maxillary myxomas associated with MEN1 syndrome [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S142-S143.[citado 2024 maio 15 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
Artigo de periodico
p27 variant and corticotropinoma susceptibility: a genetic and in vitro study (2014)
Sekiya, Tomoko; Bronstein, Marcello Delano ; Benfini, Katiuscia; Longuini, Viviane Cristina; Jallad, Raquel Soares; Machado, Marcio Cardoso; Gonçalves, Tatiana Denk; Osaki, Luciana Harumi; Higashi, Leonardo; Viana Junior, Jose; Kater, Claudio; Lee, Misu; Molatore, Sara; Francisco, Guilherme; Chammas, Roger ; Naslavsky, Michel ; Schlesinger, David; Gama, Patrícia ; Duarte, Yeda Aparecida de Oliveira ; Lebrão, Maria Lúcia ; Zatz, Mayana ; Meirelles, Osorio; Liberman, Bernardo; Fragoso, Maria Candida Barisson Villares ; Toledo, Sergio Pereira de Almeida; Pellegata, Natalia S.; Toledo, Rodrigo de Almeida; Zatz, Mayana
Fonte: Endocrine-Related Cancer. Unidades: ICB, FM, EE, IB, FSP
Assuntos: BIOLOGIA CELULAR, GENÉTICA, MUTAÇÃO GENÉTICA, RATOS, POLIMORFISMO, GENÓTIPOS, NEOPLASIAS DA TIREOIDE, ADENOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SEKIYA, Tomoko et al. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study. Endocrine-Related Cancer, v. 21, n. 3, p. 395-404, 2014Tradução . . Disponível em: https://doi.org/10.1530/ERC-13-0486. Acesso em: 15 maio 2024.
APA
Sekiya, T., Bronstein, M. D., Benfini, K., Longuini, V. C., Jallad, R. S., Machado, M. C., et al. (2014). p27 variant and corticotropinoma susceptibility: a genetic and in vitro study. Endocrine-Related Cancer, 21( 3), 395-404. doi:10.1530/ERC-13-0486
NLM
Sekiya T, Bronstein MD, Benfini K, Longuini VC, Jallad RS, Machado MC, Gonçalves TD, Osaki LH, Higashi L, Viana Junior J, Kater C, Lee M, Molatore S, Francisco G, Chammas R, Naslavsky M, Schlesinger D, Gama P, Duarte YA de O, Lebrão ML, Zatz M, Meirelles O, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo R de A, Zatz M. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study [Internet]. Endocrine-Related Cancer. 2014 ; 21( 3): 395-404.[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/ERC-13-0486
Vancouver
Sekiya T, Bronstein MD, Benfini K, Longuini VC, Jallad RS, Machado MC, Gonçalves TD, Osaki LH, Higashi L, Viana Junior J, Kater C, Lee M, Molatore S, Francisco G, Chammas R, Naslavsky M, Schlesinger D, Gama P, Duarte YA de O, Lebrão ML, Zatz M, Meirelles O, Liberman B, Fragoso MCBV, Toledo SP de A, Pellegata NS, Toledo R de A, Zatz M. p27 variant and corticotropinoma susceptibility: a genetic and in vitro study [Internet]. Endocrine-Related Cancer. 2014 ; 21( 3): 395-404.[citado 2024 maio 15 ] Available from: https://doi.org/10.1530/ERC-13-0486
Artigo de periodico
Depression, anxiety, quality of life and psychological well-being in patients with multiple endocrine neoplasia type2 (2014)
Rodrigues, K. C.; Toledo, S. P. A.; Toledo, R. A.; Lourenço Jr., D. M.
Fonte: Wiener Klinische Wochenschrift. Nome do evento: International workshop on multiple endocrine neoplasia and other rare endocrine tumors. Unidade: FM
Assuntos: DEPRESSÃO, ANSIEDADE, NEOPLASIA ENDÓCRINA MÚLTIPLA, QUALIDADE DE VIDA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODRIGUES, K. C. et al. Depression, anxiety, quality of life and psychological well-being in patients with multiple endocrine neoplasia type2. Wiener Klinische Wochenschrift, v. 126, n. 3, p. S155, 2014Tradução . . Disponível em: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5. Acesso em: 15 maio 2024.
APA
Rodrigues, K. C., Toledo, S. P. A., Toledo, R. A., & Lourenço Jr., D. M. (2014). Depression, anxiety, quality of life and psychological well-being in patients with multiple endocrine neoplasia type2. Wiener Klinische Wochenschrift, 126( 3), S155. Recuperado de http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
NLM
Rodrigues KC, Toledo SPA, Toledo RA, Lourenço Jr. DM. Depression, anxiety, quality of life and psychological well-being in patients with multiple endocrine neoplasia type2 [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S155.[citado 2024 maio 15 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
Vancouver
Rodrigues KC, Toledo SPA, Toledo RA, Lourenço Jr. DM. Depression, anxiety, quality of life and psychological well-being in patients with multiple endocrine neoplasia type2 [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S155.[citado 2024 maio 15 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
Artigo de periodico
Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS (2013)
Agrawal, Nishant; Jiao, Yuchen; Sausen, Mark; Leary, Rebecca; Bettegowda, Chetan; Roberts, Nicholas J; Bhan, Sheetal; Ho, Allen S; Khan, Zubair; Bishop, Justin; Westra, William H; Wood, Laura D; Hruban, Ralph H; Tufano, Ralph P; Robinson, Bruce; Dralle, Henning; Toledo, Sergio Pereira Almeida; Toledo, Rodrigo A; Morris, Luc G T; Ghossein, Ronald A; Fagin, James A; Chan, Timothy A; Velculescu, Victor E; Vogelstein, Bert; Kinzler, Kenneth W; Papadopoulos, Nickolas; Nelkin, Barry D; Ball, Douglas W
Fonte: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Assuntos: NEOPLASIAS DA TIREOIDE (QUIMIOTERAPIA;RADIOTERAPIA), CARCINOMA MEDULAR, MUTAÇÃO GENÉTICA, SEQUENCIAMENTO GENÉTICO, DOENÇAS HEREDITÁRIAS, REAÇÃO EM CADEIA POR POLIMERASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AGRAWAL, Nishant et al. Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS. The Journal of Clinical Endocrinology & Metabolism, v. 98, n. 2, p. E364-E369, 2013Tradução . . Disponível em: https://doi.org/10.1210/jc.2012-2703. Acesso em: 15 maio 2024.
APA
Agrawal, N., Jiao, Y., Sausen, M., Leary, R., Bettegowda, C., Roberts, N. J., et al. (2013). Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS. The Journal of Clinical Endocrinology & Metabolism, 98( 2), E364-E369. doi:10.1210/jc.2012-2703
NLM
Agrawal N, Jiao Y, Sausen M, Leary R, Bettegowda C, Roberts NJ, Bhan S, Ho AS, Khan Z, Bishop J, Westra WH, Wood LD, Hruban RH, Tufano RP, Robinson B, Dralle H, Toledo SPA, Toledo RA, Morris LGT, Ghossein RA, Fagin JA, Chan TA, Velculescu VE, Vogelstein B, Kinzler KW, Papadopoulos N, Nelkin BD, Ball DW. Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS [Internet]. The Journal of Clinical Endocrinology & Metabolism. 2013 ; 98( 2): E364-E369.[citado 2024 maio 15 ] Available from: https://doi.org/10.1210/jc.2012-2703
Vancouver
Agrawal N, Jiao Y, Sausen M, Leary R, Bettegowda C, Roberts NJ, Bhan S, Ho AS, Khan Z, Bishop J, Westra WH, Wood LD, Hruban RH, Tufano RP, Robinson B, Dralle H, Toledo SPA, Toledo RA, Morris LGT, Ghossein RA, Fagin JA, Chan TA, Velculescu VE, Vogelstein B, Kinzler KW, Papadopoulos N, Nelkin BD, Ball DW. Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS [Internet]. The Journal of Clinical Endocrinology & Metabolism. 2013 ; 98( 2): E364-E369.[citado 2024 maio 15 ] Available from: https://doi.org/10.1210/jc.2012-2703
Artigo de periodico
A differential diagnosis of inherited endocrine tumors and their tumor counterparts (2013)
Toledo, Sergio Pereira de Almeida; Lourenço Junior, Delmar M; Toledo, Rodrigo A
Fonte: Clinics. Unidade: FM
Assuntos: DIAGNÓSTICO DIFERENCIAL, DOENÇAS HEREDITÁRIAS (DIAGNÓSTICO;TRANSMISSÃO), NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA), FATORES DE RISCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEDO, Sergio Pereira de Almeida e LOURENÇO JUNIOR, Delmar M e TOLEDO, Rodrigo A. A differential diagnosis of inherited endocrine tumors and their tumor counterparts. Clinics, v. 68, n. 7, p. 1039-1056, 2013Tradução . . Disponível em: https://doi.org/10.6061/clinics/2013(07)24. Acesso em: 15 maio 2024.
APA
Toledo, S. P. de A., Lourenço Junior, D. M., & Toledo, R. A. (2013). A differential diagnosis of inherited endocrine tumors and their tumor counterparts. Clinics, 68( 7), 1039-1056. doi:10.6061/clinics/2013(07)24
NLM
Toledo SP de A, Lourenço Junior DM, Toledo RA. A differential diagnosis of inherited endocrine tumors and their tumor counterparts [Internet]. Clinics. 2013 ; 68( 7): 1039-1056.[citado 2024 maio 15 ] Available from: https://doi.org/10.6061/clinics/2013(07)24
Vancouver
Toledo SP de A, Lourenço Junior DM, Toledo RA. A differential diagnosis of inherited endocrine tumors and their tumor counterparts [Internet]. Clinics. 2013 ; 68( 7): 1039-1056.[citado 2024 maio 15 ] Available from: https://doi.org/10.6061/clinics/2013(07)24
Artigo de periodico
Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation (2013)
Syro, Luis V.; Sundsbak, Jamie L.; Scheithauer, Bernd W.; Toledo, Rodrigo A.; Camargo, Mauricio; Heyer, Christina M.; Sekiya, Tomoko; Uribe, Humberto; Escobar, Jorge I.; Vasquez, Martin; Rotondo, Fabio; Toledo, Sergio P. A.; Kovacs, Kalman; Horvath, Eva; Babovic-Vuksanovic, Dusica; Harris, Peter C.
Fonte: Pituitary. Unidade: FM
Assuntos: NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, ADENOMA, ACROMEGALIA, CISTOS, RIM (PATOLOGIA), IMUNOHISTOQUÍMICA, POLIMORFISMO
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ABNT
SYRO, Luis V. et al. Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation. Pituitary, v. 15, n. 3, p. 342-349, 2013Tradução . . Disponível em: http://link.springer.com/article/10.1007/s11102-011-0325-0. Acesso em: 15 maio 2024.
APA
Syro, L. V., Sundsbak, J. L., Scheithauer, B. W., Toledo, R. A., Camargo, M., Heyer, C. M., et al. (2013). Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation. Pituitary, 15( 3), 342-349. doi:10.1007/s11102-011-0325-0
NLM
Syro LV, Sundsbak JL, Scheithauer BW, Toledo RA, Camargo M, Heyer CM, Sekiya T, Uribe H, Escobar JI, Vasquez M, Rotondo F, Toledo SPA, Kovacs K, Horvath E, Babovic-Vuksanovic D, Harris PC. Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation [Internet]. Pituitary. 2013 ; 15( 3): 342-349.[citado 2024 maio 15 ] Available from: http://link.springer.com/article/10.1007/s11102-011-0325-0
Vancouver
Syro LV, Sundsbak JL, Scheithauer BW, Toledo RA, Camargo M, Heyer CM, Sekiya T, Uribe H, Escobar JI, Vasquez M, Rotondo F, Toledo SPA, Kovacs K, Horvath E, Babovic-Vuksanovic D, Harris PC. Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation [Internet]. Pituitary. 2013 ; 15( 3): 342-349.[citado 2024 maio 15 ] Available from: http://link.springer.com/article/10.1007/s11102-011-0325-0

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