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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.
Source: Thyroid. Unidade: FM
Subjects: 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: 03 maio 2026. , 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 2026 maio 03 ] 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 2026 maio 03 ] Available from: https://doi.org/10.1089/thy.2015.0168
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 Junior, Delmar Muniz ; Lindsey, Susan C.; Camacho, Cleber Pinto ; Almeida, Marcio; Lima Junior, José V.; Sekiya, Tomoko; Garralda, Elena; Naslavsky, Michel ; Yamamoto, Guilherme L.; Lazar, Monize; Meirelles, Osorio; Sobreira, Tiago José Paschoal ; Lebrão, Maria Lúcia ; Duarte, Yeda Aparecida de Oliveira ; Blangero, John; Zatz, Mayana ; Cerutti, Janete Maria; Maciel, Rui Monteiro de Barros ; Toledo, Sergio Pereira de Almeida
Source: Endocrine - Related Cancer. Unidades: FSP, EE, IB, FM
Subjects: 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: 03 maio 2026.
APA
Toledo, R. A., Hatakana, R., Lourenço Junior, 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 Junior DM, Lindsey SC, Camacho CP, Almeida M, Lima Junior JV, Sekiya T, Garralda E, Naslavsky M, Yamamoto GL, Lazar M, Meirelles O, Sobreira TJP, Lebrão ML, Duarte YA de O, Blangero J, Zatz M, Cerutti JM, Maciel RM de B, Toledo SP de A. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility [Internet]. Endocrine - Related Cancer. 2015 ; 22( 2):[citado 2026 maio 03 ] Available from: https://doi.org/10.1530/ERC-14-0491
Vancouver
Toledo RA, Hatakana R, Lourenço Junior DM, Lindsey SC, Camacho CP, Almeida M, Lima Junior JV, Sekiya T, Garralda E, Naslavsky M, Yamamoto GL, Lazar M, Meirelles O, Sobreira TJP, Lebrão ML, Duarte YA de O, Blangero J, Zatz M, Cerutti JM, Maciel RM de B, Toledo SP de A. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility [Internet]. Endocrine - Related Cancer. 2015 ; 22( 2):[citado 2026 maio 03 ] Available from: https://doi.org/10.1530/ERC-14-0491
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.
Source: Archives of Endocrinology and Metabolism. Unidade: FM
Subjects: 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: 03 maio 2026. , 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 2026 maio 03 ] 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 2026 maio 03 ] Available from: https://doi.org/10.1590/2359-3997000000060
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.
Source: The Journal of clinical endocrinology and metabolism. Unidade: FM
Subjects: 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: 03 maio 2026.
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 2026 maio 03 ] 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 2026 maio 03 ] Available from: http://press.endocrine.org/doi/pdf/10.1210/jc.2014-2473
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 Denck; Toledo, Rodrigo A.; Sekiya, Tomoko; Matuguma, Sergio Eiji ; Maluf Filho, Fauze ; Rocha, Manoel de Souza ; Siqueira, Sheila Aparecida Coelho ; Glezer, Andrea ; Bronstein, Marcello Delano ; Pereira, Maria Adelaide Albergaria ; Jureidini, Ricardo; Bacchella, Telesforo; Machado, Marcel Cerqueira Cesar ; Toledo, Sergio Pereira de Almeida; Lourenço Junior, Delmar Muniz
Source: The Journal of clinical endocrinology and metabolism. Unidade: FM
Subjects: NEOPLASIA ENDÓCRINA MÚLTIPLA, IMAGEM POR RESSONÂNCIA MAGNÉTICA, HIPOGLICEMIA
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ABNT
GONÇALVES, Tatiana Denck 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: 03 maio 2026.
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 2026 maio 03 ] 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 2026 maio 03 ] 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
Source: The Lancet Oncology. Unidade: FM
Subjects: 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: 03 maio 2026.
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 2026 maio 03 ] 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 2026 maio 03 ] 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
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 Denck; 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.
Source: European Journal of Endocrinology. Unidades: FM, IB, EE, FSP, ICB
Subjects: MUTAÇÃO GENÉTICA, GENÉTICA, NEOPLASIA ENDÓCRINA MÚLTIPLA
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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: 03 maio 2026.
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 2026 maio 03 ] 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 2026 maio 03 ] Available from: https://doi.org/10.1530/EJE-14-0130
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.
Source: Pituitary. Unidade: FM
Subjects: 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: 03 maio 2026.
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 2026 maio 03 ] 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 2026 maio 03 ] Available from: http://link.springer.com/article/10.1007/s11102-011-0325-0
Artigo de periodico
Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 (2012)
Coutinho, Flavia L.; Lourenco Jr., Delmar M.; Toledo, Rodrigo A.; Montenegro, Fabio L. M.; Toledo, Sergio P. A.
Source: Clinics. Unidade: FM
Subjects: SEGUIMENTOS, NEOPLASIA ENDÓCRINA MÚLTIPLA (DIAGNÓSTICO), GLÂNDULAS PARATIREOIDES (FISIOPATOLOGIA), DENSIDADE ÓSSEA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COUTINHO, Flavia L. et al. Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1. Clinics, v. 67, p. 169-172, 2012Tradução . . Disponível em: https://doi.org/10.6061/clinics/2012(Sup01)28. Acesso em: 03 maio 2026.
APA
Coutinho, F. L., Lourenco Jr., D. M., Toledo, R. A., Montenegro, F. L. M., & Toledo, S. P. A. (2012). Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1. Clinics, 67, 169-172. doi:10.6061/clinics/2012(Sup01)28
NLM
Coutinho FL, Lourenco Jr. DM, Toledo RA, Montenegro FLM, Toledo SPA. Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 [Internet]. Clinics. 2012 ; 67 169-172.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)28
Vancouver
Coutinho FL, Lourenco Jr. DM, Toledo RA, Montenegro FLM, Toledo SPA. Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 [Internet]. Clinics. 2012 ; 67 169-172.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)28
Artigo de periodico
Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil (2012)
Toledo, Rodrigo A.; Sekiya, Tomoko; Longuini, Viviane C.; Coutinho, Flavia L.; Lourenço Jr., Delmar M.; Toledo, Sergio P. A.
Source: Clinics. Unidade: FM
Subjects: GENÔMICA, NEOPLASIA ENDÓCRINA MÚLTIPLA, GENÉTICA MÉDICA, PAÍSES EM DESENVOLVIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEDO, Rodrigo A. et al. Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil. Clinics, v. 67, p. 3-6, 2012Tradução . . Disponível em: https://doi.org/10.6061/clinics/2012(Sup01)02. Acesso em: 03 maio 2026.
APA
Toledo, R. A., Sekiya, T., Longuini, V. C., Coutinho, F. L., Lourenço Jr., D. M., & Toledo, S. P. A. (2012). Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil. Clinics, 67, 3-6. doi:10.6061/clinics/2012(Sup01)02
NLM
Toledo RA, Sekiya T, Longuini VC, Coutinho FL, Lourenço Jr. DM, Toledo SPA. Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil [Internet]. Clinics. 2012 ; 67 3-6.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)02
Vancouver
Toledo RA, Sekiya T, Longuini VC, Coutinho FL, Lourenço Jr. DM, Toledo SPA. Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil [Internet]. Clinics. 2012 ; 67 3-6.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)02
Artigo de periodico
RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family (2012)
Quedas, Elisangela P. S.; Toledo, Rodrigo A.; Longuini, Viviane C.; Sekiya, Tomoko; Coutinho, Flavia L.; Toledo, Sergio P. A.; Tannuri, Uenis
Source: Clinics. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA), DOENÇAS GENÉTICAS, CARCINOMA, MEGACOLON (GENÉTICA), NEOPLASIAS DA TIREOIDE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QUEDAS, Elisangela P. S. et al. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family. Clinics, v. 67, p. 57-61, 2012Tradução . . Disponível em: https://doi.org/10.6061/clinics/2012(Sup01)11. Acesso em: 03 maio 2026.
APA
Quedas, E. P. S., Toledo, R. A., Longuini, V. C., Sekiya, T., Coutinho, F. L., Toledo, S. P. A., & Tannuri, U. (2012). RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family. Clinics, 67, 57-61. doi:10.6061/clinics/2012(Sup01)11
NLM
Quedas EPS, Toledo RA, Longuini VC, Sekiya T, Coutinho FL, Toledo SPA, Tannuri U. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family [Internet]. Clinics. 2012 ; 67 57-61.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)11
Vancouver
Quedas EPS, Toledo RA, Longuini VC, Sekiya T, Coutinho FL, Toledo SPA, Tannuri U. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family [Internet]. Clinics. 2012 ; 67 57-61.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)11
Artigo de periodico
Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1 (2012)
Lourenço Jr., Delmar M.; Coutinho, Flavia L.; Toledo, Rodrigo A.; Gonçalves, Tatiana Denck; Montenegro, Fabio L. M.; Toledo, Sergio P. A.
Source: Clinics. Unidade: FM
Subjects: OSSO E OSSOS (FISIOPATOLOGIA), NEOPLASIA ENDÓCRINA MÚLTIPLA (PATOLOGIA), RIM (FISIOPATOLOGIA), NEFROPATIAS (PATOLOGIA), GLÂNDULAS PARATIREOIDES (PATOLOGIA), HISTÓRIA NATURAL, DESMINERALIZAÇÃO, BIOQUÍMICA CLÍNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOURENÇO JR., Delmar M. et al. Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1. Clinics, v. 67, n. supl.1, p. 99-108, 2012Tradução . . Disponível em: https://doi.org/10.6061/clinics/2012(Sup01)17. Acesso em: 03 maio 2026.
APA
Lourenço Jr., D. M., Coutinho, F. L., Toledo, R. A., Gonçalves, T. D., Montenegro, F. L. M., & Toledo, S. P. A. (2012). Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1. Clinics, 67( supl.1), 99-108. doi:10.6061/clinics/2012(Sup01)17
NLM
Lourenço Jr. DM, Coutinho FL, Toledo RA, Gonçalves TD, Montenegro FLM, Toledo SPA. Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1 [Internet]. Clinics. 2012 ; 67( supl.1): 99-108.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)17
Vancouver
Lourenço Jr. DM, Coutinho FL, Toledo RA, Gonçalves TD, Montenegro FLM, Toledo SPA. Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1 [Internet]. Clinics. 2012 ; 67( supl.1): 99-108.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)17
Artigo de periodico
Growth hormone response to growth hormone-releasing peptide-2 in growth hormone-deficient Little mice (2012)
Peroni, Cibele N.; Hayashida, Cesar Y.; Nascimento, Nancy; Longuini, Viviane C.; Toledo, Rodrigo A.; Bartolini, Paolo; Bowers, Cyril Y.; Toledo, Sergio P. A.
Source: Clinics. Unidade: FM
Subjects: LEPTINA (ANÁLISE;NÍVEL), CAMUNDONGOS, MODELOS ANIMAIS, FENÓTIPOS, ANÁLISE SEQUENCIAL, GENÓTIPOS, MUTAÇÃO GENÉTICA, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PERONI, Cibele N. et al. Growth hormone response to growth hormone-releasing peptide-2 in growth hormone-deficient Little mice. Clinics, v. 67, n. 3, p. 265-272, 2012Tradução . . Disponível em: https://doi.org/10.6061/clinics/2012(03)11. Acesso em: 03 maio 2026.
APA
Peroni, C. N., Hayashida, C. Y., Nascimento, N., Longuini, V. C., Toledo, R. A., Bartolini, P., et al. (2012). Growth hormone response to growth hormone-releasing peptide-2 in growth hormone-deficient Little mice. Clinics, 67( 3), 265-272. doi:10.6061/clinics/2012(03)11
NLM
Peroni CN, Hayashida CY, Nascimento N, Longuini VC, Toledo RA, Bartolini P, Bowers CY, Toledo SPA. Growth hormone response to growth hormone-releasing peptide-2 in growth hormone-deficient Little mice [Internet]. Clinics. 2012 ; 67( 3): 265-272.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(03)11
Vancouver
Peroni CN, Hayashida CY, Nascimento N, Longuini VC, Toledo RA, Bartolini P, Bowers CY, Toledo SPA. Growth hormone response to growth hormone-releasing peptide-2 in growth hormone-deficient Little mice [Internet]. Clinics. 2012 ; 67( 3): 265-272.[citado 2026 maio 03 ] Available from: https://doi.org/10.6061/clinics/2012(03)11
Artigo de periodico
Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 (2011)
Frank-Raue, Karin; Rybicki, Lisa A.; Erlic, Zoran; Schweizer, Heiko; Winter, Aurelia; Milos, Ioana; Toledo, Sergio Pereira de Almeida; Toledo, Rodrigo A.; Tavares, Marcos R.; Alevizaki, Maria; Mian, Caterina; Siggelkow, Heide; Hüfner, Michael; Wohllk, Nelson; Opocher, Giuseppe; Dvořáková, Šárka; Bendlova, Bela; Czetwertynska, Małgorzata; Skasko, Elżbieta; Barontini, Marta; Sanso, Gabriela; Vorländer, Christian; Maia, Ana Luiza; Patocs, Attila; Links, Thera P.; de Groot, Jan Willem; Kerstens, Michiel N.; Valk, Gerlof D.; Miehle, Konstanze; Musholt, Thomas J.; Biarnes, Josefina; Damjanovic, Svetozar; Muresan, Mihaela; Wüster, Christian; Fassnacht, Martin; Peczkowska, Mariola; Fauth, Christine; Golcher, Henriette; Walter, Martin A.; Pichl, Josef; Raue, Friedhelm; Eng, Charis; Neumann, Hartmut P. H.
Source: Human mutation. Unidade: FM
Subjects: NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA), FATORES DE CRESCIMENTO, NEOPLASIAS DA TIREOIDE, GENÓTIPOS, CARCINOMA MEDULAR, FENÓTIPOS, METÁSTASE NEOPLÁSICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANK-RAUE, Karin et al. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, v. 32, n. 1, p. 51-58, 2011Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf. Acesso em: 03 maio 2026.
APA
Frank-Raue, K., Rybicki, L. A., Erlic, Z., Schweizer, H., Winter, A., Milos, I., et al. (2011). Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, 32( 1), 51-58. doi:10.1002/humu.21385
NLM
Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP de A, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková Š, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HPH. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 [Internet]. Human mutation. 2011 ; 32( 1): 51-58.[citado 2026 maio 03 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf
Vancouver
Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP de A, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková Š, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HPH. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 [Internet]. Human mutation. 2011 ; 32( 1): 51-58.[citado 2026 maio 03 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf
Artigo de periodico
High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene (2010)
Toledo, Rodrigo A.; Wagner, Simona M.; Coutinho, Flavia L.; Lourenço Jr., Delmar M.; Azevedo, Juliana A.; Longuini, Viviane C.; Reis, Mariana T. A.; Siqueira, Sheila A. C.; Lucon, Antonio Marmo; Tavares, Marcos R.; Fragoso, Maria C. B. V.; Pereira, Adelaide A.; Dahia, Patricia L. M.; Mulligan, Lois M.; Toledo, Sérgio P. A.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: FEOCROMOCITOMA, PROTO-ONCOGENES, NEOPLASIA ENDÓCRINA MÚLTIPLA, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEDO, Rodrigo A. et al. High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 3, p. 1318-1327, 2010Tradução . . Disponível em: http://jcem.endojournals.org/cgi/reprint/95/3/1318. Acesso em: 03 maio 2026.
APA
Toledo, R. A., Wagner, S. M., Coutinho, F. L., Lourenço Jr., D. M., Azevedo, J. A., Longuini, V. C., et al. (2010). High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene. Journal of Clinical Endocrinology and Metabolism, 95( 3), 1318-1327. Recuperado de http://jcem.endojournals.org/cgi/reprint/95/3/1318
NLM
Toledo RA, Wagner SM, Coutinho FL, Lourenço Jr. DM, Azevedo JA, Longuini VC, Reis MTA, Siqueira SAC, Lucon AM, Tavares MR, Fragoso MCBV, Pereira AA, Dahia PLM, Mulligan LM, Toledo SPA. High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 3): 1318-1327.[citado 2026 maio 03 ] Available from: http://jcem.endojournals.org/cgi/reprint/95/3/1318
Vancouver
Toledo RA, Wagner SM, Coutinho FL, Lourenço Jr. DM, Azevedo JA, Longuini VC, Reis MTA, Siqueira SAC, Lucon AM, Tavares MR, Fragoso MCBV, Pereira AA, Dahia PLM, Mulligan LM, Toledo SPA. High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 3): 1318-1327.[citado 2026 maio 03 ] Available from: http://jcem.endojournals.org/cgi/reprint/95/3/1318
Artigo de periodico
Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy (2010)
Coutinho, Flavia L.; Lourenço Jr., Delmar M.; Toledo, Rodrigo A.; Montenegro, Fabio L. M.; Correia-Deur, Joya E. M.; Toledo, Sergio P. A.
Source: Clinical Endocrinology. Unidade: FM
Subjects: DENSIDADE ÓSSEA, NEOPLASIA ENDÓCRINA MÚLTIPLA, PARATIREOIDECTOMIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COUTINHO, Flavia L. et al. Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy. Clinical Endocrinology, v. 72, n. 4, p. 462-468, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2009.03672.x. Acesso em: 03 maio 2026.
APA
Coutinho, F. L., Lourenço Jr., D. M., Toledo, R. A., Montenegro, F. L. M., Correia-Deur, J. E. M., & Toledo, S. P. A. (2010). Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy. Clinical Endocrinology, 72( 4), 462-468. doi:10.1111/j.1365-2265.2009.03672.x
NLM
Coutinho FL, Lourenço Jr. DM, Toledo RA, Montenegro FLM, Correia-Deur JEM, Toledo SPA. Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy [Internet]. Clinical Endocrinology. 2010 ; 72( 4): 462-468.[citado 2026 maio 03 ] Available from: https://doi.org/10.1111/j.1365-2265.2009.03672.x
Vancouver
Coutinho FL, Lourenço Jr. DM, Toledo RA, Montenegro FLM, Correia-Deur JEM, Toledo SPA. Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy [Internet]. Clinical Endocrinology. 2010 ; 72( 4): 462-468.[citado 2026 maio 03 ] Available from: https://doi.org/10.1111/j.1365-2265.2009.03672.x
Artigo de periodico
Early-Onset, Progressive, Frequent, Extensive, and Severe Bone Mineral and Renal Complications in Multiple Endocrine Neoplasia Type 1–Associated Primary Hyperparathyroidism (2010)
Lourenço Jr., Delmar M.; Coutinho, Flavia L.; Toledo, Rodrigo A.; Montenegro, Fabio L. M.; Correia-Deur, Joya E. M.; Toledo, Sergio P. A.
Source: Journal of Bone and Mineral Research. Unidade: FM
Subjects: DENSIDADE ÓSSEA, NEFROPATIAS, GLÂNDULAS PARATIREOIDES (FISIOPATOLOGIA), NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOURENÇO JR., Delmar M. et al. Early-Onset, Progressive, Frequent, Extensive, and Severe Bone Mineral and Renal Complications in Multiple Endocrine Neoplasia Type 1–Associated Primary Hyperparathyroidism. Journal of Bone and Mineral Research, v. 25, n. 11, p. 2382-2391, 2010Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/jbmr.125/pdf. Acesso em: 03 maio 2026.
APA
Lourenço Jr., D. M., Coutinho, F. L., Toledo, R. A., Montenegro, F. L. M., Correia-Deur, J. E. M., & Toledo, S. P. A. (2010). Early-Onset, Progressive, Frequent, Extensive, and Severe Bone Mineral and Renal Complications in Multiple Endocrine Neoplasia Type 1–Associated Primary Hyperparathyroidism. Journal of Bone and Mineral Research, 25( 11), 2382-2391. doi:10.1002/jbmr.125
NLM
Lourenço Jr. DM, Coutinho FL, Toledo RA, Montenegro FLM, Correia-Deur JEM, Toledo SPA. Early-Onset, Progressive, Frequent, Extensive, and Severe Bone Mineral and Renal Complications in Multiple Endocrine Neoplasia Type 1–Associated Primary Hyperparathyroidism [Internet]. Journal of Bone and Mineral Research. 2010 ;25( 11): 2382-2391.[citado 2026 maio 03 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/jbmr.125/pdf
Vancouver
Lourenço Jr. DM, Coutinho FL, Toledo RA, Montenegro FLM, Correia-Deur JEM, Toledo SPA. Early-Onset, Progressive, Frequent, Extensive, and Severe Bone Mineral and Renal Complications in Multiple Endocrine Neoplasia Type 1–Associated Primary Hyperparathyroidism [Internet]. Journal of Bone and Mineral Research. 2010 ;25( 11): 2382-2391.[citado 2026 maio 03 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/jbmr.125/pdf
Artigo de periodico
Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study (2010)
Daly, Adrian F.; Tichomirowa, Maria A.; Petrossians, Patrick; Heliövaara, Elina; Jaffrain-Rea, Marie-Lise; Barlier, Anne; Naves, Luciana A.; Ebeling, Tapani; Karhu, Auli; Raappana, Antti; Cazabat, Laure; De Menis, Ernesto; Montañana, Carmen Fajardo; Raverot, Gerald; Weil, Robert J.; Sane, Timo; Maiter, Dominique; Neggers, Sebastian; Yaneva, Maria; Tabarin, AntoineAntoine; Verrua, Elisa; Eloranta, Eija; Murat, Arnaud; Vierimaa, Outi; Salmela, Pasi I.; Emy, Philippe; Toledo, Rodrigo A.; Sabaté , Maria Isabel; Villa, Chiara; Popelier, Marc; Salvatori, Roberto; Jennings, Juliet; Longás, Ángel Ferrandez; Aizpún, José Ignacio Labarta; Georgitsi, Marianthi; Paschke, Ralf; Ronchi, Cristina; Valimaki, Matti; Saloranta, Carola; De Herder, Wouter; Cozzi, Renato; Guitelman, Mirtha; Magri, Flavia; Lagonigro, Maria Stefania; Halaby, Georges; Corman, Vinciane; Hagelstein, Marie-Thérèse; Vanbellinghen, Jean-Francis; Barra, Gustavo Barcelos; Gimenez-Roqueplo, Anne-Paule; Cameron, Fergus J.; Borson-Chazot, Francoise; Holdaway, Ian; Toledo, Sergio P. A.; Stalla, Gunter K.; Spada, Anna; Zacharieva, Sabina; Bertherat, Jerome; Brue, Thierry; Bours, Vincent; Chanson, Philippe; Aaltonen, Lauri A.; Beckers, Albert
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, ESTUDOS RETROSPECTIVOS, GLÂNDULA PRITUITÁRIA (PATOLOGIA), ADENOMAS (PATOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DALY, Adrian F. et al. Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 11, p. E373-E383, 2010Tradução . . Disponível em: https://doi.org/10.1210/jc.2009-2556. Acesso em: 03 maio 2026.
APA
Daly, A. F., Tichomirowa, M. A., Petrossians, P., Heliövaara, E., Jaffrain-Rea, M. -L., Barlier, A., et al. (2010). Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study. Journal of Clinical Endocrinology and Metabolism, 95( 11), E373-E383. doi:10.1210/jc.2009-2556
NLM
Daly AF, Tichomirowa MA, Petrossians P, Heliövaara E, Jaffrain-Rea M-L, Barlier A, Naves LA, Ebeling T, Karhu A, Raappana A, Cazabat L, De Menis E, Montañana CF, Raverot G, Weil RJ, Sane T, Maiter D, Neggers S, Yaneva M, Tabarin AA, Verrua E, Eloranta E, Murat A, Vierimaa O, Salmela PI, Emy P, Toledo RA, Sabaté MI, Villa C, Popelier M, Salvatori R, Jennings J, Longás ÁF, Aizpún JIL, Georgitsi M, Paschke R, Ronchi C, Valimaki M, Saloranta C, De Herder W, Cozzi R, Guitelman M, Magri F, Lagonigro MS, Halaby G, Corman V, Hagelstein M-T, Vanbellinghen J-F, Barra GB, Gimenez-Roqueplo A-P, Cameron FJ, Borson-Chazot F, Holdaway I, Toledo SPA, Stalla GK, Spada A, Zacharieva S, Bertherat J, Brue T, Bours V, Chanson P, Aaltonen LA, Beckers A. Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 11): E373-E383.[citado 2026 maio 03 ] Available from: https://doi.org/10.1210/jc.2009-2556
Vancouver
Daly AF, Tichomirowa MA, Petrossians P, Heliövaara E, Jaffrain-Rea M-L, Barlier A, Naves LA, Ebeling T, Karhu A, Raappana A, Cazabat L, De Menis E, Montañana CF, Raverot G, Weil RJ, Sane T, Maiter D, Neggers S, Yaneva M, Tabarin AA, Verrua E, Eloranta E, Murat A, Vierimaa O, Salmela PI, Emy P, Toledo RA, Sabaté MI, Villa C, Popelier M, Salvatori R, Jennings J, Longás ÁF, Aizpún JIL, Georgitsi M, Paschke R, Ronchi C, Valimaki M, Saloranta C, De Herder W, Cozzi R, Guitelman M, Magri F, Lagonigro MS, Halaby G, Corman V, Hagelstein M-T, Vanbellinghen J-F, Barra GB, Gimenez-Roqueplo A-P, Cameron FJ, Borson-Chazot F, Holdaway I, Toledo SPA, Stalla GK, Spada A, Zacharieva S, Bertherat J, Brue T, Bours V, Chanson P, Aaltonen LA, Beckers A. Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 11): E373-E383.[citado 2026 maio 03 ] Available from: https://doi.org/10.1210/jc.2009-2556
Artigo de periodico
Isolated familial somatotropinoma: 11Q13-LOH and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis (2010)
Toledo, Rodrigo A.; Mendonca, Berenice Bilharinho de ; Fragoso, Maria Candida Barisson Villares ; Soares, Iberê Cauduro; Almeida, Madson Queiroz de; Moraes, Michelle Buscarilli de; Lourenço Junior, Delmar Muniz ; Alves, Venancio Avancini Ferreira ; Bronstein, Marcello Delano ; Toledo, Sergio Pereira de Almeida
Source: Clinics. Unidade: FM
Subjects: PROTEÍNAS, GLÂNDULA PITUITÁRIA (PATOLOGIA), ACROMEGALIA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEDO, Rodrigo A. et al. Isolated familial somatotropinoma: 11Q13-LOH and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis. Clinics, v. 65, n. 4, p. 407-415, 2010Tradução . . Disponível em: https://doi.org/10.1590/s1807-59322010000400010. Acesso em: 03 maio 2026.
APA
Toledo, R. A., Mendonca, B. B. de, Fragoso, M. C. B. V., Soares, I. C., Almeida, M. Q. de, Moraes, M. B. de, et al. (2010). Isolated familial somatotropinoma: 11Q13-LOH and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis. Clinics, 65( 4), 407-415. doi:10.1590/s1807-59322010000400010
NLM
Toledo RA, Mendonca BB de, Fragoso MCBV, Soares IC, Almeida MQ de, Moraes MB de, Lourenço Junior DM, Alves VAF, Bronstein MD, Toledo SP de A. Isolated familial somatotropinoma: 11Q13-LOH and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis [Internet]. Clinics. 2010 ; 65( 4): 407-415.[citado 2026 maio 03 ] Available from: https://doi.org/10.1590/s1807-59322010000400010
Vancouver
Toledo RA, Mendonca BB de, Fragoso MCBV, Soares IC, Almeida MQ de, Moraes MB de, Lourenço Junior DM, Alves VAF, Bronstein MD, Toledo SP de A. Isolated familial somatotropinoma: 11Q13-LOH and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis [Internet]. Clinics. 2010 ; 65( 4): 407-415.[citado 2026 maio 03 ] Available from: https://doi.org/10.1590/s1807-59322010000400010
Artigo de periodico-carta/editorial
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma [Carta] (2010)
Qin, Yuejuan; Yao, Li; King, Elizabeth E.; Buddavarapu, Kalyan; Lenci, Romina E.; Chocron, E. Sandra; Lechleiter, James D.; Sass, Meghan; Aronin, Neil; Schiavi, Francesca; Boaretto, Francesca; Opocher, Giuseppe; Toledo, Rodrigo A.; Toledo, Sergio P. A.; Stiles, Charles; Aguiar, Ricardo C. T.; Dahia, Patricia L. M.
Source: Nature genetics. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, FEOCROMOCITOMA (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QIN, Yuejuan et al. Germline mutations in TMEM127 confer susceptibility to pheochromocytoma [Carta]. Nature genetics. New York: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://www.nature.com/ng/journal/v42/n3/index.html. Acesso em: 03 maio 2026. , 2010
APA
Qin, Y., Yao, L., King, E. E., Buddavarapu, K., Lenci, R. E., Chocron, E. S., et al. (2010). Germline mutations in TMEM127 confer susceptibility to pheochromocytoma [Carta]. Nature genetics. New York: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://www.nature.com/ng/journal/v42/n3/index.html
NLM
Qin Y, Yao L, King EE, Buddavarapu K, Lenci RE, Chocron ES, Lechleiter JD, Sass M, Aronin N, Schiavi F, Boaretto F, Opocher G, Toledo RA, Toledo SPA, Stiles C, Aguiar RCT, Dahia PLM. Germline mutations in TMEM127 confer susceptibility to pheochromocytoma [Carta] [Internet]. Nature genetics. 2010 ; 42( 3): 229-233.[citado 2026 maio 03 ] Available from: http://www.nature.com/ng/journal/v42/n3/index.html
Vancouver
Qin Y, Yao L, King EE, Buddavarapu K, Lenci RE, Chocron ES, Lechleiter JD, Sass M, Aronin N, Schiavi F, Boaretto F, Opocher G, Toledo RA, Toledo SPA, Stiles C, Aguiar RCT, Dahia PLM. Germline mutations in TMEM127 confer susceptibility to pheochromocytoma [Carta] [Internet]. Nature genetics. 2010 ; 42( 3): 229-233.[citado 2026 maio 03 ] Available from: http://www.nature.com/ng/journal/v42/n3/index.html

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