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Artigo de periodico
Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years (2015)
Fragoso, Yara Dadalti; Alves-Leon, Soniza Vieira; Barreira, Amilton Antunes; Callegaro, Dagoberto; Ferreira, Maria Lucia Brito; Finkelsztejn, Alessandro; Gomes, Sidney; Gonçalves, Marcus Vinicius Magno; Machado, Maria Iris Moraes; Marques, Vanessa Daccach; Matta, Andre Palma Cunha; Papais-Alvarenga, Regina Maria; Pereira, Samira Luisa Apostolos; Tauil, Carlos Bernardo
Source: Pediatric Neurology. Unidade: FMRP
Subjects: ESCLEROSE MÚLTIPLA, CRIANÇAS, ADOLESCENTES, FÁRMACOS IMUNOSSUPRESSORES
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ABNT
FRAGOSO, Yara Dadalti et al. Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years. Pediatric Neurology, v. 53, n. 2, p. 166-168, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2015.03.024. Acesso em: 17 nov. 2024.
APA
Fragoso, Y. D., Alves-Leon, S. V., Barreira, A. A., Callegaro, D., Ferreira, M. L. B., Finkelsztejn, A., et al. (2015). Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years. Pediatric Neurology, 53( 2), 166-168. doi:10.1016/j.pediatrneurol.2015.03.024
NLM
Fragoso YD, Alves-Leon SV, Barreira AA, Callegaro D, Ferreira MLB, Finkelsztejn A, Gomes S, Gonçalves MVM, Machado MIM, Marques VD, Matta APC, Papais-Alvarenga RM, Pereira SLA, Tauil CB. Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years [Internet]. Pediatric Neurology. 2015 ; 53( 2): 166-168.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2015.03.024
Vancouver
Fragoso YD, Alves-Leon SV, Barreira AA, Callegaro D, Ferreira MLB, Finkelsztejn A, Gomes S, Gonçalves MVM, Machado MIM, Marques VD, Matta APC, Papais-Alvarenga RM, Pereira SLA, Tauil CB. Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years [Internet]. Pediatric Neurology. 2015 ; 53( 2): 166-168.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2015.03.024
Artigo de periodico
Long-term effects of exposure to disease-modifying drugs in the offspring of mothers with multiple sclerosis: a retrospective chart review (2013)
Fragoso, Yara D.; Adoni, Tarso; Alves-Leon, Soniza V.; Azambuja Jr, Nério D.; Barreira, Amilton Antunes; Brooks, Joseph B. B.; Carneiro, Denise S. D.; Carvalho, Margarete J.; Claudino, Rinaldo; Comini-Frota, Elizabeth R.; Domingues, Renan B.; Finkelzstejn, Alessandro; Gama, Paulo D.; Giacomo, Maria C. B.; Gomes, Sidney; Goncalves, Marcus V. M.; Grzesiuk, Anderson K.; Kaimen-Maciel, Damacio R.; Mendes, Maria F.; Morales, Nivea M. O.; Morales, Rogério R.; Muniz, Andre; Papais-Alvarenga, Regina M.; Parolin, Monica K. F.; Ribeiro, Sonia B. F.; Ruocco, Heloisa H.; Siquineli, Fabio; Tosta, Elza D.
Source: CNS Drugs. Unidade: FMRP
Subjects: TEMPO, EXPOSIÇÃO MATERNA, ESCLEROSE MÚLTIPLA, GRAVIDEZ, FETO, FÁRMACOS
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ABNT
FRAGOSO, Yara D. et al. Long-term effects of exposure to disease-modifying drugs in the offspring of mothers with multiple sclerosis: a retrospective chart review. CNS Drugs, v. 27, n. 11, p. 955-961, 2013Tradução . . Disponível em: https://doi.org/10.1007/s40263-013-0113-7. Acesso em: 17 nov. 2024.
APA
Fragoso, Y. D., Adoni, T., Alves-Leon, S. V., Azambuja Jr, N. D., Barreira, A. A., Brooks, J. B. B., et al. (2013). Long-term effects of exposure to disease-modifying drugs in the offspring of mothers with multiple sclerosis: a retrospective chart review. CNS Drugs, 27( 11), 955-961. doi:10.1007/s40263-013-0113-7
NLM
Fragoso YD, Adoni T, Alves-Leon SV, Azambuja Jr ND, Barreira AA, Brooks JBB, Carneiro DSD, Carvalho MJ, Claudino R, Comini-Frota ER, Domingues RB, Finkelzstejn A, Gama PD, Giacomo MCB, Gomes S, Goncalves MVM, Grzesiuk AK, Kaimen-Maciel DR, Mendes MF, Morales NMO, Morales RR, Muniz A, Papais-Alvarenga RM, Parolin MKF, Ribeiro SBF, Ruocco HH, Siquineli F, Tosta ED. Long-term effects of exposure to disease-modifying drugs in the offspring of mothers with multiple sclerosis: a retrospective chart review [Internet]. CNS Drugs. 2013 ; 27( 11): 955-961.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s40263-013-0113-7
Vancouver
Fragoso YD, Adoni T, Alves-Leon SV, Azambuja Jr ND, Barreira AA, Brooks JBB, Carneiro DSD, Carvalho MJ, Claudino R, Comini-Frota ER, Domingues RB, Finkelzstejn A, Gama PD, Giacomo MCB, Gomes S, Goncalves MVM, Grzesiuk AK, Kaimen-Maciel DR, Mendes MF, Morales NMO, Morales RR, Muniz A, Papais-Alvarenga RM, Parolin MKF, Ribeiro SBF, Ruocco HH, Siquineli F, Tosta ED. Long-term effects of exposure to disease-modifying drugs in the offspring of mothers with multiple sclerosis: a retrospective chart review [Internet]. CNS Drugs. 2013 ; 27( 11): 955-961.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s40263-013-0113-7
Artigo de periodico
Frequency of reported European ancestry among multiple sclerosis patients from four cities in the southern and southeastern regions of Brazil (2013)
Comini-Frota, Elizabeth Regina; Brum, Doralina Guimarães; Kaimen-Maciel, Damacio Ramon; Fragoso, Yara Dadalti; Barreira, Amilton Antunes; Donadi, Eduardo Antônio
Source: Clinical Neurology and Neurosurgery. Unidade: FMRP
Subjects: ESCLEROSE MÚLTIPLA, BRASILEIROS (EPIDEMIOLOGIA), IMIGRAÇÃO
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ABNT
COMINI-FROTA, Elizabeth Regina et al. Frequency of reported European ancestry among multiple sclerosis patients from four cities in the southern and southeastern regions of Brazil. Clinical Neurology and Neurosurgery, v. 115, n. 9, p. 1642-1646, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.clineuro.2013.02.024. Acesso em: 17 nov. 2024.
APA
Comini-Frota, E. R., Brum, D. G., Kaimen-Maciel, D. R., Fragoso, Y. D., Barreira, A. A., & Donadi, E. A. (2013). Frequency of reported European ancestry among multiple sclerosis patients from four cities in the southern and southeastern regions of Brazil. Clinical Neurology and Neurosurgery, 115( 9), 1642-1646. doi:10.1016/j.clineuro.2013.02.024
NLM
Comini-Frota ER, Brum DG, Kaimen-Maciel DR, Fragoso YD, Barreira AA, Donadi EA. Frequency of reported European ancestry among multiple sclerosis patients from four cities in the southern and southeastern regions of Brazil [Internet]. Clinical Neurology and Neurosurgery. 2013 ; 115( 9): 1642-1646.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.clineuro.2013.02.024
Vancouver
Comini-Frota ER, Brum DG, Kaimen-Maciel DR, Fragoso YD, Barreira AA, Donadi EA. Frequency of reported European ancestry among multiple sclerosis patients from four cities in the southern and southeastern regions of Brazil [Internet]. Clinical Neurology and Neurosurgery. 2013 ; 115( 9): 1642-1646.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.clineuro.2013.02.024
Artigo de periodico
Expanding the differencial diagnosis of inherited neuropathies with non-uniform conduction: andermann syndrome (2012)
Lourenço, Charles M.; Dupré, Nicolas; Rivière, Jean-Baptiste; Rouleau, Guy A.; Marques, Vanessa D.; Genari, Adriana B.; Santos, Antônio Carlos dos; Barreira, Amilton Antunes; Marques Júnior, Wilson
Source: Journal of the Peripheral Nervous System. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO PERIFÉRICO (GENÉTICA), AGENESIA, DIAGNÓSTICO DIFERENCIAL
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ABNT
LOURENÇO, Charles M. et al. Expanding the differencial diagnosis of inherited neuropathies with non-uniform conduction: andermann syndrome. Journal of the Peripheral Nervous System, v. 17, n. 1, p. 123-127, 2012Tradução . . Disponível em: https://doi.org/10.1111/j.1529-8027.2012.00374.x. Acesso em: 17 nov. 2024.
APA
Lourenço, C. M., Dupré, N., Rivière, J. -B., Rouleau, G. A., Marques, V. D., Genari, A. B., et al. (2012). Expanding the differencial diagnosis of inherited neuropathies with non-uniform conduction: andermann syndrome. Journal of the Peripheral Nervous System, 17( 1), 123-127. doi:10.1111/j.1529-8027.2012.00374.x
NLM
Lourenço CM, Dupré N, Rivière J-B, Rouleau GA, Marques VD, Genari AB, Santos AC dos, Barreira AA, Marques Júnior W. Expanding the differencial diagnosis of inherited neuropathies with non-uniform conduction: andermann syndrome [Internet]. Journal of the Peripheral Nervous System. 2012 ; 17( 1): 123-127.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1111/j.1529-8027.2012.00374.x
Vancouver
Lourenço CM, Dupré N, Rivière J-B, Rouleau GA, Marques VD, Genari AB, Santos AC dos, Barreira AA, Marques Júnior W. Expanding the differencial diagnosis of inherited neuropathies with non-uniform conduction: andermann syndrome [Internet]. Journal of the Peripheral Nervous System. 2012 ; 17( 1): 123-127.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1111/j.1529-8027.2012.00374.x
Artigo de periodico
HLA-DRB association in neuromyelitis optica is different from that observed in multiple sclerosis (2011)
Souza, Doralina Guimarães Brum; Barreira, Amilton Antunes; Santos, Antônio Carlos dos; Maciel, Damácio Ramón Kaimén; Matiello, Marcelo; Costa, Roberta Martins da Silva; Deghaide, Neifi Hassan Saloum; Costa, Laudo Silva; Louzada Junior, Paulo; Diniz, Paula Rejane Beserra; Frota, Elizabeth Regina Comini; Mendes Júnior, Celso Teixeira; Donadi, Eduardo Antônio
Source: Multiple Sclerosis. Unidades: FMRP, FFCLRP
Assunto: DOENÇAS DO SISTEMA NERVOSO
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ABNT
SOUZA, Doralina Guimarães Brum et al. HLA-DRB association in neuromyelitis optica is different from that observed in multiple sclerosis. Multiple Sclerosis, v. 16, n. 1, p. 21-29, 2011Tradução . . Disponível em: https://doi.org/10.1177/1352458509350741. Acesso em: 17 nov. 2024.
APA
Souza, D. G. B., Barreira, A. A., Santos, A. C. dos, Maciel, D. R. K., Matiello, M., Costa, R. M. da S., et al. (2011). HLA-DRB association in neuromyelitis optica is different from that observed in multiple sclerosis. Multiple Sclerosis, 16( 1), 21-29. doi:10.1177/1352458509350741
NLM
Souza DGB, Barreira AA, Santos AC dos, Maciel DRK, Matiello M, Costa RM da S, Deghaide NHS, Costa LS, Louzada Junior P, Diniz PRB, Frota ERC, Mendes Júnior CT, Donadi EA. HLA-DRB association in neuromyelitis optica is different from that observed in multiple sclerosis [Internet]. Multiple Sclerosis. 2011 ; 16( 1): 21-29.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1177/1352458509350741
Vancouver
Souza DGB, Barreira AA, Santos AC dos, Maciel DRK, Matiello M, Costa RM da S, Deghaide NHS, Costa LS, Louzada Junior P, Diniz PRB, Frota ERC, Mendes Júnior CT, Donadi EA. HLA-DRB association in neuromyelitis optica is different from that observed in multiple sclerosis [Internet]. Multiple Sclerosis. 2011 ; 16( 1): 21-29.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1177/1352458509350741
Artigo de periodico
Characterizing the phenotypic manifestations of MFN2 R104W mutation in charcot-marie-tooth type 2 (2011)
Genari, Adriana Borges; Borguetti, Vinícius Horácio Stefani; Gouvêa, Silmara Paula; Bueno, Keity Cristina; Santos, Patrícia Leila dos; Santos, Antônio Carlos dos; Barreira, Amilton Antunes; Lourenço, Charles Marques; Marques Júnior, Wilson
Source: Neuromuscular Disorders. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, FENÓTIPOS, DOENÇAS NEURODEGENERATIVAS
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ABNT
GENARI, Adriana Borges et al. Characterizing the phenotypic manifestations of MFN2 R104W mutation in charcot-marie-tooth type 2. Neuromuscular Disorders, v. 21, n. 6, p. 428-432, 2011Tradução . . Acesso em: 17 nov. 2024.
APA
Genari, A. B., Borguetti, V. H. S., Gouvêa, S. P., Bueno, K. C., Santos, P. L. dos, Santos, A. C. dos, et al. (2011). Characterizing the phenotypic manifestations of MFN2 R104W mutation in charcot-marie-tooth type 2. Neuromuscular Disorders, 21( 6), 428-432.
NLM
Genari AB, Borguetti VHS, Gouvêa SP, Bueno KC, Santos PL dos, Santos AC dos, Barreira AA, Lourenço CM, Marques Júnior W. Characterizing the phenotypic manifestations of MFN2 R104W mutation in charcot-marie-tooth type 2. Neuromuscular Disorders. 2011 ; 21( 6): 428-432.[citado 2024 nov. 17 ]
Vancouver
Genari AB, Borguetti VHS, Gouvêa SP, Bueno KC, Santos PL dos, Santos AC dos, Barreira AA, Lourenço CM, Marques Júnior W. Characterizing the phenotypic manifestations of MFN2 R104W mutation in charcot-marie-tooth type 2. Neuromuscular Disorders. 2011 ; 21( 6): 428-432.[citado 2024 nov. 17 ]
Artigo de periodico
Comparison of fingolimod with interferon beta-1a in relapsing-remitting multiple sclerosis: a randomised extension of the TRANSFORMS study (2011)
Khatri, Bhupendra; Barkhof, Frederik; Comi, Giancarlo; Hartung, Hans-Peter; Kappos, Ludwig; Montalban, Xavier; Pelletier, Jean; Stites, Tracy; Wu, Stacy; Holdbrook, Fred; Zhang-Auberson, Lixin; Francis, Gordon; Cohen, Jeffrey A.; Barreira, Amilton Antunes
Source: The Lancet Neurology. Unidade: FMRP
Subjects: ESCLEROSE MÚLTIPLA (TRATAMENTO), FÁRMACOS IMUNOSSUPRESSORES, ESTUDOS RANDOMIZADOS, PACIENTES (AVALIAÇÃO)
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ABNT
KHATRI, Bhupendra et al. Comparison of fingolimod with interferon beta-1a in relapsing-remitting multiple sclerosis: a randomised extension of the TRANSFORMS study. The Lancet Neurology, v. 10, n. 6, p. 520-529, 2011Tradução . . Disponível em: https://doi.org/10.1016/S1474-4422(11)70099-0. Acesso em: 17 nov. 2024.
APA
Khatri, B., Barkhof, F., Comi, G., Hartung, H. -P., Kappos, L., Montalban, X., et al. (2011). Comparison of fingolimod with interferon beta-1a in relapsing-remitting multiple sclerosis: a randomised extension of the TRANSFORMS study. The Lancet Neurology, 10( 6), 520-529. doi:10.1016/S1474-4422(11)70099-0
NLM
Khatri B, Barkhof F, Comi G, Hartung H-P, Kappos L, Montalban X, Pelletier J, Stites T, Wu S, Holdbrook F, Zhang-Auberson L, Francis G, Cohen JA, Barreira AA. Comparison of fingolimod with interferon beta-1a in relapsing-remitting multiple sclerosis: a randomised extension of the TRANSFORMS study [Internet]. The Lancet Neurology. 2011 ; 10( 6): 520-529.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/S1474-4422(11)70099-0
Vancouver
Khatri B, Barkhof F, Comi G, Hartung H-P, Kappos L, Montalban X, Pelletier J, Stites T, Wu S, Holdbrook F, Zhang-Auberson L, Francis G, Cohen JA, Barreira AA. Comparison of fingolimod with interferon beta-1a in relapsing-remitting multiple sclerosis: a randomised extension of the TRANSFORMS study [Internet]. The Lancet Neurology. 2011 ; 10( 6): 520-529.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/S1474-4422(11)70099-0
Artigo de periodico
Coexistence of two chronic neuropathies in a young child: Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyneuropathy (2010)
Marques Júnior, Wilson; Funayama, Carolina Araujo Rodrigues; Secchin, Juliana Bruneli; Lourenço, Charles Marques; Gouvêa, Silmara P.; Marques, Vanessa Daccach; Bastos, Patrícia Gomes; Barreira, Amilton Antunes
Source: Muscle & Nerve. Unidade: FMRP
Subjects: CRIANÇAS, DOENÇAS DO SISTEMA NERVOSO
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ABNT
MARQUES JÚNIOR, Wilson et al. Coexistence of two chronic neuropathies in a young child: Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyneuropathy. Muscle & Nerve, v. 42, n. 4, p. 598-600, 2010Tradução . . Disponível em: https://doi.org/10.1002/mus.21753. Acesso em: 17 nov. 2024.
APA
Marques Júnior, W., Funayama, C. A. R., Secchin, J. B., Lourenço, C. M., Gouvêa, S. P., Marques, V. D., et al. (2010). Coexistence of two chronic neuropathies in a young child: Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyneuropathy. Muscle & Nerve, 42( 4), 598-600. doi:10.1002/mus.21753
NLM
Marques Júnior W, Funayama CAR, Secchin JB, Lourenço CM, Gouvêa SP, Marques VD, Bastos PG, Barreira AA. Coexistence of two chronic neuropathies in a young child: Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyneuropathy [Internet]. Muscle & Nerve. 2010 ; 42( 4): 598-600.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/mus.21753
Vancouver
Marques Júnior W, Funayama CAR, Secchin JB, Lourenço CM, Gouvêa SP, Marques VD, Bastos PG, Barreira AA. Coexistence of two chronic neuropathies in a young child: Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyneuropathy [Internet]. Muscle & Nerve. 2010 ; 42( 4): 598-600.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/mus.21753
Artigo de periodico
Familial neuromyelitis optica (2010)
Matiello, M.; Kim, H. J.; Kim, W.; Brum, Doralina Guimarães; Barreira, Amilton Antunes; Kingsbury, D. J.; Plant, G. T.; Adoni, Tarso; Weinshenker, B. G.
Source: Neurology. Unidade: FMRP
Assunto: DOENÇAS DO SISTEMA NERVOSO
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ABNT
MATIELLO, M. et al. Familial neuromyelitis optica. Neurology, v. 75, n. 4, p. 310-315, 2010Tradução . . Disponível em: https://doi.org/10.1212/wnl.0b013e3181ea9f15. Acesso em: 17 nov. 2024.
APA
Matiello, M., Kim, H. J., Kim, W., Brum, D. G., Barreira, A. A., Kingsbury, D. J., et al. (2010). Familial neuromyelitis optica. Neurology, 75( 4), 310-315. doi:10.1212/wnl.0b013e3181ea9f15
NLM
Matiello M, Kim HJ, Kim W, Brum DG, Barreira AA, Kingsbury DJ, Plant GT, Adoni T, Weinshenker BG. Familial neuromyelitis optica [Internet]. Neurology. 2010 ; 75( 4): 310-315.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1212/wnl.0b013e3181ea9f15
Vancouver
Matiello M, Kim HJ, Kim W, Brum DG, Barreira AA, Kingsbury DJ, Plant GT, Adoni T, Weinshenker BG. Familial neuromyelitis optica [Internet]. Neurology. 2010 ; 75( 4): 310-315.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1212/wnl.0b013e3181ea9f15
Artigo de periodico
Brazilian experience with two conditioning regimers in patients with multiple sclerosis: BEAM/horse ATG and CY/rabbit ATG (2010)
Hamerschlak, Nelson; Rodrigues, Morgani; Moraes, Daniela Aparecida de; Rodrigues, Maria Carolina de Oliveira; Stracieri, Ana Beatriz Pereira Lima; Pieroni, Fabiano; Barros, George Maurício Navarro; Madeira, Maria Isabel Ayrosa; Simoes, Belinda Pinto; Barreira, Amilton Antunes; Brum, Doralina Guimarães; Ribeiro, Andreza Alice Feitosa; Kutner, José Mauro; Tylberi, C. P.; Porto, P. P.; Santana, C. L.; Neto, J. Z.; Barros, João Carlos; Paes, Angela Tavares; Burt, Richard K.; Oliveira-Cardoso, Érika Arantes de; Mastropietro, Ana Paula; Santos, Antônio Carlos dos; Voltarelli, Julio Cesar
Source: Bone Marrow Transplantation. Unidades: FMRP, FFCLRP
Subjects: DOENÇAS NEURODEGENERATIVAS, CÉLULAS-TRONCO
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ABNT
HAMERSCHLAK, Nelson et al. Brazilian experience with two conditioning regimers in patients with multiple sclerosis: BEAM/horse ATG and CY/rabbit ATG. Bone Marrow Transplantation, v. 45, n. 2, p. 239-248, 2010Tradução . . Disponível em: https://doi.org/10.1038/bmt.2009.127. Acesso em: 17 nov. 2024.
APA
Hamerschlak, N., Rodrigues, M., Moraes, D. A. de, Rodrigues, M. C. de O., Stracieri, A. B. P. L., Pieroni, F., et al. (2010). Brazilian experience with two conditioning regimers in patients with multiple sclerosis: BEAM/horse ATG and CY/rabbit ATG. Bone Marrow Transplantation, 45( 2), 239-248. doi:10.1038/bmt.2009.127
NLM
Hamerschlak N, Rodrigues M, Moraes DA de, Rodrigues MC de O, Stracieri ABPL, Pieroni F, Barros GMN, Madeira MIA, Simoes BP, Barreira AA, Brum DG, Ribeiro AAF, Kutner JM, Tylberi CP, Porto PP, Santana CL, Neto JZ, Barros JC, Paes AT, Burt RK, Oliveira-Cardoso ÉA de, Mastropietro AP, Santos AC dos, Voltarelli JC. Brazilian experience with two conditioning regimers in patients with multiple sclerosis: BEAM/horse ATG and CY/rabbit ATG [Internet]. Bone Marrow Transplantation. 2010 ; 45( 2): 239-248.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/bmt.2009.127
Vancouver
Hamerschlak N, Rodrigues M, Moraes DA de, Rodrigues MC de O, Stracieri ABPL, Pieroni F, Barros GMN, Madeira MIA, Simoes BP, Barreira AA, Brum DG, Ribeiro AAF, Kutner JM, Tylberi CP, Porto PP, Santana CL, Neto JZ, Barros JC, Paes AT, Burt RK, Oliveira-Cardoso ÉA de, Mastropietro AP, Santos AC dos, Voltarelli JC. Brazilian experience with two conditioning regimers in patients with multiple sclerosis: BEAM/horse ATG and CY/rabbit ATG [Internet]. Bone Marrow Transplantation. 2010 ; 45( 2): 239-248.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/bmt.2009.127
Artigo de periodico
Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis (2010)
Cohen, Jeffrey A.; Barkhof, Frederik; Comi, Giancarlo; Hartung, Hans-Peter; Khatri, Bhupendra O.; Montalban, Xavier; Pelletier, Jean; Capra, Ruggero; Gallo, Paolo; Izquierdo, Guillermo; Tiel-Wilck, Klaus; Vera, Ana de; Jin, James; Stites, Tracy; Wu, Stacy; Aradhye, Shreeram; Kappos, Ludwig; Barreira, Amilton Antunes
Source: New England Journal of Medicine. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, FÁRMACOS IMUNOSSUPRESSORES
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ABNT
COHEN, Jeffrey A. et al. Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. New England Journal of Medicine, v. 362, n. 5, p. 402-415, 2010Tradução . . Acesso em: 17 nov. 2024.
APA
Cohen, J. A., Barkhof, F., Comi, G., Hartung, H. -P., Khatri, B. O., Montalban, X., et al. (2010). Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. New England Journal of Medicine, 362( 5), 402-415.
NLM
Cohen JA, Barkhof F, Comi G, Hartung H-P, Khatri BO, Montalban X, Pelletier J, Capra R, Gallo P, Izquierdo G, Tiel-Wilck K, Vera A de, Jin J, Stites T, Wu S, Aradhye S, Kappos L, Barreira AA. Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. New England Journal of Medicine. 2010 ; 362( 5): 402-415.[citado 2024 nov. 17 ]
Vancouver
Cohen JA, Barkhof F, Comi G, Hartung H-P, Khatri BO, Montalban X, Pelletier J, Capra R, Gallo P, Izquierdo G, Tiel-Wilck K, Vera A de, Jin J, Stites T, Wu S, Aradhye S, Kappos L, Barreira AA. Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. New England Journal of Medicine. 2010 ; 362( 5): 402-415.[citado 2024 nov. 17 ]
Artigo de periodico
Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course (2009)
Sobreira, Cláudia Ferreira da Rosa; Marques Júnior, Wilson; Pontes-Neto, Octávio Marques; Santos, Antônio Carlos dos; Pina Neto, João Monteiro de; Barreira, Amilton Antunes
Source: Journal of the Neurological Sciences. Unidade: FMRP
Subjects: NEUROLOGIA, MUTAÇÃO GENÉTICA, MITOCÔNDRIAS
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ABNT
SOBREIRA, Cláudia Ferreira da Rosa et al. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course. Journal of the Neurological Sciences, v. 278, n. 1-2, p. 132-134, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.jns.2008.11.023. Acesso em: 17 nov. 2024.
APA
Sobreira, C. F. da R., Marques Júnior, W., Pontes-Neto, O. M., Santos, A. C. dos, Pina Neto, J. M. de, & Barreira, A. A. (2009). Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course. Journal of the Neurological Sciences, 278( 1-2), 132-134. doi:10.1016/j.jns.2008.11.023
NLM
Sobreira CF da R, Marques Júnior W, Pontes-Neto OM, Santos AC dos, Pina Neto JM de, Barreira AA. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course [Internet]. Journal of the Neurological Sciences. 2009 ; 278( 1-2): 132-134.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.jns.2008.11.023
Vancouver
Sobreira CF da R, Marques Júnior W, Pontes-Neto OM, Santos AC dos, Pina Neto JM de, Barreira AA. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course [Internet]. Journal of the Neurological Sciences. 2009 ; 278( 1-2): 132-134.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.jns.2008.11.023

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