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Artigo de periodico
Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype (2022)
Shelton, G. Diane ; Minor, Katie M; Vieira, Natassia M; Kunkel, Louis M; Friedenberg, Steven G; Cullen, Jonah N; Guo, Ling T; Zatz, Mayana ; Mickelson, James R
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, SEQUENCIAMENTO GENÉTICO, MIOPATIAS CONGÊNITAS ESTRUTURAIS, CÃO GOLDEN RETRIEVER
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ABNT
SHELTON, G. Diane et al. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders, v. 32, n. 10, p. 836-841, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2022.08.001. Acesso em: 08 out. 2024.
APA
Shelton, G. D., Minor, K. M., Vieira, N. M., Kunkel, L. M., Friedenberg, S. G., Cullen, J. N., et al. (2022). Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders, 32( 10), 836-841. doi:10.1016/j.nmd.2022.08.001
NLM
Shelton GD, Minor KM, Vieira NM, Kunkel LM, Friedenberg SG, Cullen JN, Guo LT, Zatz M, Mickelson JR. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype [Internet]. Neuromuscular Disorders. 2022 ; 32( 10): 836-841.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2022.08.001
Vancouver
Shelton GD, Minor KM, Vieira NM, Kunkel LM, Friedenberg SG, Cullen JN, Guo LT, Zatz M, Mickelson JR. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype [Internet]. Neuromuscular Disorders. 2022 ; 32( 10): 836-841.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2022.08.001
Artigo de periodico
Sarcoglycanopathies: an update (2021)
Vainzof, Mariz ; Souza, Lucas S; Gurgel-Giannetti, Juliana; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, EXPRESSÃO GÊNICA, MUTAÇÃO GENÉTICA, GENES
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ABNT
VAINZOF, Mariz et al. Sarcoglycanopathies: an update. Neuromuscular Disorders, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2021.07.014. Acesso em: 08 out. 2024.
APA
Vainzof, M., Souza, L. S., Gurgel-Giannetti, J., & Zatz, M. (2021). Sarcoglycanopathies: an update. Neuromuscular Disorders. doi:10.1016/j.nmd.2021.07.014
NLM
Vainzof M, Souza LS, Gurgel-Giannetti J, Zatz M. Sarcoglycanopathies: an update [Internet]. Neuromuscular Disorders. 2021 ;[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2021.07.014
Vancouver
Vainzof M, Souza LS, Gurgel-Giannetti J, Zatz M. Sarcoglycanopathies: an update [Internet]. Neuromuscular Disorders. 2021 ;[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2021.07.014
Artigo de periodico
Risk factors and future directions for preventing and diagnosing exertional rhabdomyolysis (2021)
Carneiro, Andréia; Gomes, Diego Viana ; Silva, Janaina Macedo da ; Lima, Giscard Humberto Oliveira ; Nogueira, Simone Mitri ; Alves, Sergio Rabello ; Turner, Alexander Kolliari ; Zanoteli, Edmar ; Aquino Neto, Francisco Radler de ; Palmisano, Giuseppe ; Pesquero, João Bosco ; Moreira, Josino Costa ; Pereira, Marcos Dias
Source: Neuromuscular Disorders. Unidades: FM, ICB
Subjects: PARASITOLOGIA, INSUFICIÊNCIA RENAL AGUDA, EPIGÊNESE GENÉTICA, POLIMORFISMO, PROTEÔMICA, FATORES DE RISCO, EXERCÍCIO FÍSICO, MÚSCULO ESQUELÉTICO, PROTEÍNAS SANGUÍNEAS
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ABNT
CARNEIRO, Andréia et al. Risk factors and future directions for preventing and diagnosing exertional rhabdomyolysis. Neuromuscular Disorders, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2021.04.007. Acesso em: 08 out. 2024.
APA
Carneiro, A., Gomes, D. V., Silva, J. M. da, Lima, G. H. O., Nogueira, S. M., Alves, S. R., et al. (2021). Risk factors and future directions for preventing and diagnosing exertional rhabdomyolysis. Neuromuscular Disorders. doi:10.1016/j.nmd.2021.04.007
NLM
Carneiro A, Gomes DV, Silva JM da, Lima GHO, Nogueira SM, Alves SR, Turner AK, Zanoteli E, Aquino Neto FR de, Palmisano G, Pesquero JB, Moreira JC, Pereira MD. Risk factors and future directions for preventing and diagnosing exertional rhabdomyolysis [Internet]. Neuromuscular Disorders. 2021 ;[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2021.04.007
Vancouver
Carneiro A, Gomes DV, Silva JM da, Lima GHO, Nogueira SM, Alves SR, Turner AK, Zanoteli E, Aquino Neto FR de, Palmisano G, Pesquero JB, Moreira JC, Pereira MD. Risk factors and future directions for preventing and diagnosing exertional rhabdomyolysis [Internet]. Neuromuscular Disorders. 2021 ;[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2021.04.007
Artigo de periodico
GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease (2021)
Figueiredo, Fernanda Barbosa ; Silva Junior, Wilson Araújo da ; Giuliatti, Silvana ; Tomaselli, Pedro José; Lourenço, Charles Marques; Gouvêa, Silmara Paula; Covaleski, Anna Paula Paranhos Miranda; Hallak, Jaime Eduardo Cecilio ; Marques Júnior, Wilson
Source: Neuromuscular Disorders. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, DOENÇAS DEGENERATIVAS, MUTAÇÃO GENÉTICA
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ABNT
FIGUEIREDO, Fernanda Barbosa et al. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, v. 31, n. 6, p. 505-511, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2021.03.005. Acesso em: 08 out. 2024.
APA
Figueiredo, F. B., Silva Junior, W. A. da, Giuliatti, S., Tomaselli, P. J., Lourenço, C. M., Gouvêa, S. P., et al. (2021). GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, 31( 6), 505-511. doi:10.1016/j.nmd.2021.03.005
NLM
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005
Vancouver
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005
Artigo de periodico
233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 (2018)
Lostal, William ; Urtizberea, J. Andoni; Richard, Isabelle ; Alonso-Jiménez, Alicia ; Carlier, Robert-Yves; Carson, Vincent ; Diaz-Manera, Jordi ; Eymard, Bruno; Fardeau, Michel; Gourlay, Marie-Laurence; Guglieri, Michela ; Hogrel, Jean-Yves ; Kullmann, Bruno; Levy, Jennifer ; Ono, Yasuko ; Prigent, Hélène ; Saenz, Amets ; Semplicini, Claudio ; Vainzof, Mariz ; Vissing, John ; Maggie, Walter
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, ENZIMAS, AMINOÁCIDOS, ENSAIO CLÍNICO
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ABNT
LOSTAL, William et al. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017. Neuromuscular Disorders, v. 28, p. 540-549, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2018.03.010. Acesso em: 08 out. 2024.
APA
Lostal, W., Urtizberea, J. A., Richard, I., Alonso-Jiménez, A., Carlier, R. -Y., Carson, V., et al. (2018). 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017. Neuromuscular Disorders, 28, 540-549. doi:10.1016/j.nmd.2018.03.010
NLM
Lostal W, Urtizberea JA, Richard I, Alonso-Jiménez A, Carlier R-Y, Carson V, Diaz-Manera J, Eymard B, Fardeau M, Gourlay M-L, Guglieri M, Hogrel J-Y, Kullmann B, Levy J, Ono Y, Prigent H, Saenz A, Semplicini C, Vainzof M, Vissing J, Maggie W. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 [Internet]. Neuromuscular Disorders. 2018 ; 28 540-549.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2018.03.010
Vancouver
Lostal W, Urtizberea JA, Richard I, Alonso-Jiménez A, Carlier R-Y, Carson V, Diaz-Manera J, Eymard B, Fardeau M, Gourlay M-L, Guglieri M, Hogrel J-Y, Kullmann B, Levy J, Ono Y, Prigent H, Saenz A, Semplicini C, Vainzof M, Vissing J, Maggie W. 233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 [Internet]. Neuromuscular Disorders. 2018 ; 28 540-549.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2018.03.010
Trabalho de evento-resumo periodico
High frequency of manifesting carriers in the recessive X-linked myotubular myopathy (2018)
Souza, L; Almeida, C; Silva, L; Pavanello, R; Gurgel-Gianneti, J; Zanoteli, E; Zatz, Mayana ; Otto, Paulo A ; Vainzof, Mariz
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society - WMS. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DOENÇAS RARAS, MUTAÇÃO GENÉTICA, DOENÇAS NEUROMUSCULARES, MIOPATIAS CONGÊNITAS ESTRUTURAIS, CROMOSSOMO X
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ABNT
SOUZA, L et al. High frequency of manifesting carriers in the recessive X-linked myotubular myopathy. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2018.06.169. Acesso em: 08 out. 2024. , 2018
APA
Souza, L., Almeida, C., Silva, L., Pavanello, R., Gurgel-Gianneti, J., Zanoteli, E., et al. (2018). High frequency of manifesting carriers in the recessive X-linked myotubular myopathy. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2018.06.169
NLM
Souza L, Almeida C, Silva L, Pavanello R, Gurgel-Gianneti J, Zanoteli E, Zatz M, Otto PA, Vainzof M. High frequency of manifesting carriers in the recessive X-linked myotubular myopathy [Internet]. Neuromuscular Disorders. 2018 ; 28 S72.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2018.06.169
Vancouver
Souza L, Almeida C, Silva L, Pavanello R, Gurgel-Gianneti J, Zanoteli E, Zatz M, Otto PA, Vainzof M. High frequency of manifesting carriers in the recessive X-linked myotubular myopathy [Internet]. Neuromuscular Disorders. 2018 ; 28 S72.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2018.06.169
Trabalho de evento-resumo periodico
Osteopontin expression during chronic and acute muscle injury (2017)
Tasaki, L; Ishiba, R; Ayub-Guerrieri, D; Almeida, C; Fernandes, S; Ribeiro Jr., A; Galleni, L; Souza, L; Santos, A; Vainzof, Mariz
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, DISTROFIA MUSCULAR, EXPRESSÃO GÊNICA, MODELOS ANIMAIS, PROTEÍNAS MUSCULARES, BIOLOGIA CELULAR, GENÉTICA MÉDICA
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ABNT
TASAKI, L et al. Osteopontin expression during chronic and acute muscle injury. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2017.06.360. Acesso em: 08 out. 2024. , 2017
APA
Tasaki, L., Ishiba, R., Ayub-Guerrieri, D., Almeida, C., Fernandes, S., Ribeiro Jr., A., et al. (2017). Osteopontin expression during chronic and acute muscle injury. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2017.06.360
NLM
Tasaki L, Ishiba R, Ayub-Guerrieri D, Almeida C, Fernandes S, Ribeiro Jr. A, Galleni L, Souza L, Santos A, Vainzof M. Osteopontin expression during chronic and acute muscle injury [Internet]. Neuromuscular Disorders. 2017 ; 27 S193.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2017.06.360
Vancouver
Tasaki L, Ishiba R, Ayub-Guerrieri D, Almeida C, Fernandes S, Ribeiro Jr. A, Galleni L, Souza L, Santos A, Vainzof M. Osteopontin expression during chronic and acute muscle injury [Internet]. Neuromuscular Disorders. 2017 ; 27 S193.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2017.06.360
Artigo de periodico
Matching pairs difficulty in children with spinal muscular atrophy type I (2017)
Polido, Graziela Jorge; Barbosa, Alessandra Ferreira; Morimoto, Carlos Hitoshi ; Caromano, Fátima Aparecida; Favero, Francis Meire; Zanoteli, Edmar; Reed, Umbertina Conti; Voos, Mariana Callil
Source: Neuromuscular Disorders. Unidades: FM, IME
Subjects: CRIANÇAS, PERCEPÇÃO VISUAL, ATROFIS MUSCULAR, COGNIÇÃO
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ABNT
POLIDO, Graziela Jorge et al. Matching pairs difficulty in children with spinal muscular atrophy type I. Neuromuscular Disorders, v. 27, n. 5, p. 419-427, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2017.01.017. Acesso em: 08 out. 2024.
APA
Polido, G. J., Barbosa, A. F., Morimoto, C. H., Caromano, F. A., Favero, F. M., Zanoteli, E., et al. (2017). Matching pairs difficulty in children with spinal muscular atrophy type I. Neuromuscular Disorders, 27( 5), 419-427. doi:10.1016/j.nmd.2017.01.017
NLM
Polido GJ, Barbosa AF, Morimoto CH, Caromano FA, Favero FM, Zanoteli E, Reed UC, Voos MC. Matching pairs difficulty in children with spinal muscular atrophy type I [Internet]. Neuromuscular Disorders. 2017 ; 27( 5): 419-427.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2017.01.017
Vancouver
Polido GJ, Barbosa AF, Morimoto CH, Caromano FA, Favero FM, Zanoteli E, Reed UC, Voos MC. Matching pairs difficulty in children with spinal muscular atrophy type I [Internet]. Neuromuscular Disorders. 2017 ; 27( 5): 419-427.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2017.01.017
Trabalho de evento-resumo periodico
Jagged1 as a modifier of the DMD phenotype: what is next? (2016)
Vieira, N; Assoni, Amanda Faria; Elvers, Ingegerd; Alexander, Matthew S; Eran, Alal; Marshall, J; Verjovski-Almeida, Sergio ; Lindblad-Toh, Kerstin; Kunkel, Louis M; Zatz, Mayana
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidades: IQ, IB
Subjects: FENÓTIPOS, DOENÇAS NEUROMUSCULARES
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ABNT
VIEIRA, N et al. Jagged1 as a modifier of the DMD phenotype: what is next?. Neuromuscular Disorders. Oxford: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2016.06.255. Acesso em: 08 out. 2024. , 2016
APA
Vieira, N., Assoni, A. F., Elvers, I., Alexander, M. S., Eran, A., Marshall, J., et al. (2016). Jagged1 as a modifier of the DMD phenotype: what is next? Neuromuscular Disorders. Oxford: Instituto de Química, Universidade de São Paulo. doi:10.1016/j.nmd.2016.06.255
NLM
Vieira N, Assoni AF, Elvers I, Alexander MS, Eran A, Marshall J, Verjovski-Almeida S, Lindblad-Toh K, Kunkel LM, Zatz M. Jagged1 as a modifier of the DMD phenotype: what is next? [Internet]. Neuromuscular Disorders. 2016 ; 26 S156 res. P.225.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2016.06.255
Vancouver
Vieira N, Assoni AF, Elvers I, Alexander MS, Eran A, Marshall J, Verjovski-Almeida S, Lindblad-Toh K, Kunkel LM, Zatz M. Jagged1 as a modifier of the DMD phenotype: what is next? [Internet]. Neuromuscular Disorders. 2016 ; 26 S156 res. P.225.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2016.06.255
Trabalho de evento-resumo periodico
Controversial preclinical results in neuromuscular animal models: are they related to differences in mesenchymal stromal cells (MSCs) secretome? (2016)
Assoni, A; Coatti, G.; Beccari, M.; Gomes, J; Cardozo, K; Neto, M; Carvalho, V; Zatz, Mayana
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DOENÇAS NEUROMUSCULARES, MODELOS ANIMAIS DE DOENÇAS, CÉLULAS ESTROMAIS
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ABNT
ASSONI, A et al. Controversial preclinical results in neuromuscular animal models: are they related to differences in mesenchymal stromal cells (MSCs) secretome?. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2016.06.156. Acesso em: 08 out. 2024. , 2016
APA
Assoni, A., Coatti, G., Beccari, M., Gomes, J., Cardozo, K., Neto, M., et al. (2016). Controversial preclinical results in neuromuscular animal models: are they related to differences in mesenchymal stromal cells (MSCs) secretome? Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2016.06.156
NLM
Assoni A, Coatti G, Beccari M, Gomes J, Cardozo K, Neto M, Carvalho V, Zatz M. Controversial preclinical results in neuromuscular animal models: are they related to differences in mesenchymal stromal cells (MSCs) secretome? [Internet]. Neuromuscular Disorders. 2016 ; 26 S128.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2016.06.156
Vancouver
Assoni A, Coatti G, Beccari M, Gomes J, Cardozo K, Neto M, Carvalho V, Zatz M. Controversial preclinical results in neuromuscular animal models: are they related to differences in mesenchymal stromal cells (MSCs) secretome? [Internet]. Neuromuscular Disorders. 2016 ; 26 S128.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2016.06.156
Artigo de periodico
Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers (2016)
Vainzof, Mariz ; Feitosa, Leticia; Canovas, Marta; Ayub-Guerrieri, Danielle; Pavanello, Rita de Cássia M; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, PROTEÍNAS MUSCULARES, MUTAÇÃO GENÉTICA, ESTUDO DE CASO, GENÉTICA MÉDICA
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ABNT
VAINZOF, Mariz et al. Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers. Neuromuscular Disorders, v. 26, n. 3, p. 197-200, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2016.01.001. Acesso em: 08 out. 2024.
APA
Vainzof, M., Feitosa, L., Canovas, M., Ayub-Guerrieri, D., Pavanello, R. de C. M., & Zatz, M. (2016). Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers. Neuromuscular Disorders, 26( 3), 197-200. doi:10.1016/j.nmd.2016.01.001
NLM
Vainzof M, Feitosa L, Canovas M, Ayub-Guerrieri D, Pavanello R de CM, Zatz M. Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers [Internet]. Neuromuscular Disorders. 2016 ; 26( 3): 197-200.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2016.01.001
Vancouver
Vainzof M, Feitosa L, Canovas M, Ayub-Guerrieri D, Pavanello R de CM, Zatz M. Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers [Internet]. Neuromuscular Disorders. 2016 ; 26( 3): 197-200.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2016.01.001
Trabalho de evento-resumo periodico
Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies (2016)
Ayub-Guerrieri, D; Ribeiro Junior, A; Ishiba, R; Yumi, L; Semedo-Kuriki, P; Vainzof, Mariz
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, DOENÇAS DEGENERATIVAS, MODELOS ANIMAIS DE DOENÇAS, CÉLULAS-TRONCO
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ABNT
AYUB-GUERRIERI, D et al. Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2016.06.155. Acesso em: 08 out. 2024. , 2016
APA
Ayub-Guerrieri, D., Ribeiro Junior, A., Ishiba, R., Yumi, L., Semedo-Kuriki, P., & Vainzof, M. (2016). Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2016.06.155
NLM
Ayub-Guerrieri D, Ribeiro Junior A, Ishiba R, Yumi L, Semedo-Kuriki P, Vainzof M. Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies [Internet]. Neuromuscular Disorders. 2016 ; 26 S128.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2016.06.155
Vancouver
Ayub-Guerrieri D, Ribeiro Junior A, Ishiba R, Yumi L, Semedo-Kuriki P, Vainzof M. Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies [Internet]. Neuromuscular Disorders. 2016 ; 26 S128.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2016.06.155
Trabalho de evento-resumo periodico
The relevance of timed movements on functional assessment in Duchenne muscular dystrophy (2015)
Voos, M.; Martini, J.; Simões, M.; Hukuda, M.; Favero, F.; Oliveira, A.; Caromano, F.
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Subjects: DISTROFIA MUSCULAR, CRIANÇAS, DOENÇAS MUSCULOSQUELÉTICAS
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ABNT
VOOS, M. et al. The relevance of timed movements on functional assessment in Duchenne muscular dystrophy. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2015.06.165. Acesso em: 08 out. 2024. , 2015
APA
Voos, M., Martini, J., Simões, M., Hukuda, M., Favero, F., Oliveira, A., & Caromano, F. (2015). The relevance of timed movements on functional assessment in Duchenne muscular dystrophy. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2015.06.165
NLM
Voos M, Martini J, Simões M, Hukuda M, Favero F, Oliveira A, Caromano F. The relevance of timed movements on functional assessment in Duchenne muscular dystrophy [Internet]. Neuromuscular Disorders. 2015 ; 25 S230.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.165
Vancouver
Voos M, Martini J, Simões M, Hukuda M, Favero F, Oliveira A, Caromano F. The relevance of timed movements on functional assessment in Duchenne muscular dystrophy [Internet]. Neuromuscular Disorders. 2015 ; 25 S230.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.165
Trabalho de evento-resumo periodico
RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges (2015)
Gardiner, A.; Scalco, R.; Parton, M.; Hanna, M.; Pitceathly, R.; Zanoteli, E.; Murphy, E.; Treves, S.; Houlden, H.; Wilmshurst, J.; Straub, V.; Hilton-Jones, D.; Voermans, N.; Manzur, A.; Oflazer, P.; Reed, U.; Lachmann, R.; Quinlivan, R.; Jungbluth, H.
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Subjects: DOENÇAS MUSCULARES, PROTEÍNAS MUSCULARES, DOENÇAS MUSCULOSQUELÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARDINER, A. et al. RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2015.06.263. Acesso em: 08 out. 2024. , 2015
APA
Gardiner, A., Scalco, R., Parton, M., Hanna, M., Pitceathly, R., Zanoteli, E., et al. (2015). RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2015.06.263
NLM
Gardiner A, Scalco R, Parton M, Hanna M, Pitceathly R, Zanoteli E, Murphy E, Treves S, Houlden H, Wilmshurst J, Straub V, Hilton-Jones D, Voermans N, Manzur A, Oflazer P, Reed U, Lachmann R, Quinlivan R, Jungbluth H. RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges [Internet]. Neuromuscular Disorders. 2015 ; 25 S257-S258.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.263
Vancouver
Gardiner A, Scalco R, Parton M, Hanna M, Pitceathly R, Zanoteli E, Murphy E, Treves S, Houlden H, Wilmshurst J, Straub V, Hilton-Jones D, Voermans N, Manzur A, Oflazer P, Reed U, Lachmann R, Quinlivan R, Jungbluth H. RYR1-related exertional rhabdomyolysis: Expanding spectrum and diagnostic challenges [Internet]. Neuromuscular Disorders. 2015 ; 25 S257-S258.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.263
Artigo de periodico-carta/editorial
Response to: milder course in Duchenne patients with nonsense mutations and no muscle dystrophin. [Carta] (2015)
Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, PROTEÍNAS MUSCULARES, HORMÔNIO DO CRESCIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana. Response to: milder course in Duchenne patients with nonsense mutations and no muscle dystrophin. [Carta]. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2015.02.010. Acesso em: 08 out. 2024. , 2015
APA
Zatz, M. (2015). Response to: milder course in Duchenne patients with nonsense mutations and no muscle dystrophin. [Carta]. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2015.02.010
NLM
Zatz M. Response to: milder course in Duchenne patients with nonsense mutations and no muscle dystrophin. [Carta] [Internet]. Neuromuscular Disorders. 2015 ; 25 444.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.010
Vancouver
Zatz M. Response to: milder course in Duchenne patients with nonsense mutations and no muscle dystrophin. [Carta] [Internet]. Neuromuscular Disorders. 2015 ; 25 444.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.010
Artigo de periodico
A normal life without muscle dystrophin (2015)
Zatz, Mayana ; Vieira, N. M.; Zucconi, E.; Pelatti, M.; Vainzof, Mariz ; Martins-Bach, A. B.; Otaduy, M. C. Garcia; Santos, G. Bento dos; Amaro Jr., E.; Landini, V.; Andrade, T.
Source: Neuromuscular Disorders. Unidades: IB, FM
Subjects: DOENÇAS MUSCULARES EM ANIMAL, CÃES DE CAÇA, DISTROFIA MUSCULAR ANIMAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. A normal life without muscle dystrophin. Neuromuscular Disorders, v. 25, n. 5, p. 371-374, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2015.02.007. Acesso em: 08 out. 2024.
APA
Zatz, M., Vieira, N. M., Zucconi, E., Pelatti, M., Vainzof, M., Martins-Bach, A. B., et al. (2015). A normal life without muscle dystrophin. Neuromuscular Disorders, 25( 5), 371-374. doi:10.1016/j.nmd.2015.02.007
NLM
Zatz M, Vieira NM, Zucconi E, Pelatti M, Vainzof M, Martins-Bach AB, Otaduy MCG, Santos GB dos, Amaro Jr. E, Landini V, Andrade T. A normal life without muscle dystrophin [Internet]. Neuromuscular Disorders. 2015 ; 25( 5): 371-374.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.007
Vancouver
Zatz M, Vieira NM, Zucconi E, Pelatti M, Vainzof M, Martins-Bach AB, Otaduy MCG, Santos GB dos, Amaro Jr. E, Landini V, Andrade T. A normal life without muscle dystrophin [Internet]. Neuromuscular Disorders. 2015 ; 25( 5): 371-374.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.007
Trabalho de evento-resumo periodico
Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita (2015)
Ravenscroft, G.; Nolent, F.; Rajagopalan, S.; Meireles, A.; Paavola, K.; Gaillard, D.; Alanio, E.; Buckland, M.; Arbuckle, S.; Krivanek, M.; Maluenda, J.; Pannell, S.; Gooding, R.; Ong, R.; Allcock, R.; Kok, F.; Talbot, W.; Melki, J.; Laing, N.
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Subjects: MOVIMENTO FETAL, MALFORMAÇÕES, ANORMALIDADES MUSCULOSQUELÉTICAS, ARTROPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAVENSCROFT, G. et al. Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2015.06.013. Acesso em: 08 out. 2024. , 2015
APA
Ravenscroft, G., Nolent, F., Rajagopalan, S., Meireles, A., Paavola, K., Gaillard, D., et al. (2015). Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2015.06.013
NLM
Ravenscroft G, Nolent F, Rajagopalan S, Meireles A, Paavola K, Gaillard D, Alanio E, Buckland M, Arbuckle S, Krivanek M, Maluenda J, Pannell S, Gooding R, Ong R, Allcock R, Kok F, Talbot W, Melki J, Laing N. Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita [Internet]. Neuromuscular Disorders. 2015 ; 25 S186.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.013
Vancouver
Ravenscroft G, Nolent F, Rajagopalan S, Meireles A, Paavola K, Gaillard D, Alanio E, Buckland M, Arbuckle S, Krivanek M, Maluenda J, Pannell S, Gooding R, Ong R, Allcock R, Kok F, Talbot W, Melki J, Laing N. Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita [Internet]. Neuromuscular Disorders. 2015 ; 25 S186.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.013
Trabalho de evento-resumo periodico
Responsiveness of the Functional Evaluation Scale for patients with Duchenne muscular dystrophy – domain 1: Sitting and rising from the chair (2015)
Voos, M.; Hukuda, M.; Carvalho, E. de; Caromano, F.
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Subjects: DISTROFIA MUSCULAR, CRIANÇAS, ESTUDOS LONGITUDINAIS, ESTUDOS RETROSPECTIVOS, DOENÇAS MUSCULOSQUELÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VOOS, M. et al. Responsiveness of the Functional Evaluation Scale for patients with Duchenne muscular dystrophy – domain 1: Sitting and rising from the chair. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2015.06.166. Acesso em: 08 out. 2024. , 2015
APA
Voos, M., Hukuda, M., Carvalho, E. de, & Caromano, F. (2015). Responsiveness of the Functional Evaluation Scale for patients with Duchenne muscular dystrophy – domain 1: Sitting and rising from the chair. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2015.06.166
NLM
Voos M, Hukuda M, Carvalho E de, Caromano F. Responsiveness of the Functional Evaluation Scale for patients with Duchenne muscular dystrophy – domain 1: Sitting and rising from the chair [Internet]. Neuromuscular Disorders. 2015 ; 25 S230.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.166
Vancouver
Voos M, Hukuda M, Carvalho E de, Caromano F. Responsiveness of the Functional Evaluation Scale for patients with Duchenne muscular dystrophy – domain 1: Sitting and rising from the chair [Internet]. Neuromuscular Disorders. 2015 ; 25 S230.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.166
Trabalho de evento-resumo periodico
Stabilometric findings in children and adolescent with Charcot-Marie-Tooth disease (2015)
Mattiello Sverzut, Ana Cláudia; Baptista, C.; Calori, P.; Garcia, B.; Marques Júnior, Wilson
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FMRP
Subjects: DOENÇAS NEUROMUSCULARES, CRIANÇAS, EQUILÍBRIO MUSCULOSQUELÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MATTIELLO SVERZUT, Ana Cláudia et al. Stabilometric findings in children and adolescent with Charcot-Marie-Tooth disease. Neuromuscular Disorders. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2015.06.352. Acesso em: 08 out. 2024. , 2015
APA
Mattiello Sverzut, A. C., Baptista, C., Calori, P., Garcia, B., & Marques Júnior, W. (2015). Stabilometric findings in children and adolescent with Charcot-Marie-Tooth disease. Neuromuscular Disorders. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1016/j.nmd.2015.06.352
NLM
Mattiello Sverzut AC, Baptista C, Calori P, Garcia B, Marques Júnior W. Stabilometric findings in children and adolescent with Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2015 ; 25 S284.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.352
Vancouver
Mattiello Sverzut AC, Baptista C, Calori P, Garcia B, Marques Júnior W. Stabilometric findings in children and adolescent with Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2015 ; 25 S284.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.352
Artigo de periodico
Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype (2015)
Vieira, Natássia M; Guo, Ling T; Estrela, Elicia; Kunkel, Louis M; Zatz, Mayana ; Shelton, G. Diane
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MODELOS ANIMAIS, CÃO LABRADOR RETRIEVER, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIEIRA, Natássia M et al. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype. Neuromuscular Disorders, v. 25, p. 363-370, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2015.02.012. Acesso em: 08 out. 2024.
APA
Vieira, N. M., Guo, L. T., Estrela, E., Kunkel, L. M., Zatz, M., & Shelton, G. D. (2015). Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype. Neuromuscular Disorders, 25, 363-370. doi:10.1016/j.nmd.2015.02.012
NLM
Vieira NM, Guo LT, Estrela E, Kunkel LM, Zatz M, Shelton GD. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype [Internet]. Neuromuscular Disorders. 2015 ; 25 363-370.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.012
Vancouver
Vieira NM, Guo LT, Estrela E, Kunkel LM, Zatz M, Shelton GD. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype [Internet]. Neuromuscular Disorders. 2015 ; 25 363-370.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.012

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