Human Adipose-Derived Mesenchymal Stromal Cells Injected Systemically into GRMD Dogs without Immunosuppression are Able to Reach the Host Muscle and Express Human Dystrophin
Vieira, N. M., Valadares, M., Zucconi, E., Secco, M., Junior, C. R. Bueno, Brandalise, V., Assoni, A., Gomes, J., Landini, V., Andrade, T., Caetano, H. V. A., Vainzof, M., Zatz, M.
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Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin
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Mild course in atypical Duchenne muscular dystrophy patients is not caused by utrophin overexpression
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Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies
Ayub-Guerrieri, D, Ribeiro, A, Ishiba, R, Yumi, L, Semedo-Kuriki, P, Vainzof, M
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G.P.19
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Nemaline myopathy: Clinical, pathological, muscle imaging and molecular characterization in a cohort of Brazilian patients
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Published in Neuromuscular disorders : NMD (01.10.2016)
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A normal life without muscle dystrophin
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Published in Neuromuscular disorders : NMD (01.10.2014)
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Long term follow-up of GRMD dogs transplanted with human adipose derived stem cells
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Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Nemaline myopathy: Next generation sequencing (NGS) significantly improving the molecular classification of Brazilian families
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Published in Neuromuscular disorders : NMD (01.10.2015)
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Next generation sequencing (NGS): A powerful tool for studying rigid spine patients and multiminicore myopathy
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Published in Neuromuscular disorders : NMD (01.10.2015)
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Steroid benefit in a laminopathy-congenital muscular dystrophy patient with dropped head syndrome: A 10-year follow-up
Gurgel-Giannetti, J, Ribeiro, B, Uliana, L, Sampaio, G, Giannetti, A, Van der Linden, V, Vainzof, M
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Published in Neuromuscular disorders : NMD (01.10.2015)
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P.5.8 Why is LGMD2G rare?
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Published in Neuromuscular disorders : NMD (01.10.2013)
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A.P.14
Vainzof, M, Lazar, M, Yamamoto, G.L, Almeida, C.F, Onofre-Oliveira, P, Nogueira, L, Yamamoto, L.U, Zatz, M, Silva, H.C.A
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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G.P.319
Comim, C.M, Mendonça, B.P, Dominguini, D, Vainzof, M, Streck, E.L, Dal-Pizzol, F, Quevedo, J
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Differential Expression of Genes Involved in the Degeneration and Regeneration Pathways in Mouse Models for Muscular Dystrophies
Onofre-Oliveira, P. C. G., Santos, A. L. F., Martins, P. M., Ayub-Guerrieri, D., Vainzof, M.
Published in Neuromolecular medicine (01.03.2012)
Published in Neuromolecular medicine (01.03.2012)
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Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
Nigro, V, de Sá Moreira, E, Piluso, G, Vainzof, M, Belsito, A, Politano, L, Puca, A A, Passos-Bueno, M R, Zatz, M
Published in Nature genetics (01.10.1996)
Published in Nature genetics (01.10.1996)
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P.20.10 Human adipose mesenchymal stem-cells injections in golden retriever muscular dystrophy (GRMD) dogs: a four-year follow-up
Zatz, M, Vieira, N, Secco, M, Zucconi, E, Valadares, M, Bueno, C.R, Vainzof, M, Gomes, J, Landini, V, Andrade, T
Published in Neuromuscular disorders : NMD (01.10.2013)
Published in Neuromuscular disorders : NMD (01.10.2013)
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