Search Results - "Galera, M.F."

Including analysis of acid alpha glucosidase in screening for muscle disease in Cuiabá, Brazil by Silva, R.C, Landim, P.O.L, Siqueira, H.H, Gumiero, B.R, Galera, M.F, Dalbem, J.S, Nishimyaka, A.N

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Mucolipidosis II and III alpha/beta in Brazil: Analysis of the GNPTAB gene by Cury, G.K., Matte, U., Artigalás, O., Alegra, T., Velho, R.V., Sperb, F., Burin, M.G., Ribeiro, E.M., Lourenço, C.M., Kim, C.A., Valadares, E.R., Galera, M.F., Acosta, A.X., Schwartz, I.V.D.

“…Mucolipidosis II and III (MLII and MLIII) alpha/beta are rare autosomal recessive lysosomal storage diseases (LSDs) caused by pathogenic variations in the…”
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Refractory epilepsy and other neurological manifestations of Schinzel-Gieidion syndrome by Landim, P.O.L, Silva Junior, R.C, Leitzke, L, Lima, S.L, Siqueira, H.H, Galera, M.F, Prates, M.T, Dalbem, J.S, Dos Reis, E.B.S, Campos, D.C.V

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P3.56 Analysis of the screening process for Pompe disease at theCuiabá University Teaching Hospital, Brazil in 2010 by Siqueira, H.H, Felicio, T.A, Borges, R.S, Lima, F.B, Galera, M.F, Dalbem, J.S

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