Early ficolin-1 is a sensitive prognostic marker for functional outcome in ischemic stroke von Zangari, R, Zanier, E R, Torgano, G, Bersano, A, Beretta, S, Beghi, E, Casolla, B, Checcarelli, N, Lanfranconi, S, Maino, A, Mandelli, C, Micieli, G, Orzi, F, Picetti, E, Silvestrini, M, Stocchetti, N, Zecca, B, Garred, P, De Simoni, M G

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Endovascular Treatment for Acute Ischemic Stroke von Ciccone, Alfonso, Valvassori, Luca, Nichelatti, Michele, Sgoifo, Annalisa, Ponzio, Michela, Sterzi, Roberto, Boccardi, Edoardo

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Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2 von Sue, C. M., Karadimas, C., Checcarelli, N., Tanji, K., Papadopoulou, L. C., Pallotti, F., Guo, F. L., Shanske, S., Hirano, M., De Vivo, D. C., Van Coster, R., Kaplan, P., Bonilla, E., DiMauro, S.

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Measurement of ATP production in mitochondrial disorders von Shepherd, R. K., Checcarelli, N., Naini, A., De Vivo, D. C., DiMauro, S., Sue, C. M.

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Mitochondrial DNA abnormalities and autistic spectrum disorders von Pons, Roser, Andreu, Antoni L., Checcarelli, Nicoletta, Vilà, Maya R., Engelstad, Kristin, Sue, Carolyn M., Shungu, Dikoma, Haggerty, Rita, De Vivo, Darryl C., DiMauro, Salvatore

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A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy von ANDREU, A. L, CHECCARELLI, N, IWATA, S, SHANSKE, S, DIMAURO, S

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Intra-arterial or intravenous thrombolysis for acute ischemic stroke? The SYNTHESIS pilot trial von Ciccone, A, Valvassori, L, Ponzio, M, Ballabio, E, Gasparotti, R, Sessa, M, Scomazzoni, F, Tiraboschi, P, Sterzi, R

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Desmin and vimentin as markers of regeneration in muscle diseases von GALLANTI, A, PRELLE, A, MOGGIO, M, CISCATO, P, CHECCARELLI, N, SCIACCO, M, COMINI, A, SCARLATO, G

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Mitochondrial myopathy : correlation between oxidative defect and mitochondrial DNA deletions at single fiber level von PRELLE, A, FAGIOLARI, G, CHECCARELLI, N, MOGGIO, M, BATTISTEL, A, COMI, G. P, BAZZI, P, BORDONI, A, ZEVIANI, M, SCARLATO, G

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Multiple sclerosis and mitochondrial myopathy : an unusual combination of diseases von BET, L, MOGGIO, M, COMI, G. P, MARIANI, C, PRELLE, A, CHECCARELLI, N, BORDONI, A, BRESOLIN, N, SCARPINI, E, SCARLATO, G

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Congenital myopathy associated with abnormal accumulation of desmin and dystrophin von Prelle, A., Moggio, M., Comi, G.P., Gallanti, A., Checcarelli, N., Bresolin, N., Ciscato, P., Fortunato, F., Scarlato, G.

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Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation von Giordano, Carla, Pallotti, Francesco, Walker, Winsome F, Checcarelli, Nicoletta, Musumeci, Olimpia, Santorelli, Filippo, d'Amati, Giulia, Schon, Eric A, DiMauro, Salvatore, Hirano, Michio, Davidson, Mercy M

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Appearance and localization of dystrophin in normal human fetal muscle von Prelle, A., Chianese, L., Moggio, M., Gallanti, A., Sciacco, M., Checcarelli, N., Comi, G., Scarpini, E., Bonilla, E., Scarlato, G.

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Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy von Checcarelli, Nicoletta, Prelle, Allessandro, Moggio, Maurizio, Comi, Giacomo, Bresolin, Nereo, Papadimitriou, Alex, Fagiolari, Gigliola, Bordoni, Andreina, Scarlato, Guglielmo

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Differential features of patients with mutations in two COX assembly genes,SURF-1 andSCO2 von Sue, C. M., Karadimas, C., Checcarelli, N., Tanji, K., Papadopoulou, L. C., Pallotti, F., Guo, F. L., Shanske, S., Hirano, M., De Vivo, D. C., Van Coster, R., Kaplan, P., Bonilla, E., DiMauro, S.

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Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis von Prelle, Alessandro, Moggio, Maurizio, Checcarelli, Nicoletta, Comi, Giacomo, Bresolin, Nereo, Battistel, Alessandro, Bordoni, Andreina, Scarlato, Guglielmo

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Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy von Moggio, Maurizio, Prelle, Alessandro, Fagiolari, Gigliola, Checcarelli, Nicoletta, Sciacco, Monica, Ciscato, Patrizia, Scarlato, Guglielmo

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Additional file 2: Table S2.1. of Early ficolin-1 is a sensitive prognostic marker for functional outcome in ischemic stroke von R. Zangari, E. Zanier, G. Torgano, A. Bersano, S. Beretta, E. Beghi, B. Casolla, N. Checcarelli, S. Lanfranconi, A. Maino, C. Mandelli, G. Micieli, F. Orzi, E. Picetti, M. Silvestrini, N. Stocchetti, B. Zecca, P. Garred, M. De Simoni

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Additional file 4: Table S4. of Early ficolin-1 is a sensitive prognostic marker for functional outcome in ischemic stroke von R. Zangari, E. Zanier, G. Torgano, A. Bersano, S. Beretta, E. Beghi, B. Casolla, N. Checcarelli, S. Lanfranconi, A. Maino, C. Mandelli, G. Micieli, F. Orzi, E. Picetti, M. Silvestrini, N. Stocchetti, B. Zecca, P. Garred, M. De Simoni

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Additional file 1: Table S1. of Early ficolin-1 is a sensitive prognostic marker for functional outcome in ischemic stroke von R. Zangari, E. Zanier, G. Torgano, A. Bersano, S. Beretta, E. Beghi, B. Casolla, N. Checcarelli, S. Lanfranconi, A. Maino, C. Mandelli, G. Micieli, F. Orzi, E. Picetti, M. Silvestrini, N. Stocchetti, B. Zecca, P. Garred, M. De Simoni

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