Search Results - Checcarelli, N

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  1. 1
    Early ficolin-1 is a sensitive prognostic marker for functional outcome in ischemic stroke

    Early ficolin-1 is a sensitive prognostic marker for functional outcome in ischemic stroke by 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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  2. 2
    Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2

    Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2 by 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.

    Published in Annals of neurology
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  3. 3
    Measurement of ATP production in mitochondrial disorders

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

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  4. 4
    Mitochondrial DNA abnormalities and autistic spectrum disorders

    Mitochondrial DNA abnormalities and autistic spectrum disorders by 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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  5. 5
    Desmin and vimentin as markers of regeneration in muscle diseases

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

    Published in Acta neuropathologica
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  6. 6
    Mitochondrial myopathy : correlation between oxidative defect and mitochondrial DNA deletions at single fiber level

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

    Published in Acta neuropathologica
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  7. 7
    Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation

    Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation by 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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  8. 8
    Differential features of patients with mutations in two COX assembly genes,SURF-1 andSCO2

    Differential features of patients with mutations in two COX assembly genes,SURF-1 andSCO2 by 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.

    Published in Annals of neurology
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