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Nigrostriatal involvement in ataxia with oculomotor apraxia type 1.
Salvatore E, Varrone A, Criscuolo C, Mancini P, Sansone V, Strisciuglio C, Cicala D, Scarano V, Salvatore M, Pappatà S, De Michele G, Filla A. Salvatore E, et al. Among authors: mancini p. J Neurol. 2008 Jan;255(1):45-8. doi: 10.1007/s00415-007-0657-x. Epub 2007 Nov 21. J Neurol. 2008. PMID: 18004640
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.
Criscuolo C, Chessa L, Di Giandomenico S, Mancini P, Saccà F, Grieco GS, Piane M, Barbieri F, De Michele G, Banfi S, Pierelli F, Rizzuto N, Santorelli FM, Gallosti L, Filla A, Casali C. Criscuolo C, et al. Among authors: mancini p. Neurology. 2006 Apr 25;66(8):1207-10. doi: 10.1212/01.wnl.0000208402.10512.4a. Neurology. 2006. PMID: 16636238
Very late onset in ataxia oculomotor apraxia type I.
Criscuolo C, Mancini P, Menchise V, Saccà F, De Michele G, Banfi S, Filla A. Criscuolo C, et al. Among authors: mancini p. Ann Neurol. 2005 May;57(5):777. doi: 10.1002/ana.20463. Ann Neurol. 2005. PMID: 15852392 Free article. No abstract available.
Screening for POLG1 mutations in a Southern Italian ataxia population.
Criscuolo C, Mancini P, Ammendola S, Cicala D, Banfi S, De Michele G, Filla A. Criscuolo C, et al. Among authors: mancini p. J Neurol. 2008 Mar;255(3):454-5. doi: 10.1007/s00415-007-0736-z. Epub 2007 Dec 19. J Neurol. 2008. PMID: 18080848 No abstract available.
430 results