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Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2.
Fogel BL, Cho E, Wahnich A, Gao F, Becherel OJ, Wang X, Fike F, Chen L, Criscuolo C, De Michele G, Filla A, Collins A, Hahn AF, Gatti RA, Konopka G, Perlman S, Lavin MF, Geschwind DH, Coppola G. Fogel BL, et al. Among authors: filla a. Hum Mol Genet. 2014 Sep 15;23(18):4758-69. doi: 10.1093/hmg/ddu190. Epub 2014 Apr 23. Hum Mol Genet. 2014. PMID: 24760770 Free PMC article.
Friedreich's disease. A linkage study in southern and central Italy.
Cavalcanti F, Cocozza S, Filla A, De Michele G, Pianese L, Porcellini A, Monticelli A, Pandolfo M, Banfi S, Varrone S, et al. Cavalcanti F, et al. Among authors: filla a. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):519-23. Acta Neurol (Napoli). 1992. PMID: 1363458
Cerebellar ataxia and hypogonadism. A clinicopathological report.
De Michele G, Filla A, D'Armiento FP, Striano S, Barbieri F, Salvatore G, Di Carlo V, Mansi D. De Michele G, et al. Among authors: filla a. Clin Neurol Neurosurg. 1990;92(1):67-70. doi: 10.1016/0303-8467(90)90010-3. Clin Neurol Neurosurg. 1990. PMID: 2154358
340 results