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Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease.
Martinez M, Brice A, Vaughan JR, Zimprich A, Breteler MM, Meco G, Filla A, Farrer MJ, Bétard C, Singleton A, Hardy J, De Michele G, Bonifati V, Oostra BA, Gasser T, Wood NW, Dürr A. Martinez M, et al. Among authors: filla a. Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):72-4. doi: 10.1002/ajmg.b.30196. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15924299
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
Paternal preponderance in familial Parkinson's disease.
Campanella G, Idone M, De Michele G, Filla A. Campanella G, et al. Among authors: filla a. Neurology. 1984 Oct;34(10):1398-400. doi: 10.1212/wnl.34.10.1398-b. Neurology. 1984. PMID: 6541322 No abstract available.
A genetic study of Parkinson's disease.
De Michele G, Filla A, Marconi R, Volpe G, D'Alessio A, Scala R, Ambrosio G, Campanella G. De Michele G, et al. Among authors: filla a. J Neural Transm Suppl. 1995;45:21-5. J Neural Transm Suppl. 1995. PMID: 8748605
Genetic abnormalities in Friedreich's ataxia.
Filla A, De Michele G, Cocozza S. Filla A, et al. N Engl J Med. 1997 Apr 3;336(14):1021-2; author reply 1022. N Engl J Med. 1997. PMID: 9091786 No abstract available.
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Tassin J, Dürr A, de Broucker T, Abbas N, Bonifati V, De Michele G, Bonnet AM, Broussolle E, Pollak P, Vidailhet M, De Mari M, Marconi R, Medjbeur S, Filla A, Meco G, Agid Y, Brice A. Tassin J, et al. Among authors: filla a. Am J Hum Genet. 1998 Jul;63(1):88-94. doi: 10.1086/301934. Am J Hum Genet. 1998. PMID: 9634531 Free PMC article.
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
Cossée M, Dürr A, Schmitt M, Dahl N, Trouillas P, Allinson P, Kostrzewa M, Nivelon-Chevallier A, Gustavson KH, Kohlschütter A, Müller U, Mandel JL, Brice A, Koenig M, Cavalcanti F, Tammaro A, De Michele G, Filla A, Cocozza S, Labuda M, Montermini L, Poirier J, Pandolfo M. Cossée M, et al. Among authors: filla a. Ann Neurol. 1999 Feb;45(2):200-6. doi: 10.1002/1531-8249(199902)45:2<200::aid-ana10>3.0.co;2-u. Ann Neurol. 1999. PMID: 9989622
336 results