Filla A - Search Results

1

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.

Tezenas du Montcel S, Durr A, Bauer P, Figueroa KP, Ichikawa Y, Brussino A, Forlani S, Rakowicz M, Schöls L, Mariotti C, van de Warrenburg BP, Orsi L, Giunti P, Filla A, Szymanski S, Klockgether T, Berciano J, Pandolfo M, Boesch S, Melegh B, Timmann D, Mandich P, Camuzat A; Clinical Research Consortium for Spinocerebellar Ataxia (CRC-SCA); EUROSCA network; Goto J, Ashizawa T, Cazeneuve C, Tsuji S, Pulst SM, Brusco A, Riess O, Brice A, Stevanin G. Tezenas du Montcel S, et al. Among authors: filla a. Brain. 2014 Sep;137(Pt 9):2444-55. doi: 10.1093/brain/awu174. Epub 2014 Jun 26. Brain. 2014. PMID: 24972706 Free PMC article.

2

Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes.

Filla A, De Michele G, Cavalcanti F, Perretti A, Santoro L, Barbieri F, D'Arienzo G, Campanella G. Filla A, et al. J Neurol Neurosurg Psychiatry. 1990 Aug;53(8):667-70. doi: 10.1136/jnnp.53.8.667. J Neurol Neurosurg Psychiatry. 1990. PMID: 2213043 Free PMC article.

3

Late onset recessive ataxia with Friedreich's disease phenotype.

De Michele G, Filla A, Barbieri F, Perretti A, Santoro L, Trombetta L, Santorelli F, Campanella G. De Michele G, et al. Among authors: filla a. J Neurol Neurosurg Psychiatry. 1989 Dec;52(12):1398-401. doi: 10.1136/jnnp.52.12.1398. J Neurol Neurosurg Psychiatry. 1989. PMID: 2614435 Free PMC article.

4

Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.

Filla A, De Michele G, Banfi S, Santoro L, Perretti A, Cavalcanti F, Pianese L, Castaldo I, Barbieri F, Campanella G, et al. Filla A, et al. Neurology. 1995 Apr;45(4):793-6. doi: 10.1212/wnl.45.4.793. Neurology. 1995. PMID: 7723972

5

Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneity.

Sirugo G, Cocozza S, Brice A, Cavalcanti F, De Michele G, Dones I, Filla A, Koenig M, Lorenzetti D, Monticelli A, et al. Sirugo G, et al. Among authors: filla a. Eur J Hum Genet. 1993;1(2):133-43. doi: 10.1159/000472400. Eur J Hum Genet. 1993. PMID: 7914465

6

Age of onset, sex, and cardiomyopathy as predictors of disability and survival in Friedreich's disease: a retrospective study on 119 patients.

De Michele G, Perrone F, Filla A, Mirante E, Giordano M, De Placido S, Campanella G. De Michele G, et al. Among authors: filla a. Neurology. 1996 Nov;47(5):1260-4. doi: 10.1212/wnl.47.5.1260. Neurology. 1996. PMID: 8909440

7

Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia.

Ragno M, De Michele G, Cavalcanti F, Pianese L, Monticelli A, Curatola L, Bollettini F, Cocozza S, Caruso G, Santoro L, Filla A. Ragno M, et al. Among authors: filla a. Neurology. 1997 Dec;49(6):1617-20. doi: 10.1212/wnl.49.6.1617. Neurology. 1997. PMID: 9409356

8

Determinants of onset age in Friedreich's ataxia.

De Michele G, Filla A, Criscuolo C, Scarano V, Cavalcanti F, Pianese L, Monticelli A, Cocozza S. De Michele G, et al. Among authors: filla a. J Neurol. 1998 Mar;245(3):166-8. doi: 10.1007/s004150050198. J Neurol. 1998. PMID: 9553847

9

Cerebral blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients.

De Michele G, Mainenti PP, Soricelli A, Di Salle F, Salvatore E, Longobardi MR, Postiglione A, Salvatore M, Filla A. De Michele G, et al. Among authors: filla a. J Neurol. 1998 Sep;245(9):603-8. doi: 10.1007/s004150050253. J Neurol. 1998. PMID: 9758299

10

Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich's ataxia.

Santoro L, De Michele G, Perretti A, Crisci C, Cocozza S, Cavalcanti F, Ragno M, Monticelli A, Filla A, Caruso G. Santoro L, et al. Among authors: filla a. J Neurol Neurosurg Psychiatry. 1999 Jan;66(1):93-6. doi: 10.1136/jnnp.66.1.93. J Neurol Neurosurg Psychiatry. 1999. PMID: 9886462 Free PMC article.

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