Idiopathic cerebellar ataxia associated with celiac disease: lack of distinctive neurological features

Por Pellecchia, M. T., Scala, R., Filla, A., De Michele, G., Ciacci, C., Barone, P.
Publicado em 1999

The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.

Por Filla, A., De Michele, G., Cavalcanti, F., Pianese, L., Monticelli, A., Campanella, G., Cocozza, S.
Publicado em 1996

Late onset recessive ataxia with Friedreich's disease phenotype.

Por De Michele, G, Filla, A, Barbieri, F, Perretti, A, Santoro, L, Trombetta, L, Santorelli, F, Campanella, G
Publicado em 1989

Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype

Por Giacchetti, M, Monticelli, A, De Biase, I, Pianese, L, Turano, M, Filla, A, De Michele, G, Cocozza, S
Publicado em 2004

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

Por Filla, A, De Michele, G, Cavalcanti, F, Perretti, A, Santoro, L, Barbieri, F, D'Arienzo, G, Campanella, G
Publicado em 1990

The effect of parental gender on the GAA dynamic mutation in the FRDA gene.

Por Pianese, L, Cavalcanti, F, De Michele, G, Filla, A, Campanella, G, Calabrese, O, Castaldo, I, Monticelli, A, Cocozza, S
Publicado em 1997

Idiopathic cerebellar ataxia associated with celiac disease: lack of distinctive neurological features

Por HADJIVASSILIOU, M, GRUNEWALD, R, DAVIES-JONES, G, PELLECCHIA, M, SCALA, R, FILLA, A, DE MICHELE, G, BARONE, P
Publicado em 1999

Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.

Por Pianese, L, Cocozza, S, Campanella, G, Castaldo, I, Cavalcanti, F, De Michele, G, Filla, A, Monticelli, A, Munaro, M, Redolfi, E
Publicado em 1994

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

Por Santoro, L, De Michele, G, Perretti, A, Crisci, C, Cocozza, S, Cavalcanti, F, Ragno, M, Monticelli, A, Filla, A, Caruso, G
Publicado em 1999

Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.

Por De Michele, G, Filla, A, Cavalcanti, F, Di Maio, L, Pianese, L, Castaldo, I, Calabrese, O, Monticelli, A, Varrone, S, Campanella, G
Publicado em 1994

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.

Por De Michele, G, De Fusco, M, Cavalcanti, F, Filla, A, Marconi, R, Volpe, G, Monticelli, A, Ballabio, A, Casari, G, Cocozza, S
Publicado em 1998

Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy.

Por Seri, M, Cusano, R, Forabosco, P, Cinti, R, Caroli, F, Picco, P, Bini, R, Morra, V B, De Michele, G, Lerone, M, Silengo, M, Pela, I, Borrone, C, Romeo, G, Devoto, M
Publicado em 1999

Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease

Por Martinez, M, Brice, A, Vaughan, J, Zimprich, A, Breteler, M, Meco, G, Filla, A, Farrer, M, Betard, C, Hardy, J, De Michele, G, Bonifati, V, Oostra, B, Gasser, T, Wood, N, Durr, A, the, F
Publicado em 2004

The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations

Por Sharma, M, Mueller, J C, Zimprich, A, Lichtner, P, Hofer, A, Leitner, P, Maass, S, Berg, D, Dürr, A, Bonifati, V, De Michele, G, Oostra, B, Brice, A, Wood, N W, Muller‐Myhsok, B, Gasser, T
Publicado em 2006

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...

Por Tassin, J, Dürr, A, de Broucker, T, Abbas, N, Bonifati, V, De Michele, G, Bonnet, A M, Broussolle, E, Pollak, P, Vidailhet, M, De Mari, M, Marconi, R, Medjbeur, S, Filla, A, Meco, G, Agid, Y, Brice, A
Publicado em 1998