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

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

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

Real time PCR quantification of frataxin mRNA in the peripheral blood leucocytes of Friedreich ataxia patients and carriers

Por Pianese, L, Turano, M, Lo, C, De Biase, I, Giacchetti, M, Monticelli, A, Criscuolo, C, Filla, A, Cocozza, S
Publicado em 2004

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

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