Articles dans des revues avec comité de lecture (262)
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Eoli, M., Pandolfo, M., Milanese, C., Gasparini, P., Salmaggi, A., & Zeviani, M. (1994). The myelin basic protein gene is not a major susceptibility locus for multiple sclerosis in Italian patients. Journal of neurology, 241(10), 615-619.242.
Pandolfo, M., Pizzuti, A., Redolfi, E. M., Munaro, M., di Donato, S., Cavalcanti, F., Filla, A., Monticelli, A., Pianese, L., & Cocozza, S. (1994). Isolation of a new gene in the Friedreich ataxia candidate region on human chromosome 9 by cDNA direct selection. Biochemical medicine and metabolic biology, 52(2), 115-119.243.
Carella, F., Ciano, C., Pandolfo, M., Giovannini, P., Girotti, F., & Caraceni, T. (1994). Spasmodic dystonic laterocollis in familial cerebellar ataxia. Italian journal of neurological sciences, 15(5), 245-248.244.
Monrós, E., Smeyers, P., Rodius, F., Cañizares, J., Moltó, M. D., Vilchez, J. J., Pandolfo, M., Lopez-Arlandis, J., de Frutos, R., & Prieto, F. (1994). Mapping of Friedreich's ataxia locus by identification of recombination events in patients homozygous by descent. European journal of human genetics, 2(4), 291-299.245.
Sirugo, G., Duclos, F., Fujita, R., Keats, J. B., Pandolfo, M., Mandel, J. L., & Koenig, M. (1994). Mapping the Friedreich ataxia locus (FRDA) by linkage disequilibrium analysis with highly polymorphic microsatellites. Biomedicine & pharmacotherapy, 48(5-6), 219-224.246.
Jodice, C., Frontali, M., Persichetti, F., Novelletto, A., Pandolfo, M., Spadaro, M., Giunti, P., Schinaia, G., Lulli, P., & Malaspina, P. (1993). The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. Human molecular genetics, 2(9), 1383-1387.247.
Pandolfo, M., Munaro, M., Cocozza, S., Redolfi, E. M., Pianese, L., Cavalcanti, F., Monticelli, A., & di Donato, S. (1993). A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1. Human molecular genetics, 2(6), 822.248.
Verderio, E., Cavadini, P., Pandolfo, M., Didonato, S., & Taroni, F. (1993). Two novel sequence polymorphisms of the human carnitine palmitoyltransferase II (CPT1) gene. Human molecular genetics, 2(3), 334.249.
Lehesjoki, A.-E., Koskiniemi, M., Pandolfo, M., Antonelli, A., Kyllerman, M., Wahlström, J., Nergårdh, A., Burmeister, M., Sistonen, P., & Norio, R. (1992). Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseases. Neurology, 42(8), 1545-1550.251.
Cavalcanti, F., Cocozza, S., Filla, A., De Michele, G., Pianese, L., Porcellini, A., Monticelli, A., Pandolfo, M., Banfi, S., & Varrone, S. (1992). Friedreich's disease. A linkage study in southern and central Italy. Acta Neurologica, 14(4-6), 519-523.252.
Raimondi, E., Bernasconi, P., Moralli, D., Fujita, R., Uziel, G., di Donato, S., De Carli, L., & Pandolfo, M. (1991). Localization of DNA probes tightly linked to the Friedreich's ataxia locus by in situ hybridization in a case of pericentric inversion of chromosome 9. Human genetics, 86(5), 525-528.