Articles dans des revues avec comité de lecture (262)

  1. 241. 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.
  2. 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.
  3. 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.
  4. 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.
  5. 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.
  6. 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.
  7. 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.
  8. 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.
  9. 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.
  10. 250. Pandolfo, M. (1992). A rapid method to isolate (GT)n repeats from yeast artificial chromosomes. Nucleic acids research, 20(5), 1154.
  11. 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.
  12. 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.

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