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Results:
1-13
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Results: 13
Authors:
Valente, EM
Bentivoglio, AR
Cassetta, E
Dixon, PH
Davis, MB
Ferraris, A
Ialongo, T
Frontali, M
Wood, NW
Albanese, A
Citation: Em. Valente et al., Identification of a novel primary torsion dystonia loons (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset, NEUROL SCI, 22(1), 2001, pp. 95-96
Authors:
Valente, EM
Bentivoglio, AR
Cassetta, E
Dixon, PH
Davis, MB
Ferraris, A
Ialongo, T
Frontali, M
Wood, NW
Albanese, A
Citation: Em. Valente et al., DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial cervical or upper limb onset, ANN NEUROL, 49(3), 2001, pp. 362-366
Authors:
Frontali, M
Citation: M. Frontali, Spinocerebellar ataxia type 6: Channelopathy or glutamine repeat disorder?, BRAIN RES B, 56(3-4), 2001, pp. 227-231
Authors:
Valente, EM
Bentivoglio, AR
Dixon, PH
Ferraris, A
Ialongo, T
Frontali, M
Albanese, A
Wood, NW
Citation: Em. Valente et al., Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36, AM J HU GEN, 68(4), 2001, pp. 895-900
Authors:
Guida, S
Trettel, F
Pagnutti, S
Mantuano, E
Tottene, A
Veneziano, L
Fellin, T
Spadaro, M
Stauderman, KA
Williams, ME
Volsen, S
Ophoff, RA
Frants, RR
Jodice, C
Frontali, M
Pietrobon, D
Citation: S. Guida et al., Complete loss of P/Q calcium channel activity caused by a CACNA1A missensemutation carried by patients with episodic ataxia type 2, AM J HU GEN, 68(3), 2001, pp. 759-764
Authors:
Stevanin, G
Herman, A
Durr, A
Jodice, C
Frontali, M
Agid, Y
Brice, A
Citation: G. Stevanin et al., Are (CTG)(n) expansions at the SCA8 locus rare polymorphisms?, NAT GENET, 24(3), 2000, pp. 213-213
Authors:
Trettel, F
Mantuano, E
Calabresi, V
Veneziano, L
Olsen, AS
Georgescu, A
Gordon, L
Sabbadini, G
Frontali, M
Jodice, C
Citation: F. Trettel et al., A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome, GENE, 241(1), 2000, pp. 45-50
Authors:
Albanese, A
Bentivoglio, AR
Del Grosso, N
Cassetta, E
Frontali, M
Valente, EM
Tonali, P
Citation: A. Albanese et al., Phenotype variability of dystonia in monozygotic twins, J NEUROL, 247(2), 2000, pp. 148-150
Authors:
Squitieri, F
Sabbadini, G
Mandich, P
Gellera, C
Di Maria, E
Bellone, E
Castellotti, B
Nargi, E
de Grazia, U
Frontali, M
Novelletto, A
Citation: F. Squitieri et al., Family and molecular data for a fine analysis of age at onset in Huntington disease, AM J MED G, 95(4), 2000, pp. 366-373
CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci
Authors:
Frontali, M
Novelletto, A
Annesi, G
Jodice, C
Citation: M. Frontali et al., CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci, PHI T ROY B, 354(1386), 1999, pp. 1089-1094
Authors:
Cassetta, E
Del Grosso, N
Bentivoglio, AR
Valente, EM
Frontali, M
Albanese, A
Citation: E. Cassetta et al., Italian family with cranial cervical dystonia: Clinical and genetic study, MOVEMENT D, 14(5), 1999, pp. 820-825
Authors:
Jarman, PR
del Grosso, N
Valente, EM
Leube, B
Cassetta, E
Bentivoglio, AR
Waddy, HM
Uitti, RJ
Maraganore, DM
Albanese, A
Frontali, M
Auburger, G
Bressman, SB
Wood, NW
Nygaard, TG
Citation: Pr. Jarman et al., Primary torsion dystonia: the search for genes is not over, J NE NE PSY, 67(3), 1999, pp. 395-397
Authors:
Trowsdale, J
Beck, S
Boyle, JM
Campbell, D
Cann, HM
Edwards, Y
Frontali, M
Galibert, F
Le Gall, JY
Nizetic, D",Pontarotti,"Ragoussis, J
Terrenato, L
Ziegler, A
Citation: J. Trowsdale et al., Physical Mapping of human chromosome 6, BIOM HLTH R, 23, 1998, pp. 101-115
Risultati:
1-13
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