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Results:
1-7
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Results: 7
Authors:
Pirulli, D
Puzzer, D
De Fusco, M
Crovella, S
Amoroso, A
Scolari, F
Viola, BF
Maiorca, R
Caridi, G
Savoldi, S
Ghiggeri, G
Casari, G
Citation: D. Pirulli et al., Molecular analysis of uromodulin and SAH genes, positional candidates for autosomal dominant medullary cystic kidney disease linked to 16p12, J NEPHROL, 14(5), 2001, pp. 392-396
Authors:
Ahmad, W
Noci, S
Haque, MFU
Sarno, T
Aridon, P
Ahmad, MM
Amin-ud-din, M
Rafiq, MA
Haque, SU
De Fusco, M
Ballabio, A
Franco, B
Casari, G
Citation: W. Ahmad et al., Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family, AM J MED G, 100(1), 2001, pp. 62-65
Authors:
De Fusco, M
Becchetti, A
Patrignani, A
Annesi, G
Gambardella, A
Quattrone, A
Ballabio, A
Wanke, E
Casari, G
Citation: M. De Fusco et al., The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy, NAT GENET, 26(3), 2000, pp. 275-276
Authors:
Gambardella, A
Annesi, G
De Fusco, M
Patrignani, A
Aguglia, U
Annesi, F
Pasqua, AA
Spadafora, P
Oliveri, RL
Valentino, P
Zappia, M
Ballabio, A
Casari, G
Quattrone, A
Citation: A. Gambardella et al., A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps tochromosome 1, NEUROLOGY, 55(10), 2000, pp. 1467-1471
Authors:
Ahmad, W
De Fusco, M
ul Haque, MF
Aridon, P
Sarno, T
Sohail, M
ul Haque, S
Ahmad, M
Ballabio, A
Franco, B
Casari, G
Citation: W. Ahmad et al., Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity, EUR J HUM G, 7(7), 1999, pp. 828-832
Authors:
Guerrini, R
Bonanni, P
Nardocci, N
Parmeggiani, L
Piccirilli, M
De Fusco, M
Aridon, P
Ballabio, A
Carrozzo, R
Casari, G
Citation: R. Guerrini et al., Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: Delineation of the syndrome and gene mapping to chromosome 16p12-11.2, ANN NEUROL, 45(3), 1999, pp. 344-352
Authors:
Scolari, F
Puzzer, D
Amoroso, A
Caridi, G
Ghiggeri, GM
Maiorca, R
Aridon, P
De Fusco, M
Ballabio, A
Casari, G
Citation: F. Scolari et al., Identification of a new locus for medullary cystic disease, on chromosome 16p12, AM J HU GEN, 64(6), 1999, pp. 1655-1660
Risultati:
1-7
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