Authors:
Romano, V
Lio, D
Cali, F
Scola, L
Leggio, L
D'Anna, C
De Leo, G
Salerno, A
Citation: V. Romano et al., A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemia, MOL CELL PR, 15(1), 2001, pp. 13-19
Authors:
Giannattasio, S
Dianzani, I
Lattanzio, P
Spada, M
Romano, V
Cali, F
Andria, G
Ponzone, A
Marra, E
Piazza, A
Citation: S. Giannattasio et al., Genetic heterogeneity in five Italian regions: Analysis of PAH mutations and minihaplotypes, HUMAN HERED, 52(3), 2001, pp. 154-159
Authors:
Puglisi-Allegra, S
Cabib, S
Pascucci, T
Ventura, R
Cali, F
Romano, V
Citation: S. Puglisi-allegra et al., Dramatic brain aminergic deficit in a genetic mouse model of phenylketonuria, NEUROREPORT, 11(6), 2000, pp. 1361-1364
Citation: F. Cali et al., IEEE 802.11 protocol: Design and performance evaluation of an adaptive backoff mechanism, IEEE J SEL, 18(9), 2000, pp. 1774-1786
Authors:
Bajardi, G
Ricevuto, G
Mastrandrea, G
Branca, M
Rinaudo, G
Cali, F
Diliberti, S
Lo Biundo, N
Asti, V
Citation: G. Bajardi et al., Surgical treatment of morbid obesity with biliopancreatic diversion and gastric banding: report on an 8-year experience involving 235 cases, ANN CHIR, 125(2), 2000, pp. 155-162
Authors:
Richards, M
Macaulay, V
Hickey, E
Vega, E
Sykes, B
Guida, V
Rengo, C
Sellitto, D
Cruciani, F
Kivisild, T
Villems, R
Thomas, M
Rychkov, S
Rychkov, O
Rychkov, Y
Golge, M
Dimitrov, D
Hill, E
Bradley, D
Romano, V
Cali, F
Vona, G
Demaine, A
Papiha, S
Triantaphyllidis, C
Stefanescu, G
Hatina, J
Belledi, M
Di Rienzo, A
Novelletto, A
Oppenheim, A
Norby, S
Al-Zaheri, N
Santachiara-Benerecetti, S
Scozzari, R
Torroni, A
Bandelt, HJ
Citation: M. Richards et al., Tracing European founder lineages in the near eastern mtDNA pool, AM J HU GEN, 67(5), 2000, pp. 1251-1276
Authors:
Corsello, G
Bosco, P
Cali, F
Cammarata, GM
Ciaccio, M
Piccione, M
Romano, V
Citation: G. Corsello et al., Maternal phenylketomuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L), EUR J PED, 158(1), 1999, pp. 83-84