AAAAAA
Results:
1-12
|
Results: 12
Authors:
Persico, AM
D'Agruma, L
Maiorano, N
Totaro, A
Militerni, R
Bravaccio, C
Wassink, TH
Schneider, C
Melmed, R
Trillo, S
Montecchi, F
Palermo, M
Pascucci, T
Puglisi-Allegra, S
Reichelt, KL
Conciatori, M
Marino, R
Quattrocchi, CC
Baldi, A
Zelante, L
Gasparini, P
Keller, F
Citation: Am. Persico et al., Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder, MOL PSYCHI, 6(2), 2001, pp. 150-159
Authors:
Montosi, G
Donovan, A
Totaro, A
Garuti, C
Pignatti, E
Cassanelli, S
Trenor, CC
Gasparini, P
Andrews, NC
Pietrangelo, A
Citation: G. Montosi et al., Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene, J CLIN INV, 108(4), 2001, pp. 619-623
Authors:
Roetto, A
Totaro, A
Piperno, A
Piga, A
Longo, F
Garozzo, G
Cali, A
De Gobbi, M
Gasparini, P
Camaschella, C
Citation: A. Roetto et al., New mutations inactivating transferrin receptor 2 in hemochromatosis type 3, BLOOD, 97(9), 2001, pp. 2555-2560
Authors:
Roetto, A
Alberti, F
Daraio, F
Cali, A
Cazzola, M
Totaro, A
Gasparini, P
Camaschella, C
Citation: A. Roetto et al., Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21, BL CELL M D, 26(3), 2000, pp. 205-210
Authors:
Camaschella, C
Roetto, A
Cali, A
De Gobbi, M
Garozzo, G
Carella, M
Majorano, N
Totaro, A
Gasparini, P
Citation: C. Camaschella et al., The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22, NAT GENET, 25(1), 2000, pp. 14-15
Authors:
Iolascon, A
Servedio, V
Carbone, R
Totaro, A
Carella, M
Perrotta, S
Wickramasinghe, SN
Delaunay, J
Heimpel, H
Gasparini, P
Citation: A. Iolascon et al., Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?, HAEMATOLOG, 85(5), 2000, pp. 470-474
Authors:
Margaglione, M
Di Castelnuovo, A
Totaro, A
Iacoviello, L
Di Minno, G
Citation: M. Margaglione et al., Risk of myocardial infarction in carriers of mutations in the hemochromatosis-associated gene, THROMB HAEM, 84(4), 2000, pp. 726-727
Authors:
Angius, A
Spinelli, P
Ghilotti, G
Casu, G
Sole, G
Loi, A
Totaro, A
Zelante, L
Gasparini, P
Orzalesi, N
Piratsu, M
Bonomi, L
Citation: A. Angius et al., Myocilin Gln368stop mutation and advanced age as risk factors for late-onset primary open-angle glaucoma, ARCH OPHTH, 118(5), 2000, pp. 674-679
Authors:
Merryweather-Clarke, AT
Pointon, JJ
Shearman, JD
Robson, KJH
Jouanolle, AM
Mosser, A
David, V
Le Gall, JY
Halsall, DJ
Elsey, TS
Kelly, A
Cox, TM
Clare, M
Bomford, A
Vandwalle, JL
Rochette, J
Borot, N
Coppin, H
Roth, MP
Ryan, E
Crowe, J
Totaro, A
Gasparini, P
Roetto, A
Gamaschella, C
Darke, C
Wallace, DF
Saeb-Parsy, K
Dooley, JS
Worwood, M
Walker, AP
Citation: At. Merryweather-clarke et al., Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results, NAT GENET, 23(3), 1999, pp. 271-271
Authors:
Pietrangelo, A
Montosi, G
Totaro, A
Garuti, C
Conte, D
Cassanelli, S
Fraquelli, M
Sardini, C
Vasta, F
Gasparini, P
Citation: A. Pietrangelo et al., Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene, N ENG J MED, 341(10), 1999, pp. 725-732
Authors:
Savoia, A
Del Vecchio, M
Totaro, A
Perrotta, S
Amendola, G
Moretti, A
Zelante, L
Iolascon, A
Citation: A. Savoia et al., An autosomal dominant thrombocytopenia gene maps to chromosomal region 10p, AM J HU GEN, 65(5), 1999, pp. 1401-1405
Authors:
Roetto, A
Totaro, A
Cazzola, M
Cicilano, M
Bosio, S
D'Ascola, G
Carella, M
Zelante, L
Kelly, AL
Cox, TM
Gasparini, P
Camaschella, C
Citation: A. Roetto et al., Juvenile hemochromatosis locus maps to chromosome 1q, AM J HU GEN, 64(5), 1999, pp. 1388-1393
Risultati:
1-12
|