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Results: 26-41/41
Authors:
Girodano, P
Micelli, M
Coppola, B
Trerotoli, P
De Lucia, D
Iolascon, A
Citation: P. Girodano et al., Analysis of three genetic polymorphisms as risk factors for thrombosis, INT J CL L, 29(4), 1999, pp. 174-175
Authors:
Iolascon, A
Faienza, MF
Giordani, L
Perrotta, S
Ruggiu, G
Meloni, GF
del Giudice, EM
Citation: A. Iolascon et al., Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome, EUR J HAEMA, 62(5), 1999, pp. 307-310
Authors:
Carella, M
Stewart, GW
Ajetunmobi, JF
Schettini, F
Delaunay, J
Iolascon, A
Citation: M. Carella et al., Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemia, HAEMATOLOG, 84(9), 1999, pp. 862-863
Authors:
Perrotta, S
Iolascon, A
Polito, R
d'Urzo, G
Conte, ML
del Giudice, EM
Citation: S. Perrotta et al., 4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis, HAEMATOLOG, 84(7), 1999, pp. 660-662
Authors:
Iolascon, A
Faienza, MF
Perrotta, S
Meloni, GF
Ruggiu, G
del Giudice, EM
Citation: A. Iolascon et al., Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates, HAEMATOLOG, 84(2), 1999, pp. 99-102
Authors:
Iolascon, A
Faienza, MF
Centra, M
Storelli, S
Zelante, L
Savoia, A
Citation: A. Iolascon et al., (TA)(8) allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome, HAEMATOLOG, 84(2), 1999, pp. 106-109
Authors:
Sampietro, M
Iolascon, A
Citation: M. Sampietro et A. Iolascon, Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes, HAEMATOLOG, 84(2), 1999, pp. 150-157
Authors:
Lo Cunsolo, C
Iolascon, A
Cavazzana, A
Cusano, R
Strigini, P
Mazzocco, K
Giordani, L
Massimo, L
De Bernardi, B
Conte, M
Tonini, GP
Citation: C. Lo Cunsolo et al., Neuroblastoma in two siblings supports the role of 1p36 deletion in tumor development, CANC GENET, 109(2), 1999, pp. 126-130
Authors:
Iolascon, A
Perrotta, S
Amendola, G
Altomare, M
Bagnara, GP
Del Vecchio, ME
Savoia, A
Citation: A. Iolascon et al., Familial dominant thrombocytopenia: Clinical, biologic, and molecular studies, PEDIAT RES, 46(5), 1999, pp. 548-552
Authors:
Bobba, A
Marra, E
Giannattasio, S
Iolascon, A
Monno, F
Di Maio, S
Citation: A. Bobba et al., 21-hydroxylase deficiency in Italy: a distinct distribution pattern of CYP21 mutations in a sample from southern Italy, J MED GENET, 36(8), 1999, pp. 648-650
Authors:
Beauchamp-Nicoud, A
Schischmanoff, PO
Alloisio, N
Boivin, P
Parsons, SF
Mielot, F
Tchernia, G
Legrand, A
del Giudice, EM
Gasparini, P
Iolascon, A
Wickramasinghe, SN
Delaunay, J
Citation: A. Beauchamp-nicoud et al., Suppression of CDA II expression in a homozygote, BR J HAEM, 106(4), 1999, pp. 948-953
Authors:
del Giudice, EM
Perrotta, S
Nobili, B
Specchia, C
d'Urzo, G
Iolascon, A
Citation: Em. Del Giudice et al., Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis, BLOOD, 94(7), 1999, pp. 2259-2262
Authors:
Iolascon, A
Stewart, GW
Ajetunmobi, JF
Perrotta, S
Delaunay, J
Carella, M
Zelante, L
Gasparini, P
Citation: A. Iolascon et al., Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis), BLOOD, 93(9), 1999, pp. 3120-3123
Authors:
Perrotta, S
Polito, R
Conte, ML
Nobili, B
Cutillo, S
del Giudice, EM
Nigro, V
Iolascon, A
Amendola, G
Citation: S. Perrotta et al., Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: Band 3 Vesuvio, BLOOD, 93(6), 1999, pp. 2131-2132
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:
Giordano, P
De Lucia, D
Coppola, B
Iolascon, A
Citation: P. Giordano et al., Homozygous prothrombin gene mutation and ischemic cerebrovascular disease, ACT HAEMAT, 102(2), 1999, pp. 101-103