Citation: E. Orlandi et al., Isolated hyperferritinemia with normal transferrin saturation and dysmetabolism, in the absence of the two known mutations in the HFE gene of hereditary hemochromatosis, HAEMATOLOG, 84(2), 1999, pp. 181-182
Authors:
Rampino, T
Arbustini, E
Gregorini, M
Guallini, P
Libetta, C
Maggio, M
Ranghino, A
Silini, E
Soccio, G
Dal Canton, A
Citation: T. Rampino et al., Hemodialysis prevents liver disease caused by hepatitis C virus: Role of hepatocyte growth factor, KIDNEY INT, 56(6), 1999, pp. 2286-2291
Authors:
Narula, J
Pandey, P
Arbustini, E
Haider, N
Narula, N
Kolodgie, FD
Dal Bello, B
Semigran, MJ
Bielsa-Masdeu, A
Dec, GW
Israels, S
Ballester, M
Virmani, R
Saxena, S
Kharbanda, S
Citation: J. Narula et al., Apoptosis in heart failure: Release of cytochrome c from mitochondria and activation of caspase-3 in human cardiomyopathy, P NAS US, 96(14), 1999, pp. 8144-8149
Authors:
Obici, L
Bellotti, V
Mangione, P
Stoppini, M
Arbustini, E
Verga, L
Zorzoli, I
Anesi, E
Zanotti, G
Campana, C
Vigano, M
Merlini, G
Citation: L. Obici et al., The new apolipoprotein A-I variant Leu(174) -> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide, AM J PATH, 155(3), 1999, pp. 695-702
Authors:
Arbustini, E
Fasani, R
Morbini, P
Diegoli, M
Grasso, M
Dal Bello, B
Marangoni, E
Banfi, P
Banchieri, N
Bellini, O
Comi, G
Narula, J
Campana, C
Gavazzi, A
Danesino, C
Vigano, M
Citation: E. Arbustini et al., Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure, HEART, 80(6), 1998, pp. 548-558
Authors:
Maghnie, M
Genovese, E
Sommaruga, MG
Arico, M
Locatelli, D
Arbustini, E
Pezzotta, S
Severi, F
Citation: M. Maghnie et al., Evolution of childhood central diabetes insipidus into panhypopituitarism with a large hypothalamic mass: is 'lymphocytic infundibuloneurohypophysitis' in children a different entity?, EUR J ENDOC, 139(6), 1998, pp. 635-640
Authors:
Noris, P
Arbustini, E
Spedini, P
Belletti, S
Balduini, CL
Citation: P. Noris et al., A new variant of Bernard-Soulier syndrome characterized by dysfunctional glycoprotein (GP) Ib and severely reduced amounts of GPIX and GPV, BR J HAEM, 103(4), 1998, pp. 1004-1013