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Results:
1-22
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Results: 22
Authors:
Papanikolaou, G
Politou, M
Roetto, A
Bosio, S
Sakelaropoulos, N
Camaschella, C
Loukopoulos, D
Citation: G. Papanikolaou et al., Linkage to chromosome 1q in Greek families with juvenile hemochromatosis, BL CELL M D, 27(4), 2001, pp. 744-749
Authors:
Bosio, S
Cavallero, G
Brusa, E
Alberti, F
Camaschella, C
Citation: S. Bosio et al., A new mutation trans to 1278T cystathionine beta-synthase associated with Factor V Leiden causes mild homocystinuria but severe vascular disease, THROMB HAEM, 86(2), 2001, pp. 716-717
Authors:
Girelli, D
Bozzini, C
Zecchina, G
Tinazzi, E
Bosio, S
Piperno, A
Ramenghi, U
Peters, J
Levi, S
Camaschella, C
Corrocher, R
Citation: D. Girelli et al., Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome, BR J HAEM, 115(2), 2001, pp. 334-340
Authors:
De Gobbi, M
Barilaro, MR
Garozzo, G
Sbaiz, L
Alberti, F
Camaschella, C
Citation: M. De Gobbi et al., TFR2 Y250X mutation in Italy, BR J HAEM, 114(1), 2001, pp. 243-244
Authors:
Iolascon, A
Delaunay, J
Wickramasinghe, SN
Perrotta, S
Gigante, M
Camaschella, C
Citation: A. Iolascon et al., Natural history of congenital dyserythropoietic anemia type II, BLOOD, 98(4), 2001, pp. 1258-1260
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:
Restagno, G
Gomez, AM
Sbaiz, L
De Gobbi, M
Roetto, A
Bertino, E
Fabris, C
Fiorucci, GC
Fortina, P
Camaschella, C
Citation: G. Restagno et al., A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan (TM)technology, GENET TEST, 4(2), 2000, pp. 177-181
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:
De Gobbi, M
Pasquero, P
Brunello, F
Paccotti, P
Mazza, U
Camaschella, C
Citation: M. De Gobbi et al., Juvenile hemochromatosis associated with beta-thalassemia treated by phlebotomy and recombinant human erythropoietin, HAEMATOLOG, 85(8), 2000, pp. 865-867
Authors:
Sivera, P
Bosio, S
Bertero, MT
Demaestri, M
Mazza, U
Camaschella, C
Citation: P. Sivera et al., G20210A homozygosity in antiphospholipid syndrome secondary to systemic lupus erythematosus, HAEMATOLOG, 85(1), 2000, pp. 109-110
Authors:
Piperno, A
Mariani, R
Arosio, C
Vergani, A
Bosio, S
Fargion, S
Sampietro, M
Girelli, D
Fraquelli, M
Conte, D
Fiorelli, G
Camaschella, C
Citation: A. Piperno et al., Haemochromatosis in patients with beta-thalassaemia trait, BR J HAEM, 111(3), 2000, pp. 908-914
Authors:
Camaschella, C
Zecchina, G
Lockitch, G
Roetto, A
Campanella, A
Arosio, P
Levi, S
Citation: C. Camaschella et al., A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins, BR J HAEM, 108(3), 2000, pp. 480-482
Authors:
Robson, KJH
Merryweather-Clark, AT
Pointon, JJ
Shearman, JD
Halsall, DJ
Kelly, A
Cox, TM
Rosenberg, WM
Howell, M
Eccles, D
Patch, C
Fowler, AV
Wallace, DF
Camaschella, C
Roetto, A
Zecchina, G
De Gobbi, M
Gasparini, P
Cadet, E
Vandwalle, JL
Capron, D
Rochette, J
Borot, N
Demangel, C
Dery, R
Vinel, JP
Pascal, JP
Coppin, H
Roth, MP
Citation: Kjh. Robson et al., Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience, BR J HAEM, 108(1), 2000, pp. 31-39
Authors:
Longo, F
Zecchina, G
Sbaiz, L
Fischer, R
Piga, A
Camaschella, C
Citation: F. Longo et al., The influence of hemochromatosis mutations on iron overload of thalassemiamajor, HAEMATOLOG, 84(9), 1999, pp. 799-803
Authors:
Cicilano, M
Zecchina, G
Roetto, A
Bosio, S
Infelise, V
Stefani, S
Mazza, U
Camaschella, C
Citation: M. Cicilano et al., Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome, HAEMATOLOG, 84(6), 1999, pp. 489-492
Authors:
Bosio, S
Zecchina, G
Cicilano, M
Roetto, A
Saito, AM
Camaschella, C
Citation: S. Bosio et al., Variation in the phenotypic expression of C282Y hemochromatosis in an Italian family, HAEMATOLOG, 84(2), 1999, pp. 184-185
Authors:
Camaschella, C
Fargion, S
Sampietro, M
Roetto, A
Bosio, S
Garozzo, G
Arosio, C
Piperno, A
Citation: C. Camaschella et al., Inherited HFE-unrelated hemochromatosis in Italian families, HEPATOLOGY, 29(5), 1999, pp. 1563-1564
Authors:
Alfarano, A
Circosta, P
Vallario, A
Camaschella, C
Indraccolo, S
Amadori, A
Caligaris-Cappio, F
Citation: A. Alfarano et al., Alternative splicing of CD79a (Ig alpha) and CD79b (Ig beta) transcripts in human B-CLL cells, CURR T MICR, 246, 1999, pp. 241-248
Authors:
Tolosano, E
Hirsch, E
Patrucco, E
Camaschella, C
Navone, R
Silengo, L
Altruda, F
Citation: E. Tolosano et al., Defective recovery and severe renal damage after acute hemolysis in hemopexin-deficient mice, BLOOD, 94(11), 1999, pp. 3906-3914
Authors:
Alfarano, A
Indraccolo, S
Circosta, P
Minuzzo, S
Vallario, A
Zamarchi, R
Fregonese, A
Calderazzo, F
Faldella, A
Aragno, M
Camaschella, C
Amadori, A
Caligaris-Cappio, F
Citation: A. Alfarano et al., An alternatively spliced form of CD79b gene may account for altered B-cellreceptor expression in B-chronic lymphocytic leukemia, BLOOD, 93(7), 1999, pp. 2327-2335
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
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1-22
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