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Citation: S. Defranco et al., Defective function of Fas in patients with type 1 diabetes associated withother autoimmune diseases, DIABETES, 50(3), 2001, pp. 483-488
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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:
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Citation: U. Ramenghi et al., Diamond-Blackfan anemia: Report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population, BL CELL M D, 26(5), 2000, pp. 417-422
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Citation: C. Pignata et al., Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children, CLIN EXP IM, 121(1), 2000, pp. 53-58
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Citation: C. Zeidler et al., Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation, BLOOD, 95(4), 2000, pp. 1195-1198
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Citation: U. Ramenghi et al., Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer, BLOOD, 95(10), 2000, pp. 3176-3182
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Citation: F. Bottarel et al., The cell death-inducing ability of glycoprotein 120 from different HIV strains correlates with their ability to induce CD4 lateral association with CD95 on CD4(+) T cells, AIDS RES H, 15(14), 1999, pp. 1255-1263
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Citation: Ma. Santucci et al., Long-term bone marrow cultures in Diamond-Blackfan anemia reveal a defect of both granulomacrophage and erythroid progenitors, EXP HEMATOL, 27(1), 1999, pp. 9-18
Authors:
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Garelli, E
Valtolina, S
Campagnoli, MF
Timeus, F
Crescenzio, N
Mair, M
Varotto, S
D'Avanzo, M
Nobili, B
Massolo, F
Mori, PG
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Gustavsson, P
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Dianzani, I
Citation: U. Ramenghi et al., Diamond-Blackfan anaemia in the Italian population, BR J HAEM, 104(4), 1999, pp. 841-848
Authors:
Willig, TN
Draptchinskaia, N
Dianzani, I
Ball, S
Niemeyer, C
Ramenghi, U
Orfali, K
Gustavsson, P
Garelli, E
Brusco, A
Tiemann, C
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Bouchier, C
Cicchiello, L
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Citation: Tn. Willig et al., Mutations in ribosomal protein S19 gene and Diamond Blackfan anemia: Wide variations in phenotypic expression, BLOOD, 94(12), 1999, pp. 4294-4306