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Leukemia & Lymphoma|September 1, 1994
Dyskeratosis congenita is a chromosomal instability disorderI Dokal, L LuzzattoThe Journal of Clinical Investigation|December 1, 1992
Anomalous rearrangements of the immunoglobulin heavy chain genes in human leukemias support the loop-out mechanism of class switchM Laffan, L LuzzattoLeukemia|August 2, 2001
The cellular pathogenesis of paroxysmal nocturnal haemoglobinuriaA Karadimitris, L LuzzattoRetina (Philadelphia, Pa.)|August 10, 2004
Verteporfin therapy in age-related macular degeneration (VAM): an open-label multicenter photodynamic therapy study of 4,435 patientsNeil M Bessler, British Journal of Haematology|January 1, 1992
Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instabilityS Filosa, V Calabrò, D Vallone, et al.Molecular and Biochemical Parasitology|June 1, 1990
Expression and characterization of glucose-6-phosphate dehydrogenase of Plasmodium falciparumB Kurdi-Haidar, L LuzzattoNature|February 6, 1985
Adaptation of Plasmodium falciparum to glucose 6-phosphate dehydrogenase-deficient host red cells by production of parasite-encoded enzymeE A Usanga, L LuzzattoEuropean Journal of Immunology|February 1, 1993
V kappa gene segments rearranged in chronic lymphocytic leukemia are distributed over a large portion of the V kappa locus and do not show somatic mutationS D Wagner, L LuzzattoEuropean Journal of Haematology|September 1, 1991
Fc III receptors (FcRIII) on granulocytes: a specific and sensitive diagnostic test for paroxysmal nocturnal hemoglobinuria (PNH)M Bessler, J FehrPageof 162