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Lucio Luzzatto

Formats
  1. Journal Article (59)
  2. Meeting Abstract (44)
  3. Book Section (2)
Groups
  1. Department of Medicine (28)
  2. Hematologic Malignancies, Division of (24)
  3. Department of Pathology and Laboratory Medicine (23)
  4. Center for Hematologic Malignancies (22)
  5. GSK Faculty (18)
  6. Sloan Kettering Institute Faculty (15)

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People
  1. Monica Bessler (27)
  2. Khedoudja Nafa (23)
  3. Rosario Notaro (22)
  4. David Araten (19)
  5. Vittorio Rosti (14)
  6. Anastasios Karadimitris (13)

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Years
  1. 2020 (1)
  2. 2012 (1)
  3. 2011 (1)
  4. 2009 (1)
  5. 2005 (2)
  6. 2004 (1)

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Publications
  1. Blood (40)
  2. British Journal of Haematology (11)
  3. American Journal of Human Genetics (6)
  4. Cancer Research (3)
  5. Proceedings of the National Academy of Sciences of the United States of America (3)
  6. EMBO Journal (2)

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Publishers
  1. American Society of Hematology (40)
  2. John Wiley & Sons (12)
  3. Cell Press (8)
  4. American Association for Cancer Research (5)
  5. Nature Publishing Group (5)
  6. Elsevier Science, Inc. (3)

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Results (105)

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  • Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia
    Journal Article

    Vulliamy, T. J.; Kaeda, J. S.; Ait-Chafa, D.; Mangerini, R.; Roper, D.; Barbot, J.; Mehta, A. B.; Athanassiou-Metaxa, M.; Luzzatto, L.; Mason, P. J.
    British Journal of Haematology (1998)

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  • New somatic mutation in the PIG-A gene emerges at relapse of paroxysmal nocturnal hemoglobinuria
    Journal Article

    Nafa, K.; Bessler, M.; Deeg, H. J.; Luzzatto, L.
    Blood (1998)

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  • The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplications
    Journal Article

    Nafa, K.; Bessler, M.; Castro-Malaspina, H.; Jhanwar, S.; Luzzatto, L.
    Blood Cells, Molecules, and Diseases (1998)

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  • Search for genetic factors thrombosis in paroxysmal nocturnal hemoglobinuria: The possible role of a mutant methylenetetrahydrofolate reductase (C677T)
    Meeting Abstract

    Nafa, K.; Bessler, M.; Castro-Malaspina, H.; Luzzatto, L.
    Blood (1997)

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  • Chromosomal abnormalities in paroxysmal nocturnal hemoglobinuria (PNH)
    Meeting Abstract

    Araten, D.; Bessler, M.; Nafa, K.; Longo, L.; Karadimitris, A.; Freeman, J.; Anastagnopoulous, N.; Beris, P.; Boulad, F.; Castro-Malaspina, H.; more...
    Blood (1997)

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  • Mice heterozygous for complete glucose 6-phosphate dehydrogenase (G6PD) deficiency are viable and show somatic cell selection
    Meeting Abstract

    Longo, L.; Rosti, V.; Gaboli, M.; Tabarini, D.; Pandolfi, P. P.; Luzzatto, L.
    Blood (1997)

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  • PNH-like lymphocytes are competent for generating the entire immune system in rag null mice
    Meeting Abstract

    Rosti, V.; Drappa, J.; Tremml, G.; Cattoretti, G.; Elkon, K. B.; Luzzatto, L.; Bessler, M.
    Blood (1997)

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  • Survey of mutations of the PIG-A gene in Paroxysmal Nocturnal Hemoglobinuria: Phenotype-genotype correlations
    Meeting Abstract

    Nafa, K.; Bessler, M.; Luzzatto, L.
    Blood (1997)

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  • Retroviral mediated transfer and expression of the human glucose 6-phosphate dehydrogenase (G6PD) gene in mouse bone marrow cells
    Meeting Abstract

    Rovira, A.; Gallardo, H.; De Angioletti, M.; Murphy, C.; Rosti, V.; Liu, D.; Sadelain, M.; Luzzatto, L.
    Blood (1997)

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  • Mutations of the PIG-A gene in paroxysmal nocturnal hemoglobinuria (PNH): An update survey
    Meeting Abstract

    Nafa, K.; Bessler, M.; Luzzatto, L.
    American Journal of Human Genetics (1997)

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