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Lymphoproliferative disorders after organ transplantation: a report of 24 cases observed in a single center.
PURPOSE Organ recipients are at a high risk of post-transplant lymphoproliferative disorders (PTLDs) as a complication of immunosuppressive therapy. We report the incidence, clinical presentation,Expand
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Patterns of Epstein-Barr virus latent and replicative gene expression in Epstein-Barr virus B cell lymphoproliferative disorders after organ transplantation.
B cell lymphoproliferative disorders arising in organ transplant recipients (B cell posttransplant lymphoproliferative disorders [PTLD]) are generally associated with EBV. In previous reports, B cellExpand
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Chronic Lymphocytic Leukemia Associated with Myelodysplastic Syndrome and/or Chronic Myeloid Leukemia: Evidence for Independent Clonal Chromosomal Evolution
We describe the cytogenetic findings of three cases with simultaneous or sequential development of a B-chronic lymphocytic leukemia (B-CLL) and either a myelodysplastic syndrome (MDS) in 2 cases or aExpand
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Automated detection of malaria by means of the haematology analyser Coulter GEN.S.
The haematology analysers Coulter(R) GEN.S(TM) and LH(TM) give a set of data--'positional parameters'--which define each WBC population by mean of index values, the mean and the standard deviationExpand
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Recombination pattern of the TCR γ locus in human peripheral T‐cell lymphomas
The recombination events of the γ and β T‐cell receptor (TCR) loci were analysed in a series of 39 peripheral T‐cell lymphomas (PTCLs) in association with the expression of TCR chains. In TCR αβExpand
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Lymphocyte volume and conductivity indices of the haematology analyser Coulter GEN.S in lymphoproliferative disorders and viral diseases.
The haematology analyser Coulter GEN.S gives a set of data -'positional parameters'- defining white blood cell (WBC) populations by mean of index values (mean and standard deviation of volume,Expand
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The 17p-syndrome: a distinct myelodysplastic syndrome entity?
The 17p- syndrome is a subset of myelodysplastic syndrome characterized by "typical" dysgranulopoïesis, combining a pseudo-Pelger-Hüet and a deletion of the short arm of chromosome 17. We describeExpand
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An unusual case of hemochromatosis due to a new compound heterozygosity in HFE (p.[Gly43Asp;His63Asp]+[Cys282Tyr]): structural implications with respect to binding with transferrin receptor 1
Most adults affected with HFE hereditary hemochromatosis (HH type 1, MIM♯ 235200) are homozygous for the p.Cys282Tyr mutation in HFE (NC_000006.10, region 26195427 to 26205038). The aim of this studyExpand
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CD3+ CD8+ CD56− clonal large granular lymphocyte leukaemia and HIV infection
High‐grade malignant lymphomas associated with HIV infection are usually derived from B lymphocytes. Although a broad spectrum of T‐cell‐derived malignancies has been described, no case of monoclonalExpand
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