Damien Luque Paz researcher
Luque Paz, Damien, 1986-....
VIAF ID: 238145541838896600388 (Personal)
Permalink: http://viaf.org/viaf/238145541838896600388
Preferred Forms
4xx's: Alternate Name Forms (1)
Works
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Absence of CALR mutation among a cohort of 394 unselected patients with a first episode of unprovoked venous thromboembolism |
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Circulating Cd34+ cell count differentiates primary myelofibrosis from other Philadelphia-negative myeloproliferative neoplasms: a pragmatic study. |
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Classification of urinary calculi in a pediatric population from Brittany |
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Concomitant CALR and LNK mutations leading to essential thrombocythemia with erythrocytosis |
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Detection of intrinsic pathway factor deficiency associated with bleeding risk by kaolin-based aPTT |
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Etude des mutations associées à l'aggravation dans les syndromes myéloprolifératifs |
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Expansion of a BCR-ABL clone in a JAK2 V617F myeloproliferative neoplasm treated by ruxolitinib. |
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Extinction of myeloproliferative neoplasm by acquisition of a lymphoid disease: JAK2 (V617F) and JAK2 exon 12 allele burden disappearance during the follow-up of two patients. |
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Genomic profiles and prognostic impact in myeloproliferative syndromes. |
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Imatinib Treatment of Chronic Myeloid Leukemia Reveals a Preexisting CALR-mutated Essential Thrombocythemia |
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Long-term follow-up of JAK2 exon 12 polycythemia vera: a French Intergroup of Myeloproliferative Neoplasms (FIM) study |
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A new point mutation in EPOR inducing a short deletion in congenital erythrocytosis. |
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Next generation sequencing redefines a triple negative essential thrombocythaemia as double-positive with rare mutations on JAK2 V617 and MPL W515 hotspots |
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Polymorphisme constitutionnel d’IFNL4 et réponse à l’interféron-α dans les SMP mutés JAK2 |
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Positive impact of molecular analysis on prognostic scores in essential thrombocythemia: a single center prospective cohort experience |
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Quantitative chimerism in CD3-negative mononuclear cells predicts prognosis in acute myeloid leukemia patients after hematopoietic stem cell transplantation |
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Sequential analysis of 18 genes in polycythemia vera essential thrombocythemia reveals an association between mutational status and clinical outcome. |
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Sequential mutational evaluation of CALR -mutated myeloproliferative neoplasms with thrombocytosis reveals an association between CALR allele burden evolution and disease progression |
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Targeted molecular characterization shows differences between primary and secondary myelofibrosis |
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WT1 gene is overexpressed in myeloproliferative neoplasms, especially in myelofibrosis |
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