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HAEMATOLOGICA
Rivista
Codice:
E215747
ISSN:
1592-8721
Dati Generali
Dati Generali
Pubblicazioni (29)
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Ordina Pubblicazioni:
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A MONOALLELIC LOSS-FUNCTION MUTATION IN THE THROMBOPOIETIN (THPO) GENE IS RESPONSIBLE FOR A NEW FORM OF INHERITED THROMBOCYTOPENIA (IT)
Articolo
A targeted gene signature stratifying mediastinal gray zone lymphoma into classical HL-like or PMBL-like subtypes
Articolo
Acquired von Willebrand syndrome and monoclonal gammopathy: clinical characterization and recovery to infusion of VWF-containing concentrates
Articolo
CAR T expansion and systemic inflammation: diverging impacts on large B-cell lymphoma therapy in the multicenter CART SIE study
Articolo
Characterization, outcome and identification of prognostic factors for patients with systemic immunoglobulin light-chain amyloidosis requiring dialysis prior to initial anti-clonal therapy
Articolo
Chemotherapy-induced leukonychia
Articolo
Clonal megakaryocyte dysplasia with normal blood values: a covert, thrombosis-prone, early myeloproliferative neoplasm
Articolo
Constant activation of the RAF-MEK-ERK pathway as a diagnostic and therapeutic target in hairy cell leukemia
Articolo
Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation
Articolo
ETV6-related thrombocytopenia: dominant negative effect of mutations as common pathogenic mechanism
Articolo
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup
Articolo
GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme
Articolo
Genome sequencing in the management of myelodysplastic syndromes and related disorders
Articolo
Halting the Vicious Cycle Within the Multiple Myeloma Ecosystem: Blocking JAM-A on Bone Marrow Endothelial Cells Restores the Angiogenic Homeostasis and Suppresses Tumor Progression
Articolo
Infections in lower-risk myelodysplastic syndromes - prevalence and risk factors: a report from the European MDS Registry
Articolo
KMT2D mutations and TP53 disruptions are poor prognostic biomarkers in mantle cell lymphoma receiving high-dose therapy: a FIL study
Articolo
Lenalidomide-based triplet regimens in first relapsed multiple myeloma patients: real-world evidence from a propensity score matched analysis
Articolo
NOVEL PERSPECTIVES IN GENOTYPE-PHENOTYPE CORRELATIONS IN MYH9-RELATED DISEASE: NO LONGER JUST A MATTER OF HEAD OR TAIL
Articolo
NOVEL RUNX1 MUTATIONS IN FAMILIES WITH INHERITED THROMBOCYTOPENIA
Articolo
Nodular lesions of the liver in multiple myeloma
Articolo
Oral melphalan and dexamethasone grants extended survival with minimal toxicity in AL amyloidosis: long-term results of a risk-adapted approach
Articolo
PAS positive monocytes in Whipple s disease.
Articolo
Prognosis in marginal zone lymphoma: a comprehensive review
Articolo
Reduced intensity stem cell transplantation for advanced soft tissue sarcomas in adults: a retrospective analysis of the European Group for Blood and Marrow Transplantation
Articolo
TENT5C/FAM46C modulation in vivo reveals a trade-off between antibody secretion and tumor growth in multiple myeloma
Articolo
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy
Articolo
Treating advanced cardiac damage in light chain amyloidosis: still an unmet need
Articolo
Update on treatment of light chain amyloidosis
Articolo
VEGF-induced Ca2+signals are deranged in endothelial progenitor cells from patients with myelofibrosis carrying JAK2 mutations
Abstract
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