193 research outputs found
JAK2V617F, CALR, and MPL Mutations and Bone Marrow Histology in Patients with Essential Thrombocythaemia
p53 protein expression in patients with myelodysplasia treated with allogeneic bone marrow transplantation
WHO Clinical Molecular and Pathological (WHO-CMP) Features of Congenital MPLS505N and the Acquired MPL W515l/K Mutated Essential Thrombocythemia and Myelofibrosis
Autosomal Dominant Hereditary Essential Thrombocythemia due to a Gain of Function Mutation in the Thrombopoietin (TPO) and JAK2 Gene as the Cause of Congenital Aspirin-Responsive Sticky Platelet Syndrome: Personal Experiences and Review of the Literature
Prognostic value of the rapidity of bone marrow blast cell proliferation in adult acute lymphoblastic leukemia
Prognostic value of quantitative analysis of WT1 gene transcripts in adult acute lymphoblastic leukemia
Myelodysplastic syndrome with del (5q) and JAK2V617F mutation transformed to acute myeloid leukaemia with complex karyotype
Intrasinusoidal bone marrow infiltration and splenic marginal zone lymphoma: a quantitative study
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