Myeloproliferative neoplasms in Budd-Chiari syndrome and portal vein thrombosis: a meta-analysis

JH Smalberg, LR Arends, DC Valla… - Blood, The Journal …, 2012 - ashpublications.org
Myeloproliferative neoplasms (MPNs) are the most common cause of Budd-Chiari syndrome
(BCS) and nonmalignant, noncirrhotic portal vein thrombosis (PVT). In this meta-analysis …

Polycythemia vera and essential thrombocythemia: 2012 update on diagnosis, risk stratification, and management

A Tefferi - American journal of hematology, 2012 - Wiley Online Library
Disease overview: Polycythemia vera (PV) and essential thrombocythemia (ET) are
myeloproliferative neoplasms primarily characterized by erythrocytosis and thrombocytosis …

One thousand patients with primary myelofibrosis: the mayo clinic experience

A Tefferi, TL Lasho, T Jimma, CM Finke, N Gangat… - Mayo Clinic …, 2012 - Elsevier
Objective To share our decades of experience with primary myelofibrosis and underscore
the importance of outcomes research studies in designing clinical trials and interpreting their …

SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value

MM Patnaik, TL Lasho, JM Hodnefield… - Blood, The Journal …, 2012 - ashpublications.org
SF3B1 mutations were recently reported in myelodysplastic syndromes (MDSs), especially
in the presence of ring sideroblasts (RSs). We sought to define the interaction between …

SRSF2 mutations in primary myelofibrosis: significant clustering with IDH mutations and independent association with inferior overall and leukemia-free survival

TL Lasho, T Jimma, CM Finke, M Patnaik… - Blood, The Journal …, 2012 - ashpublications.org
Among spliceosome component mutations, those involving SF3B1 are most frequent in
myelodysplastic syndromes with ring sideroblasts (MDS-RS;∼ 75% incidence) and SRSF2 …

Myeloid malignancies: mutations, models and management

A Murati, M Brecqueville, R Devillier, MJ Mozziconacci… - BMC cancer, 2012 - Springer
Myeloid malignant diseases comprise chronic (including myelodysplastic syndromes,
myeloproliferative neoplasms and chronic myelomonocytic leukemia) and acute (acute …

IDH mutations in primary myelofibrosis predict leukemic transformation and shortened survival: clinical evidence for leukemogenic collaboration with JAK2V617F

A Tefferi, T Jimma, NH Sulai, TL Lasho, CM Finke… - Leukemia, 2012 - nature.com
Isocitrate dehydrogenase (IDH) mutations are frequent in blast-phase myeloproliferative
neoplasms and might therefore contribute to leukemic transformation. We examined this …

Differential prognostic effect of IDH1 versus IDH2 mutations in myelodysplastic syndromes: a Mayo Clinic study of 277 patients

MM Patnaik, CA Hanson, JM Hodnefield, TL Lasho… - Leukemia, 2012 - nature.com
Unlike the case with acute myeloid leukemia, there is limited information on the prognostic
impact of isocitrate dehydrogenase (IDH) mutations in myelodysplastic syndromes (MDS). In …

Imputation of exome sequence variants into population-based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing …

PL Auer, JM Johnsen, AD Johnson, BA Logsdon… - The American Journal of …, 2012 - cell.com
Researchers have successfully applied exome sequencing to discover causal variants in
selected individuals with familial, highly penetrant disorders. We demonstrate the utility of …

Guideline for the diagnosis and management of myelofibrosis

JT Reilly, MF McMullin, PA Beer, N Butt… - British journal of …, 2012 - Wiley Online Library
The guideline group regarding the diagnosis and management of myelofibrosis was
selected to be representative of UK‐based medical experts, together with a contribution from …