Revised international prognostic scoring system for myelodysplastic syndromes.
By P. Greenberg, H. Tuechler, J. Schanz, G. Sanz, G. Garcia-Manero, F. Solé, J. Bennett, D. Bowen, P. Fenaux, F. Dreyfus and 24 more. Blood, 2012
2,977 citations recorded by the source corpus.
Subfields: Emergency Medicine, Genetics, Hematology
View Paper: https://www.semanticscholar.org/paper/f662db5fa469214962217bd28946d69ad5ab0861
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Citations in the corpus
- Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. (2017, positive): “Bone marrow failure is the usual cause of death in both AML and MDS-EB2, and most of the latter die without “progression to AML,” with data suggesting the natural history of MDS-EB2 is more similar to AML than to lower risk MDS.(128,129) These observations suggest that it is best to determine eligib”
- The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms (2022, methodology): “Cutaneous mastocytosis Urticaria pigmentosa/Maculopapular cutaneous mastocytosis Monomorphic Polymorphic Diffuse cutaneous mastocytosis Cutaneous mastocytoma Isolated mastocytoma Multilocalized mastocytoma Systemic mastocytosis Bone marrow mastocytosis Indolent systemic mastocytosis Smoldering syste”
- The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. (2016, positive): “The myeloblast percentage, as determined by counting wellprepared, cellular BM aspirate smears and/or touch preparations and a PB smear, remains critical in defining theWHOMDScategories and as risk strata in the Revised International Prognostic Scoring System (IPSS-R).(54) The presence of 1%blasts i”
- GENeration (2015, background): “Once the "front-end" concept was working, the remaining conversion effort, to get all of NASTRAN on a "4G" computer, while involving significant volumes of code, would not require the further system type extensions.”