European Clinical Laboratory, Molecular and Pathological (ECMP) criteria for prefibrotic JAK2V617F-Thrombocythemia and Polycythemia Vera versus MPL515- and CALR-Thrombocythemia and Myelofibrosis: From Dameshek to Michiels 1950-2018
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Heighten Science Publications Corporation
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https://www.bonemarrowjournal.com/articles/ijbmr-aid1002.pdf
Reference52 articles.
1. 1. Michiels JJ. Physiopathology, etiologic factors, diagnosis and course of polycythemia vera as related to therapy according to William Dameshek 1940-1950. Turkish J Hematol. 2013; 30: 102-110. Ref.: https://goo.gl/VWF3Td
2. 2. Michiels JJ, Ten Kate FWJ, Vuzevski VD, Abels J. Histopathology of erythromelalgia in thrombocythemia. Histopathology. 1984; 8: 669-678. Ref.: https://goo.gl/t79oZi
3. 3. Michiels JJ, Abels J, Steketee J, van Vliet HHDM, Vuzevski VD. Erythromelalgia caused by platelet mediated arteriolar inflammation and thrombosis in thrombocythemia. Ann Intern Med. 1985; 102: 466-471. Ref.: https://goo.gl/SctHNS
4. 4. Michiels JJ, Koudstaal PJJ, Mulder AH, Van Vliet HHDM. Transient neurologic and ocular manifestations in primary thrombocythemia. Neurology. 1993; 43: 1107-1110. Ref.: https://goo.gl/cYQy8p
5. 5. Michiels JJ, Juvonen E. Proposal for revised diagnostic criteria of essential thrombocythemia and polycythemia vera by the Thrombocythemia Vera Study Group (TVSG). Semin Thromb Hemostas. 1997; 23: 339-347. Ref.: https://goo.gl/9igXoi
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1. Bone marrow histology in CALR mutated thrombocythemia and myelofibrosis: results from two cross sectional studies in 70 newly diagnosed JAK2/MPL wild type thrombocythemia patients;International Journal of Bone Marrow Research;2019-06-21
2. Primary myelofibrosis is not primary anymore since the discovery of MPL515 and CALR mutations as driver causes of mono-linear megakaryocytic and dual megakaryocytic granulocytic myeloproliferation and secondary myelofibrosis;International Journal of Bone Marrow Research;2019-04-15
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