Results 31 to 40 of about 62,795 (319)

Platelets as mediators of Thromboinflammation in chronic Myeloproliferative Neoplasms [PDF]

open access: yes, 2019
Chronic myeloproliferative neoplasms (MPN) are stem cell disorders driven by mutations in JAK2, CALR, or MPL genes and characterized by myeloid proliferation and increased blood cell counts.
Heller, Paula Graciela   +1 more
core   +1 more source

POLYCYTHEMIA. [PDF]

open access: yesJAMA: The Journal of the American Medical Association, 1907
n ...
openaire   +2 more sources

Polycythemia vera and essential thrombocythemia: 2019 update on diagnosis, risk‐stratification and management

open access: yesAmerican journal of hematology/oncology, 2018
Disease Overview: Polycythemia vera (PV) and essential thrombocythemia (ET) are myeloproliferative neoplasms respectively characterized by erythrocytosis and thrombocytosis; other disease features include leukocytosis, splenomegaly, thrombosis, bleeding,
A. Tefferi, T. Barbui
semanticscholar   +1 more source

New Perspectives on Polycythemia Vera: From Diagnosis to Therapy

open access: yesInternational Journal of Molecular Sciences, 2020
Polycythemia vera (PV) is mainly characterized by elevated blood cell counts, thrombotic as well as hemorrhagic predisposition, a variety of symptoms, and cumulative risks of fibrotic progression and/or leukemic evolution over time.
A. Iurlo   +3 more
semanticscholar   +1 more source

High risk of long‐term neurodevelopmental impairment in donor twins with spontaneous twin anemia–polycythemia sequence

open access: yesUltrasound in Obstetrics and Gynecology, 2020
To evaluate the long‐term neurodevelopmental and behavioral outcomes in surviving infants of pregnancies with spontaneous twin anemia–polycythemia sequence (TAPS), to compare outcome between donors and recipients, and to investigate potential risk ...
L. Tollenaar   +9 more
semanticscholar   +1 more source

Diagnosis and genetic analysis of polycythemia in children and a novel EPAS1 gene mutationWhat is knownWhat is new?

open access: yesPediatrics and Neonatology, 2022
Background: Unlike in adults, there is no consensus on management and diagnosis of polycythemia in children. This study aims to evaluate the diagnosis and verify the algorithm in children with polycythemia.
Hatice Mine Cakmak   +3 more
doaj  

Polycythemia causing posterior segment vascular occlusions

open access: yesOman Journal of Ophthalmology, 2017
A 44-year-old male patient presented with features suggestive of transient central retinal artery occlusion (CRAO) followed by permanent CRAO and lateral posterior ciliary artery occlusion. He had diagnostic features of polycythemia vera (PV).
Suganeswari Ganesan   +2 more
doaj   +1 more source

Splenomegaly impacts prognosis in essential thrombocythemia and polycythemia vera: A single center study [PDF]

open access: yes, 2019
Splenomegaly is one of the major clinical manifestations of primary myelofibrosis and is common also in other chronic Philadelphia-negative myeloproliferative neoplasms, causing symptoms and signs and affecting quality of life of patients diagnosed with ...
Accurso V.   +8 more
core   +1 more source

Ruxolitinib versus standard therapy for the treatment of polycythemia vera.

open access: yesNew England Journal of Medicine, 2015
BACKGROUND Ruxolitinib, a Janus kinase (JAK) 1 and 2 inhibitor, was shown to have a clinical benefit in patients with polycythemia vera in a phase 2 study.
A. Vannucchi   +16 more
semanticscholar   +1 more source

Givinostat: an emerging treatment for polycythemia vera

open access: yesExpert Opinion on Investigational Drugs, 2020
Introduction Polycythemia vera (PV), a Philadelphia chromosome-negative myeloproliferative neoplasm, is characterized by panmyelosis, pancytosis, and a JAK2 mutation.
H. Chifotides, P. Bose, S. Verstovsek
semanticscholar   +1 more source

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