Zobrazeno 1 - 10
of 167
pro vyhledávání: '"JAK-2"'
Autor:
Annadora Morena, Domenico Cirillo, Raffaele Natale, Clelia Nasti, Tullia Torella, Rossella Di Domenico, Fabrizio Pasanisi, Lidia Santarpia
Publikováno v:
Italian Journal of Medicine, Vol 18, Iss 3 (2024)
A 71-year-old woman was admitted to the hospital after consuming food due to acute malnutrition and abdominal pain. Reduced patency of all jejunoileal branches and the superior mesenteric artery was observed in the abdominal computed tomography scan.
Externí odkaz:
https://doaj.org/article/dc1ca86bef71491d81dc223526e386e7
Publikováno v:
Sri Lanka Journal of Medicine, Vol 30, Iss 2, Pp 129-132 (2021)
Background: Cerebral venous sinus thrombosis (CVST) has been reported to present with intracranial haemorrhage (ICH) due to its varying effects on cerebral circulation. Polycythaemia rubra vera (PRV) is one of the rare causes of CVST. Case Report:
Externí odkaz:
https://doaj.org/article/eec4272a43a14e0fbcf8d3547a9bfbcf
Autor:
David Orion, Ze'ev Itsekson-Hayosh, Shlomi Peretz, Rom Mendel, Gal Yaniv, Moshe Attia, Drorit Grizim-Merkel
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundCerebral sinus venous thrombosis (CSVT) is a rare neurovascular entity, usually associated with acquired or genetic hypercoagulable states. In up to 30% of the cases it remains idiopathic. Bone marrow proliferation disorders that are associ
Externí odkaz:
https://doaj.org/article/7c08ed4677744de09d0f803b88293de4
Publikováno v:
Liječnički vjesnik, Vol 145, Iss Supp 2, Pp 90-90 (2023)
Externí odkaz:
https://doaj.org/article/ef339e614ba84911b8f44b2999050d7b
Akademický článek
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Publikováno v:
Acta Biomedica Scientifica, Vol 2, Iss 4, Pp 39-42 (2017)
Ph-negative myeloproliferative neoplasm are the group of hematologic disorders which includes primary myelofibrosis, polycythemia vera, essential trombocytemia and several rare diseases. After the discovery of V617 Fgain-of-function mutation the new
Externí odkaz:
https://doaj.org/article/a4815a4296a44801ba5a931e35d897bd
Autor:
Thea Kristin Våtsveen, Anne-Marit Sponaas, Erming Tian, Qing Zhang, Kristine Misund, Anders Sundan, Magne Børset, Anders Waage, Gaute Brede
Publikováno v:
Journal of Hematology & Oncology, Vol 9, Iss 1, Pp 1-9 (2016)
Abstract Background Multiple myeloma is an incurable complex disease characterized by clonal proliferation of malignant plasma cells in a hypoxic bone marrow environment. Hypoxia-dependent erythropoietin (EPO)-receptor (EPOR) signaling is central in
Externí odkaz:
https://doaj.org/article/c1d37908ecac46e5a181d4fb359c5a20
Publikováno v:
Liječnički vjesnik
Volume 145
Issue Supp 2
Volume 145
Issue Supp 2
Publikováno v:
Turkish Journal of Hematology, Vol 30, Iss 1, Pp 8-12 (2013)
OBJECTIVE: The MPL gene encodes the thrombopoietin receptor. Recently MPL mutations (MPL W515L or MPL W515K) were described in patients with essential thrombocythemia (ET) and primary (idiopathic) myelofibrosis (PMF). The prevalence and the clinical
Externí odkaz:
https://doaj.org/article/158ca4292e6b46ada24547765caf25dd
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 8, Iss 0, Pp e2016050-e2016050 (2016)
This is the report of the clinical case of a patient who presents the association of a JAK-2 positive chronic myeloproliferative neoplasia to a subsequent 5q- myelodysplastic syndrome, developed after about 14 years from the first diagnosis. Patient
Externí odkaz:
https://doaj.org/article/a32bf44538ca4fac89b05b81058a8889