Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Hemorrhagic thrombocythemia"'
Publikováno v:
Journal of Hematology & Thromboembolic Diseases.
A 9-year-old Caucasian boy presented in 1994 with severe headache, attacks of migraine, aggressive behavior and minor bleeding symptoms. Initial abnormal laboratory data were a platelet count of 1596 × 109/L and slight splenomegaly on echogram. Low-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0821583969dc3b68022051486a9be67
https://doi.org/10.4172/2329-8790.1000274
https://doi.org/10.4172/2329-8790.1000274
Autor:
Claire N. Harrison, Steven Okoli
Publikováno v:
Journal of blood medicine
In 1934, Epstein and Goedel used the term hemorrhagic thrombocythemia to describe a disorder characterized by permanent elevation of a platelet count to more than three times normal, hyperplasia of megakaryocytes, and the tendency for venous thrombos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac68b540700ad710dd259b651d29b36f
http://europepmc.org/articles/PMC3262348
http://europepmc.org/articles/PMC3262348
Autor:
Unto Uotila
Publikováno v:
Acta Medica Scandinavica. 95:136-150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5c9d213a7ce479f65f8874e85e8ae11
https://doi.org/10.1111/j.0954-6820.1938.tb17110.x
https://doi.org/10.1111/j.0954-6820.1938.tb17110.x
Autor:
Jan Jacques Michiels
Publikováno v:
Journal of Hematology & Thromboembolic Diseases.
We analysed between 1908 and 1985 of two hundred cases of thrombocythemia from the literature between 1908 and 1985. Erythromelalgic, acrocyanotic ischemia and digital gangrene, cerebral or coronary ischemic events (erythromelalgic thrombotic thrombo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dc7494dc6b0a765266930b649fd10b9
https://doi.org/10.4172/2329-8790.1000169
https://doi.org/10.4172/2329-8790.1000169
Autor:
Jan Jacques Michiels
Publikováno v:
Journal of Hematology & Thromboembolic Diseases.
Aspirin responsive erythromelalgia is the presenting symptom of thrombocythemia in patients with essential thrombocythemia (ET) and polycythemia vera (PV). Skin punch biopsies taken from the affected areas of erythromelalgia and acrocyanotic compicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8be28b29540216ff092d9754931a766f
https://doi.org/10.4172/2329-8790.1000149
https://doi.org/10.4172/2329-8790.1000149
Autor:
Scott Murphy
Publikováno v:
Thrombosis and Haemostasis. 78:622-626
With these uncertainties, which patients with ET and PV should receive myelosuppressive therapy and accept its possible risks? Remembering the generalization from the literature that most patients with ET who are to have a catastrophic thrombosis eit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7812fd74f0c8e6769a741284f04502
https://doi.org/10.1055/s-0038-1657600
https://doi.org/10.1055/s-0038-1657600
Publikováno v:
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 23(5)
Essential thrombocythemia (ET) is a risk factor for ischemic stroke and, far more rarely, hemorrhage. We report the case of an untreated 32-year-old woman with a history of JAK2 V617F–positive ET with cerebellar and subarachnoid hemorrhages without
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4fc89fe64a9a2907005f947157a8314
https://pubmed.ncbi.nlm.nih.gov/24582788
https://pubmed.ncbi.nlm.nih.gov/24582788
Autor:
Jan Jacques Michiels
Publikováno v:
Leukemia & Lymphoma. 22:1-14
According to strict morphological, biochemical and cytogenetic criteria Philadelphia chromosome positive essential thrombocythemia and chronic granulocytic leukemia constitute a separate malignant and individual disease entity, whereas Philadelphia c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50be8ac50553d990e039745bb9e6716d
https://doi.org/10.3109/10428199609074356
https://doi.org/10.3109/10428199609074356
Autor:
Christine S. Hunter, Gregory G. Marino, Michael Anderson, George A. Luiken, Frederick E. Millard, Martin J. Edelman, Michael P. Kosty
Publikováno v:
American Journal of Hematology. 33:27-31
Essential thrombocythemia (ET) is a myeloproliferative disorder characterized by isolated overproduction of platelets, thrombohemorrhagic complications, and a median age of 50-60. When it occurs in younger patients, the incidence of complications has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb568bd92b8014dd8a0b5b7424e6dc04
https://doi.org/10.1002/ajh.2830330106
https://doi.org/10.1002/ajh.2830330106
Autor:
J. J. Michiels
Publikováno v:
27. Hämophilie-Symposion Hamburg 1996 ISBN: 9783540629153
Essential thrombocythemia and thrombocythemia in polycythemia vera manifest itself in two clinical pictures: thrombotic thrombocythemia and hemorrhagic thrombocythemia. The broad spectrum of microcirculatory events including erythromelalgia and neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6a3863ff2bfa487e2a7815c1fba68d3
https://doi.org/10.1007/978-3-642-80403-8_63
https://doi.org/10.1007/978-3-642-80403-8_63
