Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Platelet Abnormality"'
Publikováno v:
Redox Biology, Vol 57, Iss , Pp 102507- (2022)
Type 2 diabetes mellitus (T2DM) is a strong indicator of late stent thrombosis (LST). Platelet bioenergetic dysfunction, although critical to the pathogenesis of diabetic macrovascular complications, remains uncharacterized in T2DM patients who devel
Externí odkaz:
https://doaj.org/article/8124a245a5304691b12ee9fcc2028f4d
Publikováno v:
Journal of Pharmaceutical Research International. :81-85
Thrombocytopenia is defined as platelet count < 1.5 lakhs/cumm. It is the commonest platelet abnormality observed in clinical practice with different clinical expression. Thrombocytopenias in hematological malignancies are clonal proliferations of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff38c2d437cdc70f5ff627de791296dc
https://doi.org/10.9734/jpri/2020/v32i1230564
https://doi.org/10.9734/jpri/2020/v32i1230564
Akademický článek
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Autor:
Taisuke Kanaji
Publikováno v:
Japanese Journal of Thrombosis and Hemostasis. 28:55-58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83f53035c81fe007071bdc0bd8c53c79
https://doi.org/10.2491/jjsth.28.55
https://doi.org/10.2491/jjsth.28.55
Publikováno v:
Journal of Natural Science, Biology, and Medicine
Journal of Natural Science, Biology and Medicine
Journal of Natural Science, Biology and Medicine
One of the major health hazards which is prevalent and dangerous is the dengue fever which causes the death of many people. This may be associated with a variety of mucocutaneous manifestations which may be of help in early diagnosis. Many biochemica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ba27cffee298378c621a5e9f60cf95c
http://europepmc.org/articles/PMC3633297
http://europepmc.org/articles/PMC3633297
Autor:
Alvin H. Schmaier
Publikováno v:
Concise Guide to Hematology
This chapter aims to provide a simple diagnostic framework in which the physician can approach most patients with abnormal bleeding in a logical fashion to recognize the underlying cause. The diagnostic approach to bleeding disorders is based upon a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c3054033829436601f1c7099b08f5ac
https://doi.org/10.1002/9781444345254.ch10
https://doi.org/10.1002/9781444345254.ch10
Physical and Biochemical Characteristics of Platelets in Severely Malnourished Children with Purpura
Publikováno v:
Scandinavian Journal of Haematology. 8:321-327
Platelets from a group of 24 malnourished children with purpura, and a group of 28 clinically healthy adults and 5 normal children, were studied with determination of platelet mean diameter, soluble protein, lactate concentration and platelet viscous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc4be523ac8975a71108dc1453677d12
https://doi.org/10.1111/j.1600-0609.1971.tb00881.x
https://doi.org/10.1111/j.1600-0609.1971.tb00881.x
Autor:
Steve P. Watson, Marie Lordkipanidzé, Gillian C. Lowe, Stan Heptinstall, Ban B. Dawood, Susan C. Fox, Natalia Dovlatova, Jane May
Mild platelet function disorders (PFDs) are complex and difficult to diagnose. The current gold standard test, light transmission aggregometry (LTA), including lumi-aggregometry, is time and labour intensive and blood samples must be processed within
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f288118793a9a109f49b1439c7b15cb
https://europepmc.org/articles/PMC4405765/
https://europepmc.org/articles/PMC4405765/
Publikováno v:
Platelets. 3(3)
The enzyme acid phosphatase (ACP) exists as a number of isoenzymes in serum. This fact hinders its use as a tumour marker of prostatic carcinoma as other tissues can contribute to serum ACP levels. The prostate isoenzymes have been designated 2 and 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca0d15ea264008a18bc28d4e43743a59
https://pubmed.ncbi.nlm.nih.gov/21043910
https://pubmed.ncbi.nlm.nih.gov/21043910
Autor:
Frenny Sheth, Joris Andrieux, Darshana Nayak, Mahbubur Rahman, Jayesh Sheth, Anand Pandit, Chaitanya Datar
Publikováno v:
Clinical Medicine Insights. Pediatrics
Clinical Medicine Insights: Pediatrics, Vol 8 (2014)
Clinical Medicine Insights: Pediatrics, Vol 8 (2014)
Terminal 11q deletion, known as Jacobsen syndrome (JBS), is a rare genetic disorder associated with numerous dysmorphic features. We studied two cases with multiple congenital anomalies that were cytogenetically detected with deletions on 11q encompa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::462953ea71c9e68649ef308f945e3e04
https://doi.org/10.4137/cmped.s18121
https://doi.org/10.4137/cmped.s18121