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pro vyhledávání: '"Familial hyperlipoproteinemia"'
Akademický článek
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Publikováno v:
Medical Laboratory Journal, Vol 6, Iss 1, Pp 73-84 (2012)
Abstract Background and objectives: Familial hypercholesterolemia (FH) is an autosomal disorder characterized by increased levels of total cholesterol and low density lipoprotein cholesterol. The FH clinical phenotype has been associated with increas
Externí odkaz:
https://doaj.org/article/eb2eb51328cc452e80619738077d036b
Publikováno v:
World Journal of Gastroenterology
Hypertriglyceridemic pancreatitis (HTGP) accounts for up to 10% of acute pancreatitis presentations in non-pregnant individuals and is the third most common cause of acute pancreatitis after alcohol and gallstones. There are a number of retrospective
Autor:
Stanislav Filip, M. Kostal, M. Kubisova, Jaroslav Maly, Vladimír Bláha, I. Foralova, Miriam Lánská, Milan Bláha
Publikováno v:
Atherosclerosis Supplements. 14:77-81
Objective Mean platelet volume is arousing increasing interest as a new independent cardiovascular risk factor. Large platelets are likely to be more reactive. If mean platelet volume would drop after LDL-lowering therapy, decreased MPV could be one
Autor:
Gianpaolo Russi
Publikováno v:
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis. 53(3)
During pregnancy physiological changes occur in the lipid metabolism due to changing hormonal conditions: the LDL cholesterol (LDL-C), triglycerides (TG) and lipoprotein(a) [Lp(a)] increase throughout pregnancy. Common lipoprotein disorders are assoc
Autor:
Dagmar Solichová, Vladimír Bláha, Siroký O, Martin Blažek, Stanislav Filip, Melanie Cermanová, Jaroslav Malý, Vít Řeháček, Milan Bláha
Publikováno v:
Therapeutic Apheresis and Dialysis. 11:9-15
The aim of this work is to arbitrate the incidence of side effects and tolerability of long lasting LDL-apheresis in familial hyperlipoproteinemia. 1200 procedures were performed and the last 463 of them were evaluated. An immunoadsorption method of
Publikováno v:
Skull Base. 8:215-219
A case of a xanthogranuloma arising in the anterior skull base involving the bone of the left orbital roof, the dura mater, and the periorbit is presented. The lesion was completely removed by a supraorbital “eyebrow” skin incision using frameles
Publikováno v:
Clinical Neurology and Neurosurgery. 96:79-82
Intracranial xanthomata occurring in patients with familial hypercholesterolemia are very rare. We present a young woman with a large intracranial xanthoma. The patient was treated for a familial hyperlipoproteinemia type IIa. MRI and morphological f
Autor:
John J. Fung, Thomas E. Starzl
Liver transplantation was the product of five interlocking themes. These began in 1958-1959 with canine studies of then theoretical hepatotrophic molecules in portal venous blood (Theme I) and with the contemporaneous parallel development of liver an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15113fc6356b4c2794b8af4c468f4b28
https://europepmc.org/articles/PMC4507423/
https://europepmc.org/articles/PMC4507423/
Publikováno v:
Clinical Chemistry. 46:722-724
Apolipoprotein (apo) E is a M r 34 000 plasma protein involved in lipid metabolism (1) and is genetically polymorphic. There are three common codominant alleles, designated e2 , e3 , and e4 (2). The genetic basis of the common alleles lies within cod