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Auswahl der wissenschaftlichen Literatur zum Thema „Hypercholesteremia“
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Zeitschriftenartikel zum Thema "Hypercholesteremia"
Visavadiya, Nishant P., und A. V. R. L. Narasimhacharya. „AsparagusRoot Regulates Cholesterol Metabolism and Improves Antioxidant Status in Hypercholesteremic Rats“. Evidence-Based Complementary and Alternative Medicine 6, Nr. 2 (2009): 219–26. http://dx.doi.org/10.1093/ecam/nem091.
Der volle Inhalt der QuelleKhan, Safi U., und Khurram Nasir. „Hypercholesteremia in Indigenous Population“. JACC: Advances 2, Nr. 3 (Mai 2023): 100352. http://dx.doi.org/10.1016/j.jacadv.2023.100352.
Der volle Inhalt der QuelleNordin, Jenizan, und Ahmad Badruddin Ghazali. „Osteonecrosis of the jaw in patients taking Atorvastatin: Case series“. IIUM Journal of Orofacial and Health Sciences 3, Nr. 2 (30.07.2022): 219–22. http://dx.doi.org/10.31436/ijohs.v3i2.73.
Der volle Inhalt der QuelleKamalova, Aelita A. „Diet Therapy in Children with Hypercholesteremia“. Current Pediatrics 19, Nr. 4 (19.09.2020): 309–15. http://dx.doi.org/10.15690/vsp.v19i4.2140.
Der volle Inhalt der QuelleDietrich, Hans H. „Apolipoprotein E in Hypercholesteremia and Beyond“. Stroke 38, Nr. 7 (Juli 2007): 2036. http://dx.doi.org/10.1161/strokeaha.107.489856.
Der volle Inhalt der QuelleLEWIS, S. „P514 Hypercholesteremia induces baroreceptro reflex dysfunction“. European Heart Journal 24, Nr. 5 (März 2003): 81. http://dx.doi.org/10.1016/s0195-668x(03)93952-2.
Der volle Inhalt der QuelleNAKAI, TSUGUHIKO. „Familial hypercholesteremia complicated by nephrotic syndrome.“ Nihon Naika Gakkai Zasshi 79, Nr. 8 (1990): 1079–80. http://dx.doi.org/10.2169/naika.79.1079.
Der volle Inhalt der QuelleHURLEY, D. „Hypercholesteremia induces enhanced circulating inflammatory activity“. American Journal of Hypertension 17, Nr. 5 (Mai 2004): S242. http://dx.doi.org/10.1016/j.amjhyper.2004.03.648.
Der volle Inhalt der QuelleLi, Nan F., Hong M. Wang, Jin Yang, Ling Zhou, Xiao G. Yao und Jing Hong. „Serum uric acid is associated with metabolic risk factors for cardiovascular disease in the Uygur population“. Applied Physiology, Nutrition, and Metabolism 34, Nr. 6 (Dezember 2009): 1032–39. http://dx.doi.org/10.1139/h09-101.
Der volle Inhalt der QuelleKawsar, Dr Syeda Masuma, und Dr Amirul Islam Bhuyan. „Outcome of Heart Rate and Blood Pressure of a Patient after Successful Coronary Angioplasty and Stenting“. Scholars Journal of Applied Medical Sciences 11, Nr. 03 (30.03.2022): 668–71. http://dx.doi.org/10.36347/sjams.2023.v11i03.031.
Der volle Inhalt der QuelleDissertationen zum Thema "Hypercholesteremia"
Staples, Heidi. „The effect of lipid-lowering pharmacotherapy on concurrent diet and exercise behaviors /“. Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=31543.
Der volle Inhalt der QuelleIt was therefore hypothesized that pharmacologically-treated patients with untreated hypercholesterolemia started on a program of lifestyle modification would achieve relatively less reduction in dietary fat intake and body weight, and participate less often in physical activity, if a pharmacologic agent was simultaneously prescribed. This was tested by a protocol in which these and related variables were assessed in participants who thought they were taking a lipid-lowering medication at diagnosis, compared to conventional initial treatment of diet and exercise alone. (Abstract shortened by UMI.)
Collins, Melissa. „Effects of plant sterols and exercise training on apolipoprotein A and B, adiponectin, growth hormone and ghrelin in hypercholesterolemic sedentary adults“. Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=99331.
Der volle Inhalt der QuelleVergotine, Joseph Vincent. „The MED-PED project : presymptomatic diagnosis in families with disease- related LDL receptor gene mutations“. Thesis, Stellenbosch : Stellenbosch University, 2000. http://hdl.handle.net/10019.1/51997.
Der volle Inhalt der QuelleENGLISH ABSTRACT: Familial hypercholesterolaemia (FH) contributes significantly to the high death rate from cardiovascular disease worldwide. FH is a common autosomal co-dominant disease characterised by raised cholesterol levels and premature coronary heart disease (CHD). Whilst these features usually are very prominent in homozygotes the clinical diagnosis of heterozygotes is complicated by variable phenotypic expression. Specific founder genes in the low-density lipoprotein receptor (LDLR) gene have increased the prevalence of FH in South African Afrikaners, Indians, Jews and Coloureds, and screening for these known mutations allows unequivocal diagnosis of FH-affected individuals. The systematic molecular analysis of FH resulted in the identification of at least ten founder-type LDLR gene mutations among the 56 different gene defects described to date in the diverse South African population. DNA screening of 792 at-risk family members for the FH-related mutations identified in 379 index cases, allowed accurate disease diagnosis in an additional 340 relatives and exclusion of the relevant mutation in 452 individuals. This effort forms part of the MED PED FH initiative, a collaborative project to "Make Early Diagnosis and Prevent Early Deaths in MEDical PEDigrees with FH". Evaluation of clinical criteria versus DNA diagnosis of three founder-related mutations (D154N, D206E and V408M) in the South African population demonstrated that the sensitivity and specificity of diagnoses, based on total cholesterol values measured in family members of index cases recruited for this study, were 88% and 77%, respectively. A population-directed DNA diagnosis of FH is therefore justified in South Africa on a routine basis, since expression of the defective gene measured in biochemical tests does not allow accurate diagnosis of FH in all cases. The application of mutation detection was illustrated by prenatal diagnosis of FH performed for a couple who are both heterozygous for the most common Afrikaner mutation, D206E. The mutation was absent in the foetus and a normocholesterolaemic infant was born. Prenatal diagnosis of FH, aimed at the detection of homozygous cases, is particularly applicable in populations and families with molecularly defined LDLR gene mutations. The MED-PED approach resulted in accurate diagnosis and subsequent treatment of FH in more patients, and referral to lipid clinics where they could receive the intensive care their condition justifies. Molecularly diagnosed FH patients will be the first to benefit from future treatment approaches based on mutation type.
AFRIKAANSE OPSOMMING: Familiële hiprcholesterolemie dra grootliks by tot die wêreldwye hoë sterftesyfer van kardiovaskulêre siekte. FH is 'n algemene outosomale ko-dominante siekte wat gekenmerk word deur verhoogde cholesterolvlakke en vroeë koronêre hartsiekte. Terwyl hierdie kenmerke prominent is in homosigote, word die kliniese diagnose van heterosigote bemoeilik deur variasie in fenotipiese uitdrukking. Spesifieke stigtergene in die lae-digtheids lipoproteien reseptor (LDLR) geen het die voorkomssyfer van FH verhoog in Suid Afrikaanse Afrikaners, Indiërs, Jode en Kleurlinge. Sifting vir hierdie bekende mutasies maak akkurate diagnose van FH geaffekteerde individue moontlik. Die sistematiese molekulêre analise van FH het aangetoon dat ten minste tien van die 56 verskillende geen defekte wat tot dusver beskryf is in die Suid-Afrikaanse populasie stigtertipe LDLR geen mutasies is. DNA sifting van 792 familielede vir die FH-verwante mutasie in 379 indeksgevalle geïdentifiseer is, het akkurate diagnose moontlik gemaak in 340 addisionele familielede, en uitsluiting daarvan in 452 individue. Hierdie poging vorm deel van die MED-PED FH ("Make Early Diagnosis and Prevent Early Deaths in MEDical PEDigrees with FH) inisiatief. Evaluering van kliniese kriteria teenoor DNA diagnose van drie stigter verwante mutasies (D154N, D206E en V408M) in die Suid Afrikaanse populasie het getoon dat die sensitiwiteit en spesifisiteit van die diagnose, wat gebasseer is op totale cholesterol waardes in familielede van indeksgevalle, onderskeidelik 88% en 77% was. 'n Populasie gerigte DNA diagnose van FH is dus geregverdig in Suid-Afrika op "n roetine basis, omdat die defektiewe geen nie altyd in biochemiese toetse uitgedruk word nie. Die waarde van mutasie opsporing is geillustreer deur 'n voorgeboortelike diagnose van FH wat aangevra is vir ouers wat beide heterosigoties is vir die mees algemene Afrikaner mutasie, D206E. Die mutasie was afwesig in die fetus en 'n normocholesterolemiese baba is gebore. Voorgeboortelike diagnose van FH, wat gemik is op die opsporing van homosigotiese gevalle, is veral van toepassing in populasies en families met bekende LDLR geen mutasies. Die MED-PED benadering het gelei tot akkurate diagnose en daaropvolgende behandeling van FH in meer pasiënte, en verwysings na lipiedklinieke waar hulle intensiewe aandag kan geniet. Molekulêre gediagnoseerde FH pasiënte sal die eerste wees om baat te vind by toekomstige behandeling wat moontlik gebasseer sal word op mutasie status.
Wong, Kwok-kit Sunny. „A study of DNA mutations in LDL receptor gene of Chinese patients with familial hypercholesterolaemia /“. Hong Kong : University of Hong Kong, 1997. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19109878.
Der volle Inhalt der QuelleSt-Onge, Marie-Pierre. „Effect of kefir supplementation on blood lipid parameters in free-living hypercholesterolemic men“. Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape9/PQDD_0024/MQ50885.pdf.
Der volle Inhalt der QuelleMiller, Stephanie M. „The Relationship of Waist Size to Blood Pressure and Cholesterol Among College Students“. Lynchburg, Va. : Liberty University, 2007. http://digitalcommons.liberty.edu.
Der volle Inhalt der QuelleYang, Tat-chi Teddy. „Effect of Chinese green tea on diet-induced hypercholesterolemia and arteriosclerosis in rats /“. Hong Kong : University of Hong Kong, 1998. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19657560.
Der volle Inhalt der QuelleNeubauer, Tamara E. „Cholesterol reduction in men : an experimental investigation of intensive treatment with frequent feedback versus a simple educational treatment /“. Thesis, This resource online, 1990. http://scholar.lib.vt.edu/theses/available/etd-03122009-040807/.
Der volle Inhalt der QuelleMatthan, Nirupa Rachel. „Impact of hydrogenated fat consumption on in vivo lipid metabolism in moderately hypercholesterolemic women“. Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape4/PQDD_0033/NQ64617.pdf.
Der volle Inhalt der QuelleFourie, Anne Madeleine. „The expression and metabolism of low density lipoprotein receptors in familial hypercholesterolaemia“. Doctoral thesis, University of Cape Town, 1989. http://hdl.handle.net/11427/27174.
Der volle Inhalt der QuelleBücher zum Thema "Hypercholesteremia"
National Cholesterol Education Program (U.S.). Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults., Hrsg. Report of the Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. [Bethesda, Md.]: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1989.
Den vollen Inhalt der Quelle findenHuang, Zhaosheng. Fei pang bing zhi fang gan yu gao zhi xue zheng Zhong Xi yi zhen liao yu tiao yang =: Obesity fat liver and high-lipidemia. Xianggang: Tian heng wen hua chu ban gong si, 2001.
Den vollen Inhalt der Quelle findenNational, Cholesterol Education Program (U S. ). Expert Panel on Detection Evaluation and Treatment of High Blood Cholesterol in Adults. Third report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (adult treatment panel III): Final report. [Washington, D.C.]: The Program, 2002.
Den vollen Inhalt der Quelle findenMcCord, Holly. Win the cholesterol war: 100 real-life secrets to trimming points (and pounds). New York: Berkley Books, 2003.
Den vollen Inhalt der Quelle findenWin the cholesterol war: 100 real-life secrets to trimming points (and pounds). New York: Berkley Books, 2003.
Den vollen Inhalt der Quelle findenNational Cholesterol Education Program (U.S.). Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Second report of the Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (adult treatment panel II). [Bethesda, Md.?]: National Cholesterol Education Program, National Institute of Health, National Heart, Lung, and Blood Institute, 1993.
Den vollen Inhalt der Quelle findenNational Cholesterol Education Program (U.S.), Hrsg. Third report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (adult treatment panel III): Executive summary. [Bethesda, Md.]: National Cholesterol Education Program, National Heart, Lung, and Blood Institute, National Institutes of Health, 2001.
Den vollen Inhalt der Quelle findenMcCord, Holly. Win the cholesterol war: 100 real-life secrets to trimming points (and pounds). New York: Berkley Books, 2003.
Den vollen Inhalt der Quelle findenWetherill, Douglas. High cholesterol. Cincinnati, OH: Betterway Books, 2000.
Den vollen Inhalt der Quelle findenR, Gordon Bruce, und Gotto Antonio M, Hrsg. The Treatment of severe hypercholesterolemia-- can we impact disease course?: Proceedings of a symposium, November 9, 1991, Anaheim, California. Princeton, NJ: Excerpta Medica, 1992.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Hypercholesteremia"
Loria, Roger M. „Effect of Dietary Hypercholesteremia on Host Immune Response“. In Nutrients, Stress, and Medical Disorders, 267–78. Totowa, NJ: Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-952-4:267.
Der volle Inhalt der QuelleHunninghake, D. B., D. M. Hibbard, W. C. Duane, M. L. Freeman, W. F. Prigge, K. J. Graham und R. L. Gebhard. „Metabolic Studies with Lovastatin in Patients with Primary Hypercholesteremia“. In Drugs Affecting Lipid Metabolism, 150–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71702-4_27.
Der volle Inhalt der QuelleWisnu Murti, Tridjoko. „Fermentation of Bovine, Non-Bovine and Vegetable Milk“. In Fermentation - Processes, Benefits and Risks. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96699.
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