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Familial Hypercholesterolemia:     more books (15)

Familial Hypercholesterolemia - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-10-01 Familial Hypercholesterolemia by Frederic P. Miller, Agnes F. Vandome, et all 2010-01-19 Complex Genetics of Monogenic Familial Hypercholesterolemia by K. C. M. C. Koeijvoets, 2007 Statin reverses atherogenesis in highest-risk kids familial hypercholesterolemia.(Children's Health): An article from: Family Practice News by Bruce Jancin, 2004-02-01 Towards Genetic Prediction of Coronary Heart Disease in Familial Hypercholesterolemia by Jeroen Van Der Net, 2009 Familial hypercholesterolemia: genetic predisposition to atherosclerosis.(Advanced Practice): An article from: MedSurg Nursing by Mary B. Engler, 2004-08-01 Statin reverses atherogenesis in highest-risk children: familial hypercholesterolemia.: An article from: Pediatric News by Bruce Jancin, 2004-02-01 Lipid Disorders: Low-Density Lipoprotein, Cholesterol, High-Density Lipoprotein, Triglyceride, Familial Hypercholesterolemia, Lipoprotein(a) Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.: An article from: Human Biology by Erardo Merino-Ibarra, Sergio Castillo, et all 2005-10-01 ACAT Inhibition and Progression of Carotid Atherosclerosis in Patients With Familial Hypercholesterolemia: The CAPTIVATE Randomized Trial / Religious Coping and Use of Intensive Life-Prolonging Care Near Death in Patients With Advanced Cancer (JAMA: The Journal of the American Mediacl Association, Volume 301, Number 11, March 18, 2009) by M. C. Meuwese, 2009 Ultrasound Measurement of Intima-media Thickness and Atherosclerotic Plaques in Carotid and Femoral Arteries (Methodological Studies & a Five-year Observational Study in Familial Hypercholesterolemia) by Inger Wendelhag, 1995 Familial hypercholesterolemia and other disorders of lipoprotein metabolism (Medical Grand Rounds) by Joseph L Goldstein, 1979 A familial-racial analysis of serum cholesterol and triglyceride levels by Jess David Curb, 1973 Lowering plasma cholesterol by raising LDL receptors (Medical Grand Rounds) by Michael S Brown, 1981

lists with details

81. HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA IS ASSOCIATED WITH LARGER LDL SIZE FO
    157, Return to Table of Contents. HETEROZYGOUS familial hypercholesterolemia IS ASSOCIATED WITH LARGER LDL SIZE FOR ANY GIVEN FASTING TRIGLYCERIDE CONCENTRATION.  
    http://www.ccs.ca/society/congress2002/abstracts/abs/a157.htm
    
    Extractions: OBJECTIVES: Familial hypercholesterolemia (FH) is a genetic disorder associated with raised plasma LDL-cholesterol levels and premature coronary heart disease (CHD). Although it has been suggested that LDL size could further increase the CHD risk resulting from an elevated LDL concentration, factors controlling LDL size in FH patients are not fully understood. Therefore, the objectives of the present study were to compare LDL size in FH vs nonFH patients and to study its relationship with known correlates of LDL size such as abdominal obesity (waist girth) and triglyceride (TG) levels. METHODS: After exclusion of patients with fasting TG and glucose levels greater than 4.5 mmol/L and 7.0 mmol/L respectively, a sample of 112 male patients (46.7 ± 12.6 years of age) with a clinical and/or molecular diagnosis of heterozygous FH was compared to a group of 305 nonFH men (42.3 ± 11.9 years). LDL size was assessed by 2-16% polyacrylamide gel electrophoresis. RESULTS: FH patients were characterized by the expected differences in their plasma lipid profile including substantially higher cholesterol (+65.8%), LDL-cholesterol (+88.9%) and apo B (+30.6%) levels than non FH men despite the fact that they had lower body mass index (-8.1%) and waist circumference (-5.4%) values than nonFH controls (p

82. PillSupplier.com - Conditions And Diseases/Genetic Disorders/Familial Hyperchole
    Category familial hypercholesterolemia. HOME Login . Conditions and Diseases/Genetic Disorders/familial hypercholesterolemia. Links  
    http://www.pillsupplier.com/dir/839/

83. Entrez PubMed
    Click here to read Increased prevalence of coronary ectasia in heterozygous familial hypercholesterolemia. Sudhir K, Ports TA, Amidon  
    http://www.thrombosisjournal.com/pubmed/7867176
    
    Extractions: Summary Brief Abstract Citation ASN.1 MEDLINE XML UI List LinkOut Related Articles Cited in Books CancerChrom Links Domain Links 3D Domain Links GEO DataSet Links Gene Links Genome Links GEO Links HomoloGene Links Nucleotide Links OMIM Links PMC Links Cited in PMC PopSet Links Protein Links SNP Links Structure Links UniSTS Links Show: Sort Author Journal Pub Date Text File Clipboard E-mail Order

84. Familial Hypercholesterolemia - Encyclopedia Article About Familial Hypercholest
    encyclopedia article about familial hypercholesterolemia. familial hypercholesterolemia in Free online English dictionary, thesaurus and encyclopedia.  
    http://encyclopedia.thefreedictionary.com/Familial hypercholesterolemia
    
    Extractions: Dictionaries: General Computing Medical Legal Encyclopedia Word: Word Starts with Ends with Definition In medicine This article is about medical science and practice. For substances that treat patients, see drugs, medication and pharmacology Note to contributors: This article is about medicine in general. Please add contributions to medical topics to their individual articles. Medicine is a branch of health science concerned with restoring and maintaining health and wellness. Broadly, it is the practical science of preventing and curing diseases. However, Medicine often refers more specifically to matters dealt with by physicians and surgeons. Click the link for more information. familial hypercholesterolemia is a rare disease An orphan or rare disease is generally considered to have a prevalence of less than 5% affected individuals in the society. Certain diseases with more than 5% affected individuals are included, but subpopulations of these conditions may be less than the prevalence standard for rare disease. See also List of common diseases.

85. Project: Pediatric Implications Of Heterozygous Familial Hypercholesterolemia (N
    impli . entire NIWI site (en), Help. Project Pediatric implications of heterozygous familial hypercholesterolemia. switch to nl. mutation.  
    http://www.niwi.knaw.nl/en/oi/nod/onderzoek/OND1241505/toon

86. Blackwell Synergy - Cookie Absent
    Report. familial hypercholesterolemia (Type IIb) in a child a case report with interesting features. PVS Prasad, MBBS, DV, DD, MD, and N. Chidambaram, MBBS, MD.  
    http://www.blackwell-synergy.com/links/doi/10.1111/j.1365-4632.2004.01457.x/full
    
    Extractions:  Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

87. Thieme-connect - Abstract
    familial hypercholesterolemia in South Africa. KEYWORDS. familial hypercholesterolemia cardiovascular disease - homozygous FH - South Africa.  
    http://www.thieme-connect.com/ejournals/abstract/svm/doi/10.1055/s-2004-822991
    
    Extractions: Familial Hypercholesterolemia in South Africa Adrian David Marais  M.B.Ch.B.  F.C.P.(SA) , Jean Catherine Firth  M.B.Ch.B.  D.C.H. , Dirk Jacobus Blom  M.B.Ch.B.  M.Med.  F.C.P.(SA)  Lipidology Division of Internal Medicine and MRC Cape Heart Group, University of Cape Town Health Science Faculty, Observatory, South Africa. South Africa, especially the Caucasian part of the population, has one of the highest incidences of familial hypercholesterolemia in the world. The founder effect in this region has led to this high incidence and to a limited number of mutations in the low-density lipoprotein-receptor gene. This chapter describes current situation concerning the management of familial hypercholesterolemia in South Africa. Familial hypercholesterolemia - cardiovascular disease - homozygous FH - South Africa Full Text as

88. Thieme-connect - Abstract
    Homozygous familial hypercholesterolemia and Its Management. Mutations in the lowdensity lipoprotein (LDL) receptor gene cause familial hypercholesterolemia.  
    http://www.thieme-connect.com/ejournals/abstract/svm/doi/10.1055/s-2004-822985
    
    Extractions: Homozygous Familial Hypercholesterolemia and Its Management Adrian David Marais  M.B.Ch.B.  F.C.P.(SA) , Jean Catherine Firth  M.B.Ch.B.  D.C.H. , Dirk Jacobus Blom  M.B.Ch.B.  M.Med.  F.C.P.(SA)  Lipidology Division of Internal Medicine and MRC Cape Heart Group, University of Cape Town Health Science Faculty, Observatory, South Africa Homozygous familial hypercholesterolemia - low-density lipoprotein - plasmapheresis - statins Full Text as

89. Homozygous Familial Hypercholesterolemia - Evaluation, Treatment And Research At
    The National Heart, Lung and Blood Institute is actively seeking patients with Homozygous familial hypercholesterolemia to receive free evaluation and/or  
    http://patientrecruitment.nhlbi.nih.gov/LDL500.aspx
    
    Extractions: LDL > 500 mg/dL Research Study If you have homozygous familial hypercholesterolemia (FH), you are invited to participate in a study that will evaluate the development and follow the natural history of atherosclerosis in your disorder. A variety of clinical and research techniques will be used to assess and follow the development of atherosclerosis. Recommendations for treatments will be provided based upon these findings. Persons with homozygous familial hypercholesterolemia typically have a total and low density lipoprotein (LDL) cholesterol concentration greater than 700 mg/dL with normal triglycerides. Cholesterol deposits called xanthomas are frequently present in the first few years of life and are located on the elbows, knees, between the webs of the fingers and on the Achilles tendons. Eligible persons will undergo a comprehensive cardiac evaluation. All patients will remain under the care of their own physician who will receive results of the laboratory and diagnostic tests. In most cases, you will be invited back for yearly evaluations. There is no cost to you for travel or medical testing.

90. Entrez PubMed
    2001 Jun;8(6)4768. Click here to read Implications for familial hypercholesterolemia from the structure of the LDL receptor YWTD-EGF domain pair.  
    http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?holding=npg&cmd=Retrieve&db=PubMed

91. Redirect
    http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?143890

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