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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. Homozygous Familial Hypercholesterolemia (le) Somwanshi PR, Agarwal NS - Indian
    familial hypercholesterolemia (FH) is a condominant genetic disorder that occursin the heterozygous form in 1500 of the European and American population.  
    http://www.ijdvl.com/article.asp?issn=0378-6323;year=2000;volume=66;issue=6;spag

82. Obstetrics & Gynecology -- Sign In Page
    Children with familial hypercholesterolemia have endothelial dysfunction andincreased carotid intimamedia thickness (IMT), which herald the premature  
    http://www.greenjournal.org/cgi/content/full/104/4/862
    
    Extractions: This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Alert me to new issues of the journal Download to citation manager To view this item, select one of the options below: Sign In User Name Sign in without cookies.

83. Apob100 Metabolism In Familial Hypercholesterolemia - VRR
    Translate this page apolipoprotein b100, familial hypercholesterolemia, hmg coa reductase inhibitors,ldl receptor, lipoprotein metabolism. Chercheur(s)  
    http://www.vrr.ulaval.ca/bd/projet/fiche/76061.html

84. Familial Hypercholesterolemia
    familial hypercholesterolemia. Examinations Photographs Movies Links Home SearchnoJava Home.  
    http://medgen.genetics.utah.edu/photographs/pages/familial_hypercholesterolemia.

85. LDLR: Low Density Lipoprotein Receptor (familial Hypercholesterolemia)
    LDLR low density lipoprotein receptor (familial hypercholesterolemia). COMMON PARCSNP DATA Chromosomal Location 19p13.3. GeneSpecific Links LocusLink  
    http://droog.gs.washington.edu/parc/data/ldlr/welcome.html
    
    Extractions: SNP Sequence Context A multi-entry FASTA file containing each polymorphic site and 50 bp of flanking sequence both 5' and 3'. Each polymorphic position is listed according to the IUPAC ambiguity codes or the insertion allele at that site. SNP Allele Frequency Frequency of each allele at each polymorphic site. Allele frequencies are listed for each sample population and the combined samples. The last three columns list the heterozygosity for each polymorphic site (hz). Color FASTA Sequence The final reference sequence generated for this gene as a colored FASTA sequence in order to easily locate gene features. Variations are shown in red, exons are shown in blue, and protein translations are included in the coding regions. SITE SPECIFIC DATA SNP Locations Mapping of each SNP onto the gene structure. Each SNP can be listed as: - (noncoding), 5UT (5'UTR), 3UT (3'UTR). If a SNP occurs in a coding region its effect on the amino acid translation is shown. All translations are done from the Locus Link RefSeq curated mRNA sequence (Acc. No.: NM* or XM*) for each gene.

86. Familial Hypercholesterolemia
    A dominantly inherited genetic condition that results in markedly elevated (lowdensitylipoprotein) cholesterol levels beginning at birth, and resulting in  
    http://www.shands.org/health/information/000392.htm
    
    Extractions: Causes, incidence, and risk factors: Affected people have consistently high levels of low-density lipoprotein, which leads to premature atherosclerosis of the coronary arteries. Typically in affected men, heart attacks occur in their 40s to 50s, and 85% of men with this disorder have experienced a heart attack by age 60. The incidence of heart attacks in women with this disorder is also increased, but delayed 10 years later than in men.

87. FHC Pedigree
    familial hypercholesterolemia FHC. The pedigree to the right shows the inheritanceof FHC over three generations. The affected gene which is located on  
    http://www.people.virginia.edu/~rjh9u/fhcped.html

88. FAMILIAL HYPERCHOLESTEROLEMIA
    familial hypercholesterolemia A relatively rare (7 out of 1000) genetic diseasein which there is elevation in the blood triglycerides, cholesterol,  
    http://www.medhelp.org/glossary2/new/GLS_2002.HTM

89. HUGO HGM2003 - Presentation 16 - A Mexican Kindred With Familial Hypercholestero
    A Mexican kindred with familial hypercholesterolemia linked to chromosome 1p32 Heterozygous familial hypercholesterolemia (FH) is an inherited metabolic  
    http://hgm2003.hgu.mrc.ac.uk/Abstracts/Publish/WorkshopOrals/Workshop02/hgm016.h
    
    Extractions: Unidad de Biología Molecular y Medicina Genómica, Instituto de Investigaciones Biomédicas de la Universidad Nacional Autónoma de México e Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City Departamento de Endocrinología y Metabolismo de Lípidos, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City Departments of Biochemistry and Molecular Biology, Medicine and Human Genetics, The University of Chicago, Chicago, USA. Other abstracts in same session

90. CMAJ -- Please Take Our Questionnaire
    familial hypercholesterolemia (FH) is characterized by the accumulation of excess The LDL receptor locus in familial hypercholesterolemia mutational  
    http://www.cmaj.ca/cgi/content/full/172/4/495
    
    Extractions: Fall 2005 online survey of eCMAJ users For 50 weeks of the year, eCMAJ is available full-text online, free of charge and without registration. For 2 weeks only, from Sept. 7th to Sept. 18th, the price of admission is completion of a short survey. This survey will help us to understand more about our visitors and will take a maximum of 5 minutes to complete. You will have to fill it out only once from the computer you are now using, as long as you have cookies enabled in your Web browser. If you don't have time to complete the survey right now, click here for access to eCMAJ. We'll ask you again at your next visit. Your cookies need to be enabled for this to work properly. If you have already answered this survey, click here to access eCMAJ. Your cookies need to be enabled for this to work properly. If you have difficulties with this survey, please e-mail for assistance. cliquez ici cliquer ici pour obtenir de l'aide.

91. Homozygous Familial Hypercholesterolemia
    Homozygous familial hypercholesterolemia drug treatment.  
    http://browse.drugs.com/cond-homozygous_familial_hypercholesterolemia.html

92. Coronary Artery Disease In Heterozygous Familial Hypercholesterolemia Patients W
    Background familial hypercholesterolemia (FH), an autosomal codominant disease, Genetic Diagnosis of familial hypercholesterolemia in a South European  
    http://circ.ahajournals.org/cgi/content/abstract/92/3/290
    
    Extractions: This Article Full Text Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Request Permissions PubMed PubMed Citation Articles by Davignon, J. Circulation. J. Lambert, PhD S. Lussier-Cacan, PhD J. Davignon, MD, MSc Correspondence to Dr S. Lussier-Cacan, Hyperlipidemia and Atherosclerosis Research Group, Clinical Research Institute of Montreal, 110 Pine Ave W, Montreal, Quebec, Canada H2W 1R7. Background Familial hypercholesterolemia (FH), an autosomal codominant disease, is characterized by high levels of LDL cholesterol and a high incidence of coronary artery disease (CAD). To date, genetic heterogeneity has hindered the proper assessment of the relation between risk factors and CAD in FH patients. Methods and Results We studied the association between CAD and common risk factors in a sample of 263 French Canadian FH patients the LDL receptor gene. Thirty-five women and 54 men had CAD.

93. Coronary Artery Disease In Heterozygous Familial Hypercholesterolemia Patients W
    familial hypercholesterolemia (FH) is characterized by markedly elevated LDLC Clinical and Biological Features of 147 familial hypercholesterolemia  
    http://circ.ahajournals.org/cgi/content/full/92/3/290
    
    Extractions: This Article Abstract Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Request Permissions PubMed PubMed Citation Articles by Davignon, J. Circulation. J. Lambert, PhD S. Lussier-Cacan, PhD J. Davignon, MD, MSc Correspondence to Dr S. Lussier-Cacan, Hyperlipidemia and Atherosclerosis Research Group, Clinical Research Institute of Montreal, 110 Pine Ave W, Montreal, Quebec, Canada H2W 1R7. Background Familial hypercholesterolemia (FH), an autosomal codominant disease, is characterized by high levels of LDL cholesterol and a high incidence of coronary artery disease (CAD). To date, genetic heterogeneity has hindered the proper assessment of the relation between risk factors and CAD in FH patients.

94. Risk Of Fatal Stroke In Patients With Treated Familial Hypercholesterolemia. A P
    familial hypercholesterolemia, Peripheral Arterial Disease, FamilialHypercholesterolemia and Coronary Heart Disease A HuGE Association Review  
    http://stroke.ahajournals.org/cgi/content/abstract/01.STR.0000047123.14312.3Ev1
    
    Extractions: 01.STR.0000047123.14312.3Ev1 Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Request Permissions PubMed PubMed Citation Articles by Huxley, R. R. Articles by for the Simon Broome Familial Hyperlipidaemia Register Group and Scientific Steering Committee, Related Collections Epidemiology

95. Familial Hypercholesterolemia
    Lausnaleitanám verklegt nám - familial hypercholesterolemia HypercholesterolemiaAtherosclerosis Arcus senilis Xanthomas. Myndin er héðan eMedicine  
    http://www.hi.is/nam/lifsam/Sameindadeild/Reynir/Familial hypercholesterolemia.h

96. Familial Hypercholesterolemia Spurningar
    Lausnaleitanám verklegt nám - familial hypercholesterolemia spurningar Heimild Goldstein JL, Hobbs, Brown MS (2001). familial hypercholesterolemia.  
    http://www.hi.is/nam/lifsam/Sameindadeild/Reynir/Familial hypercholesterolemia.s

97. Familial Hypercholesterolemia (Disease) - Detroit, Michigan
    familial hypercholesterolemia (Disease) courtesy of Henry Ford Health Systemof Detroit, Michigan.  
    http://www.henryfordhealth.org/14870.cfm
    
    Extractions: Coronary artery blockage Definition A dominantly inherited genetic condition that results in markedly elevated LDL (low-density lipoprotein) cholesterol levels beginning at birth, and resulting in heart attacks at an early age. Alternative Names Type II hyperlipoproteinemia; Hypercholesterolemic xanthomatosis; Low density lipoprotein receptor mutation Causes And Risk Affected people have consistently high levels of low-density lipoprotein, which leads to premature atherosclerosis of the coronary arteries. Typically in affected men, heart attacks occur in their 40s to 50s, and 85% of men with this disorder have experienced a heart attack by age 60. The incidence of heart attacks in women with this disorder is also increased, but delayed 10 years later than in men.

98. Renin-Angiotensin System Polymorphisms And Coronary Events In Familial Hyperchol
    Key Words familial hypercholesterolemia • coronary artery disease Familialhypercholesterolemia (FH) is an autosomal dominant disorder of clearance of  
    http://hyper.ahajournals.org/cgi/content/full/36/5/808
    
    Extractions: This Article Abstract Full Text (PDF) Alert me when this article is cited ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Request Permissions PubMed PubMed Citation Articles by Wierzbicki, A. S. Articles by Crook, M. A. Related Collections Chronic ischemic heart disease Abstract as risk factors for coronary heart disease (CHD) is controversial. This study investigated their role in patients with heterozygous familial hypercholesterolemia (FH). Polymorphism frequencies (ACE I/D), angiotensinogen M235T, and angiotensin-II type I receptor (AG2R) A1166C were determined in 112 patients with FH and 72 patients with polygenic hypercholesterolemia, of

99. Compound Heterozygous Familial Hypercholesterolemia And Familial Defective Apoli
    Background familial hypercholesterolemia (FH) and familial defective apolipoproteinB100 (FDB) represent ligand-receptor disorders that are complementary.  
    http://www.clinchem.org/cgi/content/abstract/47/3/438
    
    Extractions: This Article Full Text Full Text (PDF) Submit a response ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Download to citation manager PubMed PubMed Citation Articles by Tai, E. S. Articles by Tan, C. E. Related Collections Heart Health and the Clinical Laboratory Clinical Chemistry. E. Shyong Tai ,a Evelyn S.C. Koay Edmund Chan Tzer Jing Seng Lih Ming Loh Sunil K. Sethi and Chee Eng Tan

100. Serum Lipoprotein(a) In Patients Heterozygous For Familial Hypercholesterolemia,
     Lipoprotein(a) in Homozygous familial hypercholesterolemia Coronary ArteryDisease in Heterozygous familial hypercholesterolemia Patients With the Same  
     http://atvb.ahajournals.org/cgi/content/abstract/11/4/940
     
     Extractions: This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Request Permissions PubMed PubMed Citation Articles by Mbewu, A. D. Articles by Miller, J. P. AD Mbewu, D Bhatnagar, PN Durrington, L Hunt, M Ishola, S Arrol, M Mackness, P Lockley and JP Miller University of Manchester Department of Medicine, Manchester Royal Infirmary, UK. Serum lipoprotein(a) (Lp[a]) levels were significantly higher in 89 patients with heterozygous familial hypercholesterolemia (FH) (geometric mean, 22.7 mg/dl) than in 109 normocholesterolemic controls (10.0 mg/dl, p less than 0.05) and 40 controls (9.1 mg/dl, p less than 0.05) with similarly elevated low density lipoprotein cholesterol levels due to other primary hypercholesterolemias. To provide further evidence that the

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