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

HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription to Full Text Efficacy and safety of statin therapy in children with familial hypercholesterolemia:... Obstet Gynecol. 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. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 1 day for US$20.00 Regain Access - You can regain access to a recent Pay per Article purchase if your access period has not yet expired. Sign Up Subscribe to the Journal - Subscribe to the print and/or online journal. HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH

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

Accueil À propos Nous joindre Plan du site ... Chercher Chercher dans cette section : AVANCÉE Apob100 Metabolism in familial hypercholesterolemia Subvention Fondation des maladies du coeur du Canada Subventions pour projet de recherche Description Domaine(s) de recherche Cardiologie et hématologie Endocrinologie Mot(s)-clé(s) apolipoprotein b100, familial hypercholesterolemia, hmg coa reductase inhibitors, ldl receptor, lipoprotein metabolism Chercheur(s) Patrick Couture , Médecine, Département de médecine, responsable du projet Benoît Lamarche , Sces agriculture et alimentation, Dép. sciences aliments et nutrition Tranche(s) de financement Fondation des maladies du coeur du Québec Année En espèces Totaux : Date de début : Date de fin : Fiche numéro : Dernière mise à jour : 5 juillet 2005 Demande de correction

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

familial hypercholesterolemia Examinations Photographs Movies Links ... noJava Home

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

LDLR: low density lipoprotein receptor (familial hypercholesterolemia) COMMON PARC SNP DATA Chromosomal Location: 19p13.3 Gene-Specific Links: LocusLink (NCBI) GoldenPath (UCSC Genome Browser) PubMed Individual Genotypes Genotypes for each individual sample at each polymorphic site. 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

Injury Disease Nutrition Poison ... Prevention Familial hypercholesterolemia 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, 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. Individuals from families with a strong history of early heart attacks should be evaluated with a lipid screen. Proper diet, exercise, and the use of newer drugs can bring lipids down to safer levels.

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

Familial Hypercholesterolemia - FHC The pedigree to the right shows the inheritance of FHC over three generations. The affected gene which is located on chromosome 19 codes for the LDL receptor . The pedigree shows the following characteristics of an autosomal dominant mode of inheritance: direct transmission from an affected parent to an affected child (does not skip generations) transmission from affected male to affected male about a 1:1 ratio of affected:unaffected among progeny with one affected parent (7:5) Lecture on LDL (Univ. Illinois Chicago) This document maintained by Robert J. Huskey Last updated on July 1, 1996.

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

FAMILIAL HYPERCHOLESTEROLEMIA - A relatively rare (7 out of 1,000) genetic disease in which there is elevation in the blood triglycerides cholesterol , and low density lipoprotein LDL ). Also known as type II hyperlipoproteinemia familial hyperlipoproteinemia , or familial hypercholesterolemia Med Help International Library Search Ask the Doctor Forums The medical glossary has been made possible by a generous donation from:

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

HGM2003 Workshop Abstracts 2. Medical Genomics I Presentation 16 A Mexican kindred with familial hypercholesterolemia linked to chromosome 1p32 S. Canizales-Quinteros C. Aguilar-Salinas, E. Reyes-Rodriguez, L. Riba, S. Ramírez-Jiménez, M. Rodriguez-Torres, A. Huertas-Vázquez, V. Fragoso-Ontiveros, J. Rull, N.J. Cox, G.I. Bell, M.T. Tusié-Luna 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

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

Advanced Search Or click the first letter of a drug name: A B C D ... Z Browsing results for Homozygous Familial Hypercholesterolemia A B C D ... Z Drugs related to Homozygous Familial Hypercholesterolemia atorvastatin (consumer information) Crestor (consumer information) Lipitor (consumer information) rosuvastatin (consumer information) Home Drug Interactions Pill Identification Question.com ... About Drugs.com The drugs.com drug database is powered by Micromedex TM and Multum TM Micromedex data last updated 5 August 2005. Micromedex Physicians Desk Reference data last updated 18 July 2005. Multum data last updated 15 August 2005. We subscribe to the HONcode principles. Verify here Most Popular Drug Searches: Abilify Acetaminophen Aciphex Adderall ... Forum Drugs.com - prescription drug and medicine information available on over 24,000 approved- medications and pharmaceuticals, including side effects and drug interactions. Log-in Register Advertisement Buy a Link Now From our sponsors Categories Diabetes Gastro Center Weight Loss AIDS/HIV ... Sexual Health Advertisement Popular Searches Viagra Cialis Levitra Lipitor ... Pain Relief Advertisement

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

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. Articles Coronary Artery Disease in Heterozygous Familial Hypercholesterolemia Patients With the Same LDL Receptor Gene Mutation 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

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. Articles Coronary Artery Disease in Heterozygous Familial Hypercholesterolemia Patients With the Same LDL Receptor Gene Mutation 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. Abstract Top Abstract Introduction Methods Results Discussion References 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

Published online before print December 12, 2002, doi:10.1161/01.STR.0000047123.14312.3E Stroke A more recent version of this article appeared on January 1, 2003 This Article Full Text (PDF) Correction (v34,p826) All Versions of this Article: most recent 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 Lipids Peripheral vascular disease Genetics of cardiovascular disease ... Risk Factors for Stroke Submitted on July 18, 2002 Accepted on August 12, 2002 Risk of Fatal Stroke in Patients With Treated Familial Hypercholesterolemia. A Prospective Registry Study R. R. Huxley DPhil;

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

fax 525 4886 Fyrirlestrarskrá - Verkleg kennsla Verkefni Tilkynningar ... Tenglar Familial hypercholesterolemia Gen: : AD Spurningar Environemental modifiers Founder effects Gene dosage Genetic modifiers Helstu einkenni: Hypercholesterolemia Atherosclerosis Arcus senilis Xanthomas Myndin er eMedicine PubMed OMIM MedLinePlus eMedicine ... National heart, blood and lung Institute Verkefni: Umsj

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

fax 525 4886 Fyrirlestrarskrá - Verkleg kennsla Verkefni Tilkynningar ... Tenglar Familial hypercholesterolemia spurningar Spurningar: Heimild: Til baka Umsj

97. Familial Hypercholesterolemia (Disease) - Detroit, Michigan familial hypercholesterolemia (Disease) courtesy of Henry Ford Health Systemof Detroit, Michigan. http://www.henryfordhealth.org/14870.cfm

3D Tour of the Vattikuti Institute About the Institute The Vattikuti Institute Prostatectomy Prostate Cancer ... Related Content Related Content Familial hypercholesterolemia (Disease) Xanthoma - close-up Xanthoma - close-up Xanthoma on the knee 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. Individuals from families with a strong history of early heart attacks should be evaluated with a lipid screen. Proper diet, exercise, and the use of newer drugs can bring lipids down to safer levels.

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

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 Lipids Genetics of cardiovascular disease ACE/Angiotension receptors ... Risk Factors Hypertension. Scientific Contributions Renin-Angiotensin System Polymorphisms and Coronary Events in Familial Hypercholesterolemia Anthony S. Wierzbicki Michelle Lambert-Hammill Peter J. Lumb Martin A. Crook Abstract Top Abstract Introduction Methods Results Discussion References 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

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Clinical Chemistry 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. Articles Compound Heterozygous Familial Hypercholesterolemia and Familial Defective Apolipoprotein B-100 Produce Exaggerated Hypercholesterolemia E. Shyong Tai ,a Evelyn S.C. Koay Edmund Chan Tzer Jing Seng Lih Ming Loh Sunil K. Sethi and Chee Eng Tan Lipid Unit, Department of Endocrinology, Singapore General Hospital, Singapore 169608, Republic of Singapore. Department of Laboratory Medicine, National University Hospital, Singapore 119074, Republic of Singapore. Department of Pathology, National University of Singapore, Singapore 119260, Republic of Singapore.

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

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. ARTICLES Serum lipoprotein(a) in patients heterozygous for familial hypercholesterolemia, their relatives, and unrelated control populations 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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