Genetic risk factors for cerebrovascular disease in children with sickle cell disease: Design of a case-control association study and genomewide screen

BMC Medical Genetics

Volumn 4, Issue , 2003, Pages

  Adams, Gaye T ^a   Snieder, Harold ^a,b   McKie, Virgil C ^a   Clair, Betsy ^a   Brambilla, Donald ^c   Adams, Robert J ^a   Kutlar, Ferdane ^a   Kutlar, Abdullah ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

^b ST THOMAS HOSPITAL   (United Kingdom)

^c NEW ENGLAND RESEARCH INSTITUTES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ADENINE; APOLIPOPROTEIN A1; APOLIPOPROTEIN E; BETA GLOBIN; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; BLOOD CLOTTING FACTOR 8; DIPEPTIDYL CARBOXYPEPTIDASE; DNA; ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE 1; FIBRINOGEN; FIBRINOGEN RECEPTOR; GLUTAMIC ACID; GLYCOPROTEIN IB; INTERCELLULAR ADHESION MOLECULE 1; L SELECTIN; PADGEM PROTEIN; PLASMINOGEN ACTIVATOR INHIBITOR 1; PROTHROMBIN; THROMBOMODULIN; TUMOR NECROSIS FACTOR ALPHA; TYROSINE; VALINE; VASCULAR CELL ADHESION MOLECULE 1; VERY LATE ACTIVATION ANTIGEN 2;

ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; BLOOD FLOW VELOCITY; BLOOD VESSEL REACTIVITY; BRAIN BLOOD FLOW; CASE CONTROL STUDY; CELL ADHESION; CELL FUNCTION; CEREBROVASCULAR ACCIDENT; CEREBROVASCULAR DISEASE; CHILD; CONTROLLED STUDY; DNA DETERMINATION; DOPPLER ECHOGRAPHY; ENDOTHELIUM CELL; GENE FUNCTION; GENE INTERACTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC SCREENING; GENOTYPE; HEREDITY; HIGH RISK PATIENT; HUMAN; HUMAN CELL; INFLAMMATION; LIPID METABOLISM; MAJOR CLINICAL STUDY; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; METHODOLOGY; PATHOGENESIS; PHENOTYPE; RISK FACTOR; SICKLE CELL ANEMIA; SINGLE NUCLEOTIDE POLYMORPHISM; THROMBOCYTE ACTIVATION; THROMBOCYTE FUNCTION;

ADOLESCENT; AFRICAN AMERICANS; ANEMIA, SICKLE CELL; CASE-CONTROL STUDIES; CEREBROVASCULAR DISORDERS; CHILD; CHILD, PRESCHOOL; DNA; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOME, HUMAN; HUMANS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RANDOM ALLOCATION; RISK FACTORS; ULTRASONOGRAPHY, DOPPLER, TRANSCRANIAL;

EID: 2542470807     PISSN: 14712350     EISSN: None     Source Type: Journal    
DOI: 10.1186/1471-2350-4-6     Document Type: Article

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