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Volumn 20, Issue 5, 2013, Pages 860-862
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Association of Chr17q25 with cerebral white matter hyperintensities and cognitive impairment: The J-SHIPP study
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Author keywords
Cognitive impairment; Genotype; White matter hyperintensity
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Indexed keywords
AGED;
ARTICLE;
BRAIN HEMORRHAGE;
CAROTID ATHEROSCLEROSIS;
CENTRAL NERVOUS SYSTEM DISEASE;
CEREBROVASCULAR DISEASE;
CHROMOSOME 17Q;
COGNITIVE DEFECT;
DEEP AND SUBCORTICAL WHITE MATTER HYPERINTENSITY;
GENETIC ASSOCIATION;
GENETIC POLYMORPHISM;
GENOTYPE;
HUMAN;
JAPANESE;
LACUNAR STROKE;
MAJOR CLINICAL STUDY;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PERIVENTRICULAR HYPERINTENSITY;
PRIORITY JOURNAL;
AGED;
ASIAN CONTINENTAL ANCESTRY GROUP;
CEREBROVASCULAR DISORDERS;
CHROMOSOMES, HUMAN, PAIR 17;
COGNITION DISORDERS;
FEMALE;
HUMANS;
MALE;
NERVE FIBERS, MYELINATED;
NEUROIMAGING;
POLYMORPHISM, SINGLE NUCLEOTIDE;
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EID: 84876325430
PISSN: 13515101
EISSN: 14681331
Source Type: Journal
DOI: 10.1111/j.1468-1331.2012.03879.x Document Type: Article |
Times cited : (17)
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References (4)
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