Common genetic mutations as possible aetiological factors in stroke

European Neurology

Volumn 45, Issue 2, 2001, Pages 119-120

  Szolnoki, Zoltán ^a,b   Somogyvári, Ferenc ^a   Szólics, Miklós ^a   Szabó, Mihaly ^a   Fodor, Lajos ^a  

^a Pandy Kalman County Hospital   (Hungary)

^b NONE   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN PROTEIN; HOMOCYSTEINE;

ADOLESCENT; ARTICLE; CASE REPORT; CEREBROVASCULAR ACCIDENT; CLINICAL EXAMINATION; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE COURSE; GENE MUTATION; GENETIC RISK; GENOTYPE; HUMAN; MALE; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM;

ADOLESCENT; FACTOR V; HETEROZYGOTE DETECTION; HUMANS; INTRACRANIAL EMBOLISM; MAGNETIC RESONANCE IMAGING; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MUTATION; OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; PEPTIDYL-DIPEPTIDASE A; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; THROMBOPHILIA; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0035106835     PISSN: 00143022     EISSN: None     Source Type: Journal    
DOI: 10.1159/000052105     Document Type: Article

References (18)

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8. C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: A case-control study
9. Methylenetetrahydrofolate reductase gene polymorphism: Relation to blood pressure cerebrovascular disease
10. Angiotensin-converting enzyme gene deletion polymorphism: A new risk factor for lacunet stroke but not carotid atheroma
11. Genetic susceptibility ischemic stroke
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13. World distribution of factor V Leiden
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17. Genetic and nongenetic factors influencing plasma homocysteine levels in patients with ischemic cerebrovascular disease and in healthy control subjects
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