Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a Greek family

Neurological Sciences

Volumn 26, Issue 4, 2005, Pages 278-281

  Mandellos, D ^a   Limbitaki, G ^b   Papadimitriou, A ^b   Anastasopoulos, D ^a,b  

^a UNIVERSITY OF ATHENS   (Greece)

^b HENRY DUNANT HOSPITAL   (Greece)

Author keywords

CADASIL; Greek; Leiden; MTHFR; Mutation

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ACENOCOUMAROL; ANTICOAGULANT AGENT; ANTITHROMBIN III; ARGININE; BLOOD CLOTTING FACTOR 5 LEIDEN; CYSTEINE; NOTCH3 RECEPTOR;

ADULT; ARTICLE; BLOOD LEVEL; BRAIN HEMORRHAGE; CADASIL; CLINICAL ARTICLE; COMORBIDITY; CONTROLLED STUDY; EXON; FAMILIAL DISEASE; FATALITY; FEMALE; GENE MUTATION; GREECE; HETEROZYGOTE; HUMAN; MALE; RECURRENT DISEASE; RISK ASSESSMENT; STROKE; THROMBOPHILIA; THROMBOSIS;

ADULT; CADASIL; CEREBRAL INFARCTION; CEREBROVASCULAR ACCIDENT; FEMALE; GREECE; HUMANS; MALE; MIDDLE AGED; NUCLEAR FAMILY; PEDIGREE;

EID: 26844575183     PISSN: 15901874     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10072-005-0472-z     Document Type: Article

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