Fanconi anemia and moyamoya: Evidence for an association

Neurology

Volumn 45, Issue 5, 1995, Pages 998-1000

  Pavlakis, Steven G ^a   Verlander, P C ^b   Gould, R J ^a   Strimling, B C ^c   Auerbach, A D ^b  

^a WEILL CORNELL MEDICAL CENTER   (United States)

^b ROCKEFELLER UNIVERSITY   (United States)

^c Oregon Medical Group   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; HEMOGLOBIN; IMMUNOGLOBULIN; OXYMETHOLONE; PREDNISONE;

ACUTE FEBRILE NEUTROPHILIC DERMATOSIS; ANGIOGRAPHY; ARTICLE; CASE REPORT; CHILD; CHROMOSOME BREAKAGE; ERYTHROCYTE TRANSFUSION; FANCONI ANEMIA; FEMALE; GENE; GENE MUTATION; HUMAN; INTRAVENOUS DRUG ADMINISTRATION; MOYAMOYA DISEASE; PRIORITY JOURNAL; THROMBOCYTE TRANSFUSION;

CASE REPORT; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FANCONI ANEMIA; FEMALE; HUMAN; MOYAMOYA DISEASE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0029042362     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.45.5.998     Document Type: Article

References (10)

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