The McLeod syndrome without acanthocytes

Parkinsonism and Related Disorders

Volumn 14, Issue 4, 2008, Pages 364-366

  Klempíř, Jiří ^a   Roth, Jan ^a   Zárubová, Kateřina ^a   Písačka, Martin ^b   Špačková, Nataša ^a   Tilley, Louise ^c  

^a CHARLES UNIVERSITY   (Czech Republic)

^b INSTITUTE OF HEMATOLOGY AND BLOOD TRANSFUSION   (Czech Republic)

^c NHS BLOOD AND TRANSPLANT   (United Kingdom)

Author keywords

Acanthocytosis; Behavioural changes; Caudate atrophy; Chorea; McLeod syndrome

Indexed keywords

CREATINE KINASE; LACTATE DEHYDROGENASE; MEMBRANE PROTEIN; PROTEIN XK;

ACANTHOCYTOSIS; ADULT; ANTIGEN EXPRESSION; ARTICLE; BEHAVIOR CHANGE; BLOOD GROUP KELL SYSTEM; CASE REPORT; CAUSE OF DEATH; CHOREA; CREATINE KINASE BLOOD LEVEL; DELIRIUM; DISEASE SEVERITY; ERYTHROCYTE; GENE MUTATION; HEART ARRHYTHMIA; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; HYPOGLYCEMIA; KIDNEY FAILURE; LACTATE DEHYDROGENASE BLOOD LEVEL; LIVER FAILURE; MALE; MCLEOD SYNDROME; MUSCLE ATROPHY; POLYNEUROPATHY; PRIORITY JOURNAL; RHABDOMYOLYSIS;

ACANTHOCYTES; AMINO ACID TRANSPORT SYSTEMS, NEUTRAL; CHOREA; CREATINE KINASE; HUMANS; HYDRO-LYASES; KELL BLOOD-GROUP SYSTEM; MALE; MIDDLE AGED; MUTATION; SEX CHROMOSOME DISORDERS;

EID: 44249124738     PISSN: 13538020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2007.07.011     Document Type: Article

References (10)

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