Recurrent stroke due to a novel voltage sensor mutation in cav2.1 responds to verapamil

Stroke

Volumn 42, Issue 2, 2011, Pages

  Knierim, Ellen ^a   Leisle, Lilia ^b   Wagner, Christiane ^a   Weschke, Bernhard ^a   Lucke, Barbara ^a   Bohner, Georg ^a   Dreier, Jens P ^a   Schuelke, Markus ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

Author keywords

calcium channels; genetics; pediatric neurology; pediatric stroke; stroke in children

Indexed keywords

ARGININE; VERAPAMIL;

ARTICLE; CALCIUM TRANSPORT; CASE REPORT; CHILD; CLINICAL FEATURE; CONSCIOUSNESS DISORDER; DIGITAL SUBTRACTION ANGIOGRAPHY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HEAD INJURY; HEMIPARESIS; HUMAN; PRIORITY JOURNAL; RECURRENT DISEASE; SEIZURE; SEQUENCE ANALYSIS; STROKE;

CALCIUM CHANNELS; CALCIUM CHANNELS, N-TYPE; CHILD; FEMALE; HUMANS; MUTATION; RECURRENCE; STROKE; VERAPAMIL;

EID: 79251624176     PISSN: 00392499     EISSN: None     Source Type: Journal    
DOI: 10.1161/STROKEAHA.110.600023     Document Type: Article

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