Single-fiber EMG in familial hemiplegic migraine
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Abstract
Twelve familial hemiplegic migraine (FHM) patients (6 with the I1811L mutation in CACNA1A, 3 with M731T mutation in ATP1A2, and 3 without known mutations) and 10 control subjects underwent single-fiber EMG. Mean jitter did not differ significantly between patients and control subjects or among patients. No blocking was found. The results suggest that neuromuscular function is normal in FHM.
- Received December 5, 2003.
- Accepted July 9, 2004.
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- J. Gert van Dijk, Leiden University Medical Centre, PO Box 9600, 2300 RC Leiden, The Netherlandsj.g.van_dijk.neur@lumc.nl
- Gisela M Terwindt, Esther E. Kors, Alla A Vein, Michel D. Ferrari
Submitted January 21, 2005 - Single-fiber EMG in familial hemiplegic migraine
- Jean E Schoenen, University of Liège, University Department of Neurology.Headache Research Unit.CHR Citadelle.B-4000 Liège.Belgium.jschoenen@ulg.ac.be
- Anna Ambrosini, Alain Maertens de Noordhout
Submitted January 21, 2005
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