A case of familial hemiplegic migraine associated with a novel atp1a2 gene mutation

Pediatric Neurology

Volumn 47, Issue 2, 2012, Pages 133-136

  De Cunto, Angela ^a   Bensa, Marco ^b   Tonelli, Alessandra ^c  

^a UNIVERSITY OF TRIESTE   (Italy)

^b BUFALINI HOSPITAL   (Italy)

^c SCIENTIFIC INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CATION TRANSPORT PROTEIN; DIMENHYDRINATE; FLUNARIZINE; SODIUM POTASSIUM ADENOSINE TRIPHOSPHATASE ALPHA 2; TRAMADOL; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME; ELECTROENCEPHALOGRAM; EXON; FAMILIAL HEMIPLEGIC MIGRAINE; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCHOOL CHILD; TREATMENT RESPONSE;

AMINO ACID SEQUENCE; CHILD, PRESCHOOL; HUMANS; MALE; MIGRAINE WITH AURA; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; SODIUM-POTASSIUM-EXCHANGING ATPASE;

EID: 84863326275     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2012.04.012     Document Type: Article

References (11)

1. A.A. Gelfand, H.J. Fullerton, and P.J. Goadsby Child neurology: Migraine with aura in children Neurology 75 2010 e16 e19
2. M.B. Russell, and A. Ducros Sporadic and familial hemiplegic migraine: Pathophysiological mechanisms, clinical characteristics, diagnosis, and management Lancet Neurol 10 2011 457 470
3. A. Ducros, C. Denier, and A. Joutel The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel N Engl J Med 345 2001 17 24
4. S.D. Wheeler Phenotype-driven preventive strategies for migraine and other headaches Neurologist 15 2009 59 70
5. B. Varkey, and L. Varkey EEG in hemiplegic migraine Neurol India 52 2004 134
6. D.J. Butteriss, V. Ramesh, and D. Birchall Serial MRI in a case of familial hemiplegic migraine Neuroradiology 45 2003 300 303
7. V. Artto, M. Nissilä, M. Wessman, A. Palotie, M. Färkkilä, and M. Kallela Treatment of hemiplegic migraine with triptans Eur J Neurol 14 2007 1053 1056
8. L.L. Thomsen, M. Kirchmann, and A. Bjornsson The genetic spectrum of a population-based sample of familial hemiplegic migraine Brain 130 2007 346 356
9. J.M. Hansen, L.L. Thomsen, J. Olesen, and M. Ashina Coexisting typical migraine in familial hemiplegic migraine Neurology 74 2010 594 600
10. F. Riant, M. De Fusco, and P. Aridon ATP1A2 mutations in 11 families with familial hemiplegic migraine Hum Mutat 26 2005 281
11. K.R. Vanmolkot, H. Stroink, and J.B. Koenderink Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation Ann Neurol 59 2006 310 314