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Volumn 63, Issue 10, 2004, Pages 1942-1943

Single-fiber EMG in familial hemiplegic migraine

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL P TYPE; CALCIUM CHANNEL Q TYPE;

EID: 8844221146     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000144342.35011.54     Document Type: Article
Times cited : (21)

References (10)
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  • 2
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    • Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
    • Ophoff RA, Terwindt GM, Vergouwe MN, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 1996;87:543-552.
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  • 3
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    • Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
    • Terwindt GM, Ophoff RA, van Eijk R, et al. Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura. Neurology 2001;56:1028-1032.
    • (2001) Neurology , vol.56 , pp. 1028-1032
    • Terwindt, G.M.1    Ophoff, R.A.2    Van Eijk, R.3
  • 4
    • 0037312922 scopus 로고    scopus 로고
    • Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2
    • De Fusco M, Marconi R, Silvestri L, et al. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet 2003;33:192-196.
    • (2003) Nat Genet , vol.33 , pp. 192-196
    • De Fusco, M.1    Marconi, R.2    Silvestri, L.3
  • 5
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    • Novel mutations in the Na⊥, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
    • Vanmolkot KR, Kors EE, Hottenga JJ, et al. Novel mutations in the Na⊥, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Ann Neurol 2003;54:360-366.
    • (2003) Ann Neurol , vol.54 , pp. 360-366
    • Vanmolkot, K.R.1    Kors, E.E.2    Hottenga, J.J.3
  • 6
    • 0033981451 scopus 로고    scopus 로고
    • Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha (1A) Ca (2+) channel mutation
    • Plomp JJ, Vergouwe MN, Van den Maagdenberg AM, Ferrari MD, Frants RR, Molenaar PC. Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha (1A) Ca (2+) channel mutation. Brain 2000;123:463-471.
    • (2000) Brain , vol.123 , pp. 463-471
    • Plomp, J.J.1    Vergouwe, M.N.2    Van Den Maagdenberg, A.M.3    Ferrari, M.D.4    Frants, R.R.5    Molenaar, P.C.6
  • 7
    • 0035942346 scopus 로고    scopus 로고
    • Neuromuscular transmission in migraine. A single-fiber EMG study in clinical subgroups
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    • (2001) Neurology , vol.56 , pp. 1038-1043
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  • 8
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    • Acetazolamide acts on neuromuscular transmission abnormalities found in some migraineurs
    • Ambrosini A, Pierelli F, Schoenen. Acetazolamide acts on neuromuscular transmission abnormalities found in some migraineurs. Cephalgia 2003;23:75-78.
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    • Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.