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Volumn 52, Issue 1, 2010, Pages 103-104

Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: A novel de novo CACNA1A gene mutation

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CALCIUM CHANNEL; GLYCINE;

EID: 73249129712     PISSN: 00121622     EISSN: 14698749     Source Type: Journal    
DOI: 10.1111/j.1469-8749.2009.03493.x     Document Type: Letter
Times cited : (24)

References (11)
  • 1
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    • The international classification of headache disorders
    • The international classification of headache disorders. Cephalalgia 2004, 24:28-9.
    • (2004) Cephalalgia , vol.24 , pp. 28-29
  • 2
    • 33646270177 scopus 로고    scopus 로고
    • Sporadic and familial hemiplegic migraine: diagnosis and treatment
    • Black DF. Sporadic and familial hemiplegic migraine: diagnosis and treatment. Semin Neurol 2006, 26:208-16.
    • (2006) Semin Neurol , vol.26 , pp. 208-216
    • Black, D.F.1
  • 3
    • 9644287998 scopus 로고    scopus 로고
    • Sporadic hemiplegic migraine
    • Thomsen LL, Olesen J. Sporadic hemiplegic migraine. Cephalalgia 2004, 24:1016-23.
    • (2004) Cephalalgia , vol.24 , pp. 1016-1023
    • Thomsen, L.L.1    Olesen, J.2
  • 4
    • 0034633752 scopus 로고    scopus 로고
    • CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
    • Vahedi K, Denier C, Ducros A. CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy. Neurology 2000, 55:1040-2.
    • (2000) Neurology , vol.55 , pp. 1040-1042
    • Vahedi, K.1    Denier, C.2    Ducros, A.3
  • 6
    • 0033364409 scopus 로고    scopus 로고
    • Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
    • Ducros A, Denier C, Joutel A. Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia. Am J Hum Genet 1999, 64:89-98.
    • (1999) Am J Hum Genet , vol.64 , pp. 89-98
    • Ducros, A.1    Denier, C.2    Joutel, A.3
  • 7
    • 0036279411 scopus 로고    scopus 로고
    • Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine
    • Terwindt G, Kors E, Haan J. Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine. Arch Neurol 2002, 59:1016-8.
    • (2002) Arch Neurol , vol.59 , pp. 1016-1018
    • Terwindt, G.1    Kors, E.2    Haan, J.3
  • 8
    • 37349078332 scopus 로고    scopus 로고
    • Systemic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine
    • De Vries B, Freilinger T, Vanmolkot KRJ. Systemic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine. Neurology 2007, 69:2170-6.
    • (2007) Neurology , vol.69 , pp. 2170-2176
    • De Vries, B.1    Freilinger, T.2    Vanmolkot, K.R.J.3
  • 11
    • 0034988145 scopus 로고    scopus 로고
    • Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine
    • Kors EE, Terwindt GM, Vermeulen FL. Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Ann Neurol 2001, 49:753-60.
    • (2001) Ann Neurol , vol.49 , pp. 753-760
    • Kors, E.E.1    Terwindt, G.M.2    Vermeulen, F.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.