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Volumn 31, Issue 6, 2011, Pages 760-762

Migraine attributed to genetic disorder: Proposal of a new category

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT MIGRAIN WITH VISUAL AURA; AUTOSOMAL DOMINANT RETINAL VASCULOPATHY WITH CEREBRAL LEUKODYSTROPHY; BASILAR TYPE MIGRAINE; CADASIL; CEREBROVASCULAR DISEASE; CHROMOSOME 10; EPILEPSY; FAMILIAL HEMIPLEGIC MIGRAINE; GENE MUTATION; GENETIC DISORDER; HEADACHE; HEREDITARY INFANTILE HEMIPARESIS, RETINAL ARTERIOLAR TORTUOSITY AND LEUCOENCEPHALOPATHY; HUMAN; LETTER; MELAS SYNDROME; MIGRAINE; MIGRAINE WITH AURA; MITOCHONDRIAL ENCEPHALOPATHY LACTIC ACIDOSIS AND STROKE LIKE EPISODE; NONHUMAN; SPORADIC HEMIPLEGIC MIGRAINE;

EID: 79954588919     PISSN: 03331024     EISSN: 14682982     Source Type: Journal    
DOI: 10.1177/0333102411398153     Document Type: Letter
Times cited : (4)

References (12)
  • 1
    • 74549161471 scopus 로고    scopus 로고
    • Proposals for new standardized general diagnostic criteria for the secondary headaches
    • Olesen J, Steiner T, Bousser M-G, Diener H-C, Dodick D, First MB, et al. Proposals for new standardized general diagnostic criteria for the secondary headaches. Cephalalgia. 2009 ; 29: 1331-1336
    • (2009) Cephalalgia , vol.29 , pp. 1331-1336
    • Olesen, J.1    Steiner, T.2    Bousser, M.-G.3    Diener, H.-C.4    Dodick, D.5    First, M.B.6
  • 2
    • 74549207436 scopus 로고    scopus 로고
    • The future of headache classification and classification research
    • Olesen J. The future of headache classification and classification research. Cephalalgia. 2009 ; 29: 1240-1241
    • (2009) Cephalalgia , vol.29 , pp. 1240-1241
    • Olesen, J.1
  • 3
    • 34547877951 scopus 로고    scopus 로고
    • Migraine attributed to genetic disorder
    • Sacco S, Carolei A. Migraine attributed to genetic disorder. Funct Neurol. 2007 ; 22: 117-118 (Pubitemid 47249618)
    • (2007) Functional Neurology , vol.22 , Issue.2 , pp. 117-118
    • Sacco, S.1    Carolei, A.2
  • 5
    • 77957280532 scopus 로고    scopus 로고
    • De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
    • Riant F, Ducros A, Ploton C, Barbance C, Depienne C, Tournier-Lasserve E. De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. Neurology. 2010 ; 75: 967-972
    • (2010) Neurology , vol.75 , pp. 967-972
    • Riant, F.1    Ducros, A.2    Ploton, C.3    Barbance, C.4    Depienne, C.5    Tournier-Lasserve, E.6
  • 7
    • 77957812064 scopus 로고    scopus 로고
    • A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura
    • Lafrenière RG, Cader MZ, Poulin JF, Andres-Enguix I, Simoneau M, Gupta N, et al. A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura. Nat Med. 2010 ; 16: 1157-1160
    • (2010) Nat Med , vol.16 , pp. 1157-1160
    • Lafrenière, R.G.1    Cader, M.Z.2    Poulin, J.F.3    Andres-Enguix, I.4    Simoneau, M.5    Gupta, N.6
  • 8
    • 77957287197 scopus 로고    scopus 로고
    • Diagnostic criteria for CADASIL in the International Classification of Headache Disorders (ICHD-II): Are they appropriate?
    • Sacco S, Degan D, Carolei A. Diagnostic criteria for CADASIL in the International Classification of Headache Disorders (ICHD-II): are they appropriate?. J Headache Pain. 2010 ; 11: 181-186
    • (2010) J Headache Pain , vol.11 , pp. 181-186
    • Sacco, S.1    Degan, D.2    Carolei, A.3
  • 9
    • 54949142139 scopus 로고    scopus 로고
    • Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: Basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome
    • Sproule DM, Kaufmann P. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome. Ann N Y Acad Sci. 2008 ; 1142: 133-158
    • (2008) Ann N y Acad Sci , vol.1142 , pp. 133-158
    • Sproule, D.M.1    Kaufmann, P.2
  • 11
    • 77955173802 scopus 로고    scopus 로고
    • COL4A1 mutations as a monogenic cause of cerebral small vessel disease. A systematic review
    • Lanfranconi S, Markus HS. COL4A1 mutations as a monogenic cause of cerebral small vessel disease. A systematic review. Stroke. 2010 ; 41: e513 - e518
    • (2010) Stroke , vol.41
    • Lanfranconi, S.1    Markus, H.S.2
  • 12
    • 1442265540 scopus 로고    scopus 로고
    • The international classification of headache disorders. 2nd ed
    • The international classification of headache disorders. 2nd ed. Cephalalgia. 2004 ; 24 (Suppl. 1). 9-160
    • (2004) Cephalalgia , vol.24 , Issue.SUPPL. 1 , pp. 9-160


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.