메뉴 건너뛰기




Volumn 30, Issue 2, 2008, Pages 146-150

Autosomal dominant leukoencephalopathy with mild clinical symptoms due to cerebrovascular dysfunctions: A new disease entity?

Author keywords

Autosomal dominant inheritance; CADASIL; Leukoencephalopathy; Migraine; Vasogenic edema

Indexed keywords

ADULT; ANAMNESIS; ARTERY WALL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT LEUKOENCEPHALOPATHY; BLOOD BRAIN BARRIER; BRAIN BLOOD FLOW; BRAIN EDEMA; CADASIL; CASE REPORT; CEREBROVASCULAR DISEASE; CLINICAL FEATURE; DIAGNOSTIC IMAGING; DIFFUSION WEIGHTED IMAGING; FAMILY HISTORY; FEMALE; GENE MUTATION; HUMAN; LEUKOENCEPHALOPATHY; MALE; MEDICAL EXAMINATION; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; WHITE MATTER;

EID: 38749088290     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.braindev.2007.06.003     Document Type: Article
Times cited : (4)

References (13)
  • 1
    • 0034763032 scopus 로고    scopus 로고
    • Magnetic resonance in childhood white-matter disorders
    • Van der Knaap M.S. Magnetic resonance in childhood white-matter disorders. Dev Med Child Neurol 43 (2001) 705-712
    • (2001) Dev Med Child Neurol , vol.43 , pp. 705-712
    • Van der Knaap, M.S.1
  • 6
    • 1642268710 scopus 로고    scopus 로고
    • Neuroimaging in posterior reversible encephalopathy syndrome
    • Lamy C., Oppenheim C., Meder J.F., and Mas J.L. Neuroimaging in posterior reversible encephalopathy syndrome. J Neuroimaging 14 (2004) 89-96
    • (2004) J Neuroimaging , vol.14 , pp. 89-96
    • Lamy, C.1    Oppenheim, C.2    Meder, J.F.3    Mas, J.L.4
  • 7
    • 33947584872 scopus 로고    scopus 로고
    • MR spectroscopy and diffusion tensor imaging of the brain in congenital muscular dystrophy with merosin deficiency: metabolite level decreases, fractional anisotropy decreases, and apparent diffusion coefficient increases in the white matter
    • Sijens P.E., Fock J.M., Meiners L.C., Potze J.H., Irwan R., and Oudkerk M. MR spectroscopy and diffusion tensor imaging of the brain in congenital muscular dystrophy with merosin deficiency: metabolite level decreases, fractional anisotropy decreases, and apparent diffusion coefficient increases in the white matter. Brain Dev 29 (2007) 317-321
    • (2007) Brain Dev , vol.29 , pp. 317-321
    • Sijens, P.E.1    Fock, J.M.2    Meiners, L.C.3    Potze, J.H.4    Irwan, R.5    Oudkerk, M.6
  • 8
    • 0035109913 scopus 로고    scopus 로고
    • Diffusion-weighted MR imaging in a case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
    • Yonemura K., Hasegawa Y., Kimura K., Minematsu K., and Yamaguchi T. Diffusion-weighted MR imaging in a case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. AJNR 22 (2001) 269-272
    • (2001) AJNR , vol.22 , pp. 269-272
    • Yonemura, K.1    Hasegawa, Y.2    Kimura, K.3    Minematsu, K.4    Yamaguchi, T.5
  • 9
    • 0028858163 scopus 로고
    • New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature
    • Verin M., Rolland Y., Landgraf F., Chabrit H., Bompais B., Michel A., et al. New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature. J Neurol Neurosurg Psychiatry 59 (1995) 579-585
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 579-585
    • Verin, M.1    Rolland, Y.2    Landgraf, F.3    Chabrit, H.4    Bompais, B.5    Michel, A.6
  • 10
    • 0036144290 scopus 로고    scopus 로고
    • Leukoaraiosis, ischemic stroke, and normal white matter on diffusion-weighted MRI
    • Helenius J., Soinne L., Salonen O., Kaste M., and Tatlisumak T. Leukoaraiosis, ischemic stroke, and normal white matter on diffusion-weighted MRI. Stroke 33 (2002) 45-50
    • (2002) Stroke , vol.33 , pp. 45-50
    • Helenius, J.1    Soinne, L.2    Salonen, O.3    Kaste, M.4    Tatlisumak, T.5
  • 13
    • 0038278343 scopus 로고    scopus 로고
    • Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of NOTCH3 mutations and implications of smooth muscle cell degeneration for the pathogenesis
    • Santa Y., Uyama E., Chui D.H., Arima M., Kotorii S., Takahashi K., et al. Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of NOTCH3 mutations and implications of smooth muscle cell degeneration for the pathogenesis. J Neurol Sci 212 (2003) 79-84
    • (2003) J Neurol Sci , vol.212 , pp. 79-84
    • Santa, Y.1    Uyama, E.2    Chui, D.H.3    Arima, M.4    Kotorii, S.5    Takahashi, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.