Spontaneous lobar haemorrhage in CADASIL[3]

Journal of Neurology, Neurosurgery and Psychiatry

Volumn 76, Issue 3, 2005, Pages 456-457

  MacLean, A V ^a   Woods, R ^a   Alderson, L M ^a   Salloway, S P ^a,b   Correia, S ^a   Cortez, S ^a   Stopa, E G ^a  

^a BROWN UNIVERSITY   (United States)

^b BUTLER HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BRAIN BIOPSY; BRAIN HEMORRHAGE; CADASIL; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; FRONTAL LOBE; GRAY MATTER; HUMAN; LETTER; MALE; MULTIPLE SCLEROSIS; PARIETAL LOBE; PRIORITY JOURNAL; WHITE MATTER;

CADASIL; CEREBRAL HEMORRHAGE; FRONTAL LOBE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; TOMOGRAPHY, X-RAY COMPUTED;

EID: 14544307386     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.2004.042564     Document Type: Letter

References (11)

1. Joutel A, Corpechot C, Ducros A, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 1996;383:707-10.
2. Dichgans M, Mayer M, Uttner I, et al. The phenotypic spectrum of CADASIL: clinical findings in 102 cases. Annals of Neurology 1998;44:731-9.
3. Ruchoux MM, Maurage CA. CADASIL: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencepholopathy. J Neuropathol Exp Neurol., 1997;56:947-64.
4. Lesnik Oberstein SA, van den Boom R, van Buchem MA, et al. Cerebral microbleeds in CADASIL. Neurology 2001;57.1066-70.
5. Sourander P, Walinder J. Hereditary multi-infarct dementia: morphological and clinical studies of a new disease. Acta Neuropathol (Berlin) 1977;39:247-54.
6. Kalimo H, Ruchoux MM, Viitanen M, et al. CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia. Brain Pathol 2002;12:371-84.
7. Baudrimont M, Dubas F, Joutel A, et al. Autosomal dominant leukoencephalopathy and subcortical ischemic stroke: a clinicopathological study. Stroke 1993;24:122-5.
8. Rouchoux MM, Maurage CA. Endothelial changes in muscle and skin biopsies in patients with CADASIL. Neuropathol Appl Neurobiol 1998;24:60-5.
9. Ruchoux MM, Domenga V, Brulin P, et al. Transgenic mice expressing mutant notch3 develop vascular alterations characteristic of cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy. Am J Pathol 2003;162:329-42.
10. Greenberg SM. Cerebral amyloid angiopathy and vessel dysfunction. Cerebrovasc Dis 2002;13(suppl 2):42-7.
11. Dichgans M, Holtmannspatter M, Herzog J, et al. Cerebral microbleeds in CADASIL: a gradient-echo magnetic resonance imaging and autopsy study. Stroke 2003;34:376-7.