Related references
Note: Only part of the references are listed.Staging and natural history of cerebrovascular pathology in dementia
V. Deramecourt et al.
NEUROLOGY (2012)
Pathogenesis of CADASIL Transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature
Anne Joutel
BIOESSAYS (2011)
Molecular genetics and pathology of hereditary small vessel diseases of the brain
Y. Yamamoto et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2011)
MRI Features of Pontine Autosomal Dominant Microangiopathy and Leukoencephalopathy (PADMAL)
Xiao-Qi Ding et al.
JOURNAL OF NEUROIMAGING (2010)
Neuropathological Correlates of Temporal Pole White Matter Hyperintensities in CADASIL
Yumi Yamamoto et al.
STROKE (2009)
C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
Anna Richards et al.
NATURE GENETICS (2007)
Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL
W. C. Low et al.
BRAIN (2007)
Arterioles of the lenticular nucleus in CADASIL
Qing Miao et al.
STROKE (2006)
Novel ophthalmological features in hereditary endotheliopathy with retinopathy, nephropathy and stroke syndrome
AC Cohn et al.
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY (2005)
Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL
C Hagel et al.
ACTA NEUROPATHOLOGICA (2004)
The pathogenesis of CADASIL: an update
RN Kalaria et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2004)
Towards defining the neuropathological substrates of vascular dementia
RN Kalaria et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2004)
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3
RA Ophoff et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Share Paper
