Sites of Interest which are a few of them, If you know of anymore, please e-mail info@cadasilfoundation.org Please see the links to websites on CADASIL. We are not responsible for any of the below links, they are only strictly of interest.
2009 links
NewsRx - CADASIL News Articles
http://searchmedica.com/xmlresource.do?c=pc&ss=defLink&p=Convera&rid=ds2-vb:p:2013t:82329600400:8c334e6463f737ce:4a62b67f&t=pubmed
2008 links
2007 links
Pregnancy following preimplantation genetic diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
2006
Characteristic features of in vivo skin microvascular reactivity in CADASIL
U-M Department of Neurology:Faculty
Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family
Small artery dementia in Japan: radiological differences between CADASIL, leukoaraiosis and Binswanger's disease.
CADASIL: a critical look at a Notch disease.
Changes in total cerebral blood flow and morphology in aging
Cadasil Project
Stroke research in China
CADASIL Exemplifies Small Vessel Disease of the Brain
Brain Stem and Cerebellar Hyperintense Lesions in Migraine
Ischemic demyelination.
Case report Psychosis or temporal lobotomy: SPECT findings in a paraplegic patient with chronic …
Structural MR Imaging Changes and Apolipoprotein E Genotype
Brief Communication Investigating the Association Between Notch3 Polymorphism and Migraine
Magnetic resonance imaging characteristics of CADASIL
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL
A chemical shift imaging study on regional metabolite distribution in a CADASIL family
Diffusion Tensor Imaging Study of Subcortical Gray Matter in CADASIL
CADASIL-causing mutations do not alter Notch3 receptor processing and activation
A novel cysteine-sparing Notch3 mutation
A new de novo Notch3 mutation causing CADASIL
Dilation of Virchow-Robin spaces in CADASIL
Characteristic features of in vivo skin microvascular reactivity in CADASIL.
The cognitive profiles of CADASIL and sporadic small vessel disease
CADASIL versus multiple sclerosis
Butler Hospital, Rhode Island
Critical look at a Notch disease
France CADASIL
Genetic disease appears to have three subtypes
Characteristic MR Lesion Pattern and Correlation of T1 and T2 Lesion
Clinical Presentation
Control of Tissue Patterning and Growth During Development
Genetic Condition Could Lead to Strokes During Pregnancy
National Organization of Rare Disease USA
Skin biopsy findings and results of neuropsychological testing in the first confirmed cases of CADASIL in Norway
Skin biopsy findings in CADASIL
Topic CADASIL
UK CADASIL Trust England
United Leukodystrophy Foundation
Blood pressure and haemoglobin A1c are associated with microhaemorrhage in CADASIL: a two-centre cohort study.
Two novel mutations in the NOTCH3 gene in Chinese.
Who is at Risk for Stroke?
2005
Peripheral neuropathy in CADASIL.
Is inadequate family history a barrier to diagnosis in CADASIL?
Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy
The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis.
Neurologic symptoms are common during gestation and puerperium in CADASIL.
CADASIL mutations impair Notch3 glycosylation by Fringe ...
Early visual function impairment in CADASIL.
Mayo Clinic Proceedings
Typical pathological changes of CADASIL in the optic nerve.
Stroke-21) Genetic Risk Factors
CADASIL: A Critical Look at a Notch Disease
Cerebellar arteriovenous malformation and vertebral artery aneurysm in a CADASIL patient
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephaloapthy (CADASIL): a hereditary cerebrovascular disease, which can be diagnosed by skin biopsy electron microscopy.
Disease Mutation Tracked Down, Ending ‘Curse’ for Colombian Families
Donepezil HCl in the Treatment of Subjects With Cognitive Impairment Associated CADASIL
An Animal Model for the Molecular Genetics of CADASIL
Behavioral analysis of transgenic animals
Mice carrying a R142C Notch 3 knock-in mutation do not develop a ...
Damage within a network of white matter regions underlies executive dysfunction in CADASIL
Functional analysis of a recurrent missense mutation in Notch3 in CADASIL
Large cerebral artery involvement in CADASIL
L-Arginine improves the symptoms of strokelike episodes in MELAS
Prognostic value of domain-specific cognitive abilities in acute first-ever stroke
Outline CADASIL
Neurologic symptoms are common during gestation and puerperium in CADASIL
Articles | Center of Flow Cytometry and FACS
Genetics Home Reference
2004
Bioline International Official Site (site up-dated regularly)
SGHMS: Clinical Neuroscience
Abnormal Vasoconstrictor Responses to Angiotensin II and Noradrenaline in Isolated small Arteries From Patients With CADASIL
A 52-year-old man with cognitive decline, seizure and stroke -- Simon et al. 170 (9): 1393 -- Canadian Medical
Histopathological abnormalities in ocular blood vessels of CADASIL patients.
Controlling hormones could reduce risk of strokes in younger people
Diffusion tensor imaging of thalamus correlates with cognition in CADASIL without dementia
Electrocardiogram in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Patients Without Any Clinical Evidence of Coronary Artery Disease. A Case-Control Study April 2006
Gene Review
Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy
Mice carrying a R142C Notch 3 knock-in mutation do not develop a CADASIL-like phenotype.
Influence of genetic and cardiovascular risk factors on the CADASIL phenotype
New Research Could Reduce Risk of Strokes in Younger People
2003
Early visual function impairment in CADASIL
Epidemiology and History
Cholinergic denervation in a pure multi-infarct state: Observations on CADASIL
Volume with Neurologic and Neuropsychological Findings in CADASIL
New differential diagnosis for vascular dementias
Coexistence of CADASIL and Alzheimer's disease -- Thijs et al. 74 (6): 790 -- Jour
Notch signaling and inherited disease syndromes -- Gridley 12 ...
"CADASIL coma": an underdiagnosed acute encephalopathy.
Avoid a Stroke, UAMS Experts Say
Transgenic Mice Expressing Mutant Notch3 Develop Vascular Alterations Characteristic CADASIL
Notch Signaling in Vascular Development
2002
Lessons from CADASIL
Diagnostic strategies in CADASIL
Mutated Notch 3 receptor exhibits impaired intracellular trafficking and maturation but normal ligand-induced signaling
Subcortical Lacunar Lesions: An MR Imaging Finding in Patients with CADASIL
A CADASIL-mutated Notch 3 receptor exhibits impaired intracellular trafficking and...
Cerebral Microbleeds in CADASIL: A Gradient-Echo Magnetic Resonance ...
Reversible coma with raised intracranial pressure: an unusual clinical manifestation of CADASIL
Lessons from CADASIL.
Vascular dementia: a diagnosis running out of time -- STEWART 180 (2): 152 -- The British Journal of Psychiatry
2001
Decrease in Regional Cerebral Blood Volume in Hyperintense Subcortical Lesions Inversely Correlates with Disability and Cognitive Performance
Differential Lesion Patterns in CADASIL and Sporadic Subcortical Arteriosclerotic Encephalopathy: MR Imaging Study with Statistical Parametric Group Comparison1
A magnetic resonance imaging study of the cervical cord of patients with CADASIL
CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.
Expression patterns of Notch1, Notch2, and Notch3 suggest multiple functional roles for the Notch-DSL signaling system during brain development.
Notch signaling during vascular development
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family
Cerebral microbleeds in CADASIL -- Lesnik Oberstein et al. 57 (6): 1066 -- Neurolo...
Vascular expression of Notch pathway receptors and ligands is restricted to arterial vessels
Nocturnal blood pressure dip in CADASIL
Notch signaling and inherited disease syndromes
NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL
No association between multiple sclerosis and the Notch3 gene responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
Altered white and gray matter metabolism in CADASIL
2000
Hereditary Vascular Dementia Linked to Notch 3 Mutations
Genetics and ischaemic stroke
CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): diagnostic skin biopsy changes determined by electron microscopy.
Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C content.
Notch signaling defect or protein accumulation problem?
Top of Form
Migraine with aura and white matter abnormalities: Notch3 mutation
Bottom of Form
Description of a simple test for CADASIL disease and determination of mutation frequencies in sporadic ischaemic stroke and dementia patients.
Vascular dementia today.
Analysis of HeyL expression in wild-type and Notch pathway mutant mouse embryos.
CADASIL: hereditary arteriopathy leading to multiple brain infarcts and dementia.
Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains
1999
Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL.
CADASIL: hereditary disease of arteries causing brain infarcts and dementia.
The natural history of CADASIL: a pooled analysis of previously published cases.
Young-adult-onset hereditary subcortical vascular dementia: cerebral autosomal recessive arteriosclerosis with subcortical infarcts and leukoencephalopathy (CARASIL)]
Clinical aspects, neuroradiology, genetics and diagnosis]
Brain stem MRI signal abnormalities in CADASIL.
Characteristic MR Lesion Pattern and Correlation of T1 and T2 Lesion Volume with Neurologic and Neuropsychological ...
1998
Leukoaraiosis and vascular dementia.
CADASIL syndrome: a genetic form of vascular dementia.
Notch signalling pathway and human diseases.
The phenotypic spectrum of CADASIL: clinical findings in 102 cases.
Epidemiology of vascular dementia.
Patterns of MRI lesions in CADASIL
differential diagnosis of a vascular leukoencephalopathy within a CADASIL family: use of skin biopsy electron microscopy study and direct genotypic screening
1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients.
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia
1996
CADASIL: skin biopsy allows diagnosis in early stages.
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine.
1995
Cadasil--a new model for subcortical dementia
Vascular dementia: a changing concept.
Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
1994
Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease.
Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]
1993
A gene for familial hemiplegic migraine maps to chromosome 19.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
Revised: October 25, 2009 info@cadasilfoundation.org All rights reserved. Copyright © 2009
