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Sites of Interest
We need volunteers to look up items for 2008 links!

2008 links

Aspirin-associated intracerebral hemorrhage in a patient with CADASIL
Hereditary Systemic Angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy, and hepatopathy
Diagnostic Criteria of Vascular Dementia in CADASIL

  

2007 links

Neuromusular implications in CADASIL.
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
Small cerebral vessel disease in familial amyloaid and non-amyloid angiopathies: FAD-PS-1 (P117L) mutation and CADASIL. Immunohistochemical and ultrastructural studies.
Brain atrophy is related to lacunar lesions and tissue microstructural changes in CADASIL.
The archetypal R90C CADASIL–NOTCH3 mutation retains NOTCH3 function in vivo
Proteome Analysis of Cultivated Vascular Smooth Meusccle Cells from a CADASIL Patient.
Reduction of optic nerve fiber layer thickness in CADASIL
Impaired Endothelial Function of Forearm Resistance Arteries in CADASIL Patients
Neuromuscular Implications in CADASIL
Lacunar Infarcts Are the Main Correlate With Cognitive Dysfunction in CADASIL
Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL.
Primary Prevention of Ischemic Stroke: A Guideline From the American 
15th European Stroke Conference
A/Professor Sally Dunwoodie - Victor Chang Cardiac Research Institute ...
AG Neurogenetik (LMU München) | CADASIL - Molecular and Cellular ...
Alzheimer Disease Overview
An unusual cause of stroke
Arkansas Blue Cross and Blue Shield
Brain Atrophy Is Related to Lacunar Lesions and Tissue Microstructural ...
CADASIL
CADASIL: what component of the vessel wall is really a target for Notch ...
cervical vascular disorder
Cognitive profile in CADASIL.
Dementia and Geriatric Cognitive Disorders
Dementia: Hope Through Research: National Institute of Neurological ...
DNA Tests (Description)
Genetics and dementia
Health News: Lifeclinic.com
Heritability of MRI lesion volume in CADASIL: evidence for genetic ...
http://www.galenicom.com/en/medline/article/16643314/au:Matthes+G
Magnetic Resonance Spectroscopy in CADASIL
NEJM -- Silent Brain Infarcts and the Risk of Dementia and Cognitive ...
Selected publications of Nicolas Molko
The cognitive profiles of CADASIL and sporadic small vessel disease.
The influence of genetic and cardiovascular risk factors on the ...
Systemic Blood Pressure Profile in Cerebral Autosomal Dominant ...

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

Impaired L-arginine induced vasoreactivity suggests endothelial dysfunction in CADASIL

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

Genetic Condition Could Lead to Strokes During Pregnancy

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.