CADASIL
"Questions about cadasil". www.cambridgestroke.com. Sencen, Lisa. "CADASIL". "CADASIL - About the Disease - Genetic and Rare ... A case of CADASIL presenting as schizophreniform organic psychosis has been reported. The underlying pathology of CADASIL is ... CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and ... Wikimedia Commons has media related to CADASIL syndrome. Lesnik Oberstein SA, Boon EM, Terwindt GM (June 28, 2012). CADASIL. ...
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
"CADASIL-CARASIL". www.cedars-sinai.edu. Retrieved 2019-11-05. Menezes Cordeiro Inês; Nzwalo Hipólito; Sá Francisca; Ferreira ... CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) "CARASIL". NORD (National ... Several disease that are frequently used for differential diagnoses include Binswanger's disease, CADASIL, Nasu-Hakula disease ... "CADASIL and CARASIL". Brain Pathology. 24 (5): 525-544. doi:10.1111/bpa.12181. hdl:10138/208443. ISSN 1750-3639. PMC 8029192. ...
Anne Joutel
Cadasil. The Lancet Neurology 8 (7), 643-653. (961 citations) E Tournier-Lasserve, A Joutel, J Melki, J Weissenbach, GM Lathrop ... Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 383 (6602), 707-710. (2103 ... She has a long-standing interest in CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and ... Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients. 1997. The Lancet 350 (9090), 1511-1515. (683 ...
Marie-Germaine Bousser
Bousser is most well known for her role in the discovery of CADASIL, a hereditary form of stroke. She researched the, then ... She won the Brain Prize in 2019 for her work on CADASIL. Bousser graduated from Paris-Sorbonne University in neuro-psychiatry ... They subsequently named the condition CADASIL. Bousser is Commander of the Legion of Honor (2013) and Grand Officer of the ...
Perivascular space
CADASIL syndrome (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome) is a ... Dilation is also a common characteristic of diseases or disorders of vascular pathologies, including CADASIL (cerebral ... "Dilation of Virchow-Robin spaces in CADASIL". European Journal of Neurology. 13 (2): 187-190. doi:10.1111/j.1468-1331.2006. ... an increased number of dilated spaces is observed in individuals with CADASIL. These perivascular spaces are localized ...
Proteinopathy
Spinner NB (March 2000). "CADASIL: Notch signaling defect or protein accumulation problem?". The Journal of Clinical ...
NOTCH3
Dichgans M, Herzog J, Gasser T (2001). "NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL". ... Joutel A, Tournier-Lasserve E (2002). "[Molecular basis and physiopathogenic mechanisms of CADASIL: a model of small vessel ... CADASIL). Mutations in NOTCH3 have also been identified in families with Alzheimer's disease. Adult Notch3 knock-out mice show ... "Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia". Nature. 383 (6602): 707-10. ...
Leukoencephalopathy
For example CADASIL syndrome is at the same time hereditary and hypoxic. Lyon, G.; Fattal-Valevski, A.; Kolodny, E. H. (2006 ...
Acetolactate synthase
No mutation was detected on this gene in CADASIL patients, suggesting that it is not implicated in this disorder. In the study ... CADASIL, an identified autosomal dominant condition characterized by the recurrence of subcortical infarcts leading to dementia ... "A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical region". Genomics. 38 (2): 192-8. doi ...
Autosomal dominant porencephaly type I
CADASIL syndrome is caused by a mutation in a different gene, but may cause similar symptoms. Sporadic porencephaly is another ...
Cerebrovascular disease
CADASIL is an inherited disorder caused by mutations in the NOTCH3 gene located on chromosome 19. NOTCH3 codes for a ... Examples of congenital cerebrovascular diseases include arteriovenous malformations, germinal matrix hemorrhage, and CADASIL ( ... including those that are congenital or idiopathic and include CADASIL, aneurysms, amyloid angiopathy, arteriovenous ...
Friedrich Nietzsche
Trimble postulated frontotemporal dementia while other researchers have proposed a hereditary stroke disorder called CADASIL. ...
Delta-like 1
Karlström H, Beatus P, Dannaeus K, Chapman G, Lendahl U, Lundkvist J (2003). "A CADASIL-mutated Notch 3 receptor exhibits ...
Migraine
Another genetic disorder associated with migraine is CADASIL syndrome or cerebral autosomal dominant arteriopathy with ...
Genetics of migraine headaches
Another genetic disorder associated with migraine is CADASIL syndrome or cerebral autosomal dominant arteriopathy with ...
The Luvvers
James Dewar, having found success as a member of the Robin Trower Band, died in 2002 from Cadasil hereditary stroke disorder. ...
Leukoencephalopathy with vanishing white matter
The Stennis Foundation CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) ...
Binswanger's disease
There are many diseases similar to Binswanger's disease including CADASIL syndrome and Alzheimer's disease, which makes this ...
Night in paintings (Western art)
It has been suggested John Ruskin had had CADASIL and the visual disturbances this condition caused him might have been a ...
Nocturne in Black and Gold - The Falling Rocket
It has been suggested John Ruskin suffered from CADASIL syndrome and the visual disturbances this condition caused him might ...
List of skin conditions
CADASIL syndrome) Cerebrotendinous xanthomatosis Citrullinemia Congenital erythropoietic porphyria (Gunther's disease) Diabetic ...
Donepezil
CADASIL syndrome, and Down syndrome. A three-year National Institutes of Health trial in people with mild cognitive impairment ...
List of syndromes
... syndrome Burnside-Butler syndrome Buschke-Ollendorff syndrome Bálint's syndrome Börjeson-Forssman-Lehmann syndrome CADASIL ...
Ankyrin repeat
... which can cause the neurological disorder CADASIL when the repeat domain is disrupted by mutations. A specialized family of ...
The Sea Inside
The film explores Ramón's relationships with two women: Julia, a lawyer suffering from Cadasil syndrome who supports his cause ...
Chromosome 19
Alternating hemiplegia of childhood Alzheimer's disease CADASIL Centronuclear myopathy autosomal dominant form Charcot-Marie- ...
List of MeSH codes (C10)
... cadasil MeSH C10.228.140.300.400.408 - dementia, multi-infarct MeSH C10.228.140.300.451 - hypoxia-ischemia, brain MeSH C10.228. ... cadasil MeSH C10.228.140.300.510.200.200 - cerebral amyloid angiopathy MeSH C10.228.140.300.510.200.200.160 - cerebral amyloid ...
Familial hemiplegic migraine
... are used to look for signs of other familial conditions such as CADASIL or mitochondrial disease, and for evidence of ...
Aura (symptom)
Neurological condition involving the crossing of senses CADASIL - autosomal dominant cerebrovascular disorder characterized by ...
Stroke in China
CADASIL), neural stem cell and stroke, neuroprotective treatment for stroke, clinical therapy test in stroke, rehabilitation ...