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25 results
  1. ... Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients Not a relevant reference standard Nakajima (2017) Differentiation of dementia with Lewy ...
  2. ... may contain more recent information. — ED. Table A. CADASIL: Genes and ... are compiled from the following standard references: gene from HGNC ; chromosome locus from OMIM ; protein ...
  3. People with dementia have serious problems with two or more brain functions, such as memory and language. Affects the ability to do normal activities. ...
  4. ... probability to moderate decrease) 5.1.4.11. CADASIL versus CADASIL-like syndromes 5.1.4.11.1. Results ... the evidence on rarer dementia subtypes (HAND, neurosyphilis, CADASIL, and corticobasal degeneration) was not sufficiently strong for ...
  5. ... and Justo Garcia (2009) On the diagnosis of CADASIL. Journal of Alzheimer’s disease: JAD 17(4), ... 2018 Jun. (NICE Guideline, No. 97.) Appendix I, References. PDF version of this page (664K) PDF version ...
  6. ... et al 2015 ]. Brain MRI resembling that of CADASIL ( c erebral a utosomal d ominant a rteriopathy ... and external capsule, which are characteristic signs in CADASIL, are also observed in early stages of CARASIL. ...
  7. ... Verbeek et al 2012 , Gunda et al 2014 ]. CADASIL ( c erebral a utosomal d ominant a rteriopathy ... subcortical infarcts on neuroimaging. The pathologic hallmark of CADASIL is electron-dense granules in the media of ...
  8. ... cortic*” or arterisclerotic) adj4 (encephalopath* or leukoencephalopath*)) or cadasil*).tw. 8 ((kosaka adj2 shibayama) or (neurofibrillary adj1 ... adj4 (Central adj4 nervous adj4 System)).tw. 65 (CADASIL or (cerebral adj4 autosomal adj4 dominant adj4 arteriopath* ...
  9. ... the possibility of inherited disorders such as MELAS , CADASIL , or thrombophilia (e.g., factor V Leiden ). Additional ... impairment, peripheral neuropathy, learning disability, & short stature NOTCH3 CADASIL AD Migraine may be 1st symptom; occurs in ...
  10. ... Disorders View in own window Disorder MOI Comment CADASIL AD NOTCH3 pathogenic variants are detected in exons 2-24 in persons w/CADASIL. The majority of sequence alterations are missense variants, ...
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