CADASIL Notch3 Mutant Proteins Localize to the Cell Surface and Bind Ligand
Talin Haritunians+8 more
openalex +1 more source
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL [PDF]
Johanna Annunen‐Rasila+8 more
openalex +1 more source
CADASIL Registry in East Asia (CADREA): Protocol for an international prospective cohort study
Introduction: Recent advancements in genomic research have revealed that 9 individuals per 1,000 population in East Asia and 3.4 individuals per 1,000 population worldwide carry cysteine-altering NOTCH3 variants in the epidermal growth factor-like repeat
Satoshi Saito+8 more
doaj
Reduction of optic nerve fiber layer thickness in CADASIL [PDF]
Vincenzo Parisi+8 more
openalex +1 more source
CADASIL and cavernomas: A common mechanism
Ajay Garg+5 more
openaire +3 more sources
Signaling pathways and molecular mechanisms involved in the onset and progression of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL); a focus on Notch3 signaling. [PDF]
Heidari P, Taghizadeh M, Vakili O.
europepmc +1 more source
Mitochondrial Encephalopathy with CADASIL-Like MRI [PDF]
Tamar Akhvlediani+7 more
openalex +1 more source
The protocol for an observational Australian cohort study of CADASIL: The AusCADASIL study
Introduction: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a rare genetic condition with a broad phenotypic presentation.
Danit G. Saks+33 more
doaj
The influence of genetic and cardiovascular risk factors on the CADASIL phenotype
Shailvi Singhal
openalex +1 more source