Results 141 to 150 of about 9,876 (239)

CADASIL Notch3 Mutant Proteins Localize to the Cell Surface and Bind Ligand

open access: bronze, 2002
Talin Haritunians   +8 more
openalex   +1 more source

Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL [PDF]

open access: bronze, 2006
Johanna Annunen‐Rasila   +8 more
openalex   +1 more source

CADASIL Registry in East Asia (CADREA): Protocol for an international prospective cohort study

open access: yesCerebral Circulation - Cognition and Behavior
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]

open access: green, 2007
Vincenzo Parisi   +8 more
openalex   +1 more source

CADASIL and cavernomas: A common mechanism

open access: yesAnnals of Indian Academy of Neurology, 2020
Ajay Garg   +5 more
openaire   +3 more sources

Myocardial Infarction in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)

open access: bronze, 2003
Saskia A.J. Lesnik Oberstein   +7 more
openalex   +1 more source

Mitochondrial Encephalopathy with CADASIL-Like MRI [PDF]

open access: green, 2007
Tamar Akhvlediani   +7 more
openalex   +1 more source

The protocol for an observational Australian cohort study of CADASIL: The AusCADASIL study

open access: yesCerebral Circulation - Cognition and Behavior
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  

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