Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli family

Keyphrases

• Israeli 100%
• Autosomal Dominant 100%
• Leukoencephalopathy 100%
• Subcortical Infarcts 100%
• Arteriopathy 100%
• NOTCH3 Gene 40%
• Chronic Disease 20%
• Jews 20%
• Monogenic 20%
• Lumbar Puncture 20%
• Ethnic Groups 20%
• Jewish Women 20%
• Clinical Phenotype 20%
• Smooth muscle Cells 20%
• Electron Microscopy 20%
• Computed Tomography 20%
• Genotype-phenotype 20%
• Small Media 20%
• Exon 20%
• Small-sized 20%
• T2-weighted Imaging (T2WI) 20%
• Basement Membrane 20%
• Molecular Analysis 20%
• Vascular Risk Factors 20%
• Amino Acid Substitution 20%
• Exon 4 20%
• Exon 3 20%
• Hypodensity 20%
• Granular Osmiophilic Material 20%
• Hyperintense Lesions 20%
• Medium-sized Vessel 20%
• Hemogram 20%
• Pericytes 20%
• Subcortical White Matter 20%
• Cerebral Angiography 20%
• Cranial Magnetic Resonance Imaging 20%
• Cranial Computed Tomography 20%
• Cerebral White Matter 20%

Medicine and Dentistry

• CADASIL Syndrome 100%
• Exon 40%
• Prevalence 20%
• Disease 20%
• Chronic Disease 20%
• Computer Assisted Tomography 20%
• Lumbar Puncture 20%
• Smooth Muscle Cell 20%
• Ethnic Group 20%
• Electron Microscopy 20%
• Intron 20%
• Basement Membrane 20%
• Amino Acid Substitution 20%
• Osmium 20%
• Microangiopathy 20%
• Magnetic Resonance Imaging of Head 20%
• Pericyte 20%