Submit a Response to This Article
Jump to comment:
No eLetters have been published for this article.
In this issue
Jump to section
Related Articles
Cited By...
- NOTCH3 variants are more common than expected in the general population and associated with stroke and vascular dementia: an analysis of 200 000 participants
- Novel Cysteine-Sparing Hypomorphic NOTCH3 A1604T Mutation Observed in a Family With Migraine and White Matter Lesions
- NOTCH3 variants are common in the general population and associated with stroke and vascular dementia: an analysis of 200,000 participants
- Features of Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts and Leukoencephalopathy
- Decreased T1 Contrast between Gray Matter and Normal-Appearing White Matter in CADASIL
- Extensive White Matter Hyperintensities May Increase Brain Volume in Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy
- The Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale: A Screening Tool to Select Patients for NOTCH3 Gene Analysis
- NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL
- Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients
- Neuropathological Correlates of Temporal Pole White Matter Hyperintensities in CADASIL
- Structural and metabolic brain abnormalities in preclinical cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy
- CADASIL: a guide to a comparatively unrecognised condition in psychiatry
- Heritability of MRI Lesion Volume in CADASIL: Evidence for Genetic Modifiers
- Review: magnetic resonance imaging alone is of limited usefulness in diagnosing multiple sclerosis