Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Latest Advances

Retinal Vessel Dysfunction in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: An Ultra-Widefield Fluorescein Angiography Study.

Journal: Neurology open access

Published: June 15, 2026

Cortical correlates of apathy in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy with two different pathogenic mutations in the NOTCH3 gene.

Journal: Neuropsychology

Published: June 15, 2026

The role of inflammation in cerebral small vessel disease and vascular cognitive impairment, and therapeutic implications.

Journal: International journal of stroke : official journal of the International Stroke Society

Published: June 08, 2026

Recognising CADASIL in adults with NPH-like syndrome.

Journal: BMJ case reports

Published: June 03, 2026

Comment on "Genetic testing for adult-onset neurodegenerative diseases: A clinical perspective".

Journal: Journal of the Formosan Medical Association = Taiwan yi zhi

Published: May 21, 2026

Novel Mutation of NOTCH3 Gene in a Chinese Patient with CADASIL.

Journal: Balkan journal of medical genetics : BJMG

Published: May 18, 2026

NOTCH3-R544C mutation drives endothelial dysfunction through inflammation, migration impairment, and lipid dysregulation.

Journal: Journal of Alzheimer's disease : JAD

Published: April 21, 2026

CADASIL: a practical review for the neurologist.

Journal: Practical neurology

Published: April 16, 2026

Age-dependent vascular and neurological characteristics of CADASIL are recapitulated in Notch3 mutant zebrafish, implicating a role for type IV collagen in disease progression.

Journal: Acta neuropathologica communications

Published: April 11, 2026

Determinants of cerebral microbleed presence and burden in CADASIL.

Journal: Cerebral circulation - cognition and behavior

Published: April 09, 2026

An in trans NOTCH3 loss-of-function variant modifies disease severity in CADASIL: A family-based study.

Journal: Journal of the Chinese Medical Association : JCMA

Published: April 08, 2026

Selective vulnerability of cerebral vasculature to NOTCH3 variants in small vessel disease and rescue by phosphodiesterase-5 inhibitor.

Journal: Science advances

Published: April 03, 2026

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Latest Advances

Find the Latest Research About Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Retinal Vessel Dysfunction in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: An Ultra-Widefield Fluorescein Angiography Study.

Retinal Vessel Dysfunction in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: An Ultra-Widefield Fluorescein Angiography Study.

Cortical correlates of apathy in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy with two different pathogenic mutations in the NOTCH3 gene.

Cortical correlates of apathy in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy with two different pathogenic mutations in the NOTCH3 gene.

The role of inflammation in cerebral small vessel disease and vascular cognitive impairment, and therapeutic implications.

The role of inflammation in cerebral small vessel disease and vascular cognitive impairment, and therapeutic implications.

Recognising CADASIL in adults with NPH-like syndrome.

Recognising CADASIL in adults with NPH-like syndrome.

Comment on "Genetic testing for adult-onset neurodegenerative diseases: A clinical perspective".

Comment on "Genetic testing for adult-onset neurodegenerative diseases: A clinical perspective".

Novel Mutation of NOTCH3 Gene in a Chinese Patient with CADASIL.

Novel Mutation of NOTCH3 Gene in a Chinese Patient with CADASIL.

NOTCH3-R544C mutation drives endothelial dysfunction through inflammation, migration impairment, and lipid dysregulation.

NOTCH3-R544C mutation drives endothelial dysfunction through inflammation, migration impairment, and lipid dysregulation.

CADASIL: a practical review for the neurologist.

CADASIL: a practical review for the neurologist.

Age-dependent vascular and neurological characteristics of CADASIL are recapitulated in Notch3 mutant zebrafish, implicating a role for type IV collagen in disease progression.

Age-dependent vascular and neurological characteristics of CADASIL are recapitulated in Notch3 mutant zebrafish, implicating a role for type IV collagen in disease progression.

Determinants of cerebral microbleed presence and burden in CADASIL.

Determinants of cerebral microbleed presence and burden in CADASIL.

An in trans NOTCH3 loss-of-function variant modifies disease severity in CADASIL: A family-based study.

An in trans NOTCH3 loss-of-function variant modifies disease severity in CADASIL: A family-based study.

Selective vulnerability of cerebral vasculature to NOTCH3 variants in small vessel disease and rescue by phosphodiesterase-5 inhibitor.

Selective vulnerability of cerebral vasculature to NOTCH3 variants in small vessel disease and rescue by phosphodiesterase-5 inhibitor.