• <em>NOTCH3</em> Variants in Patients with Suspected CADASIL
• A Case Report of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Misdiagnosed as Multiple Sclerosis
• A multicenter, single-arm, phase II clinical trial of adrenomedullin in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
• A Search for New Biological Pathways in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy by Proteomic Research
• Age-related loss of Notch3 underlies brain vascular contractility deficiencies, glymphatic dysfunction, and neurodegeneration in mice
• Alzheimer's disease with a CADASIL twist - neuropathological examination proves its value in clarifying the genetics behind familial dementia
• Association of NOTCH3 Variant Risk Category With 2-Year Clinical and Radiologic Small Vessel Disease Progression in Patients With CADASIL
• Associations between neurovascular coupling and cerebral small vessel disease: A systematic review and meta-analysis
• Autosomal Recessive NOTCH3-Related Leukodystrophy in Two Siblings and Review of the Literature
• BACE1 and SCD1 are associated with neurodegeneration
• Bilateral non-arteritic anterior ischemic optic neuropathy as first manifestation of CADASIL in an elderly patient
• Blood vessel organoids generated by base editing and harboring single nucleotide variation in Notch3 effectively recapitulate CADASIL-related pathogenesis
• Border zone cerebral infarcts associated with COVID-19 in CADASIL : a report of 3 cases and literature review
• Border-Zone Cerebral Infarcts Associated with COVID-19 in CADASIL: A Report of 3 Cases and Literature Review
• Broadening the Genetic Horizons of CADASIL: New Variants of the NOTCH3 Gene Revealed and their Association with CADASIL
• CADASIL Type 2 (HTRA1 Cerebral Small Vessel Disease) in an Indian Woman
• CADASIL: A NOTCH3-associated cerebral small vessel disease
• Cerebral Autosomal Dominant Arteriopathy
• Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) in a 25-Year-Old Patient: A Case Report
• Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Syndrome: A Case Report and Review of Literature
• Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with multiple different onset forms of frequent recurrent attacks: A case report and literature review
• Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL): A Diagnosis to Consider in Atypical Stroke Presentations
• Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy presenting as recurrent stroke and ataxia
• Chorea Associated with Genetic-Confirmed CADASIL
• Chorea Associated with Notch3 Gene Mutation
• Clinical and neuroimaging review of monogenic cerebral small vessel disease from the prenatal to adolescent developmental stage
• Comparison of models for stroke-free survival prediction in patients with CADASIL
• Contribution of the <em>APOE</em> Genotype to Cognitive Impairment in Individuals With <em>NOTCH3</em> Cysteine-Altering Variants
• Correction to: Modeling CADASIL vascular pathologies with patient-derived induced pluripotent stem cells
• Correction: Szymanowicz et al. Headache and NOTCH3 Gene Variants in Patients with CADASIL. Neurol. Int. 2023, 15, 1238-1252
• Corrigendum: A heterozygous mutation in <em>NOTCH3</em> in a Chinese family with CADASIL
• Corrigendum: A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL
• Cortical type memory impairment in CADASIL: Watch out for the second train!
• Cysteine-Altering NOTCH3 Variants Are Associated with an Increased Risk of Autoimmune Diseases
• Decreased retinal vascular density is associated with cognitive impairment in CADASIL: an optical coherence tomography angiography study
• Deep learning based on susceptibility-weighted MR sequence for detecting cerebral microbleeds and classifying cerebral small vessel disease
• Dental procedure induced cerebellar haemorrhage with visual tilt and unsuspected CADASIL
• Detecting a Novel NOTCH3 Variant in Patients with Suspected CADASIL: A Single Center Study
• Development and validation of a two-stage convolutional neural network algorithm for segmentation of MRI white matter hyperintensities for longitudinal studies in CADASIL
• Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritance
• Early remodeling and loss of light-induced dilation of retinal small arteries in CADASIL
• Effect of blood pressure-lowering agents on microvascular function in people with small vessel diseases (TREAT-SVDs): a multicentre, open-label, randomised, crossover trial
• Effect of corticosubcortical iron deposition on dysfunction in CADASIL is mediated by white matter microstructural damage
• Enlarged perivascular spaces are associated with white matter injury, cognition and inflammation in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
• Expanding the Neurological Phenotype of Anderson-Fabry Disease: Proof of Concept for an Extrapyramidal Neurodegenerative Pattern and Comparison with Monogenic Vascular Parkinsonism
• First intravenous thrombolysis for pCys194Arg Notch 3 mutation in a Moroccan CADASIL patient with stroke
• First report of a p.Cys484Tyr Notch3 mutation in a CADASIL patient with acute bilateral multiple subcortical infarcts-case report and brief review
• Four Novel Disease-Causing Variants in the <em>NOTCH3</em> Gene in Russian Patients with CADASIL
• Four Novel Disease-Causing Variants in the NOTCH3 Gene in Russian Patients with CADASIL
• Gut microbes exacerbate systemic inflammation and behavior disorders in neurologic disease CADASIL
• Headache and <em>NOTCH3</em> Gene Variants in Patients with CADASIL
• Headache and NOTCH3 Gene Variants in Patients with CADASIL
• Heterogeneous blood-brain barrier dysfunction in cerebral small vessel diseases
• High Daily Diastolic Blood Pressure Predicts Incident Stroke, Lacune, and Cerebral Microbleeds in CADASIL
• Impaired cerebral interstitial fluid dynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy
• Improvement of an External Predictive Model Based on New Information Using a Synthetic Data Approach: Application to CADASIL
• Lifelong cerebrovascular disease burden among CADASIL patients: analysis from a global health research network
• Long-Term Treatment with the Calcitonin Gene-Related Peptide Receptor Antagonist Erenumab in CADASIL: Two Case Reports
• Low-frequency oscillations in the brain show differential regional associations with severity of cerebral small vessel disease: a systematic review
• Management of Inherited CNS Small Vessel Diseases: The CADASIL Example: A Scientific Statement From the American Heart Association
• Massive Microbleeds in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy
• Microbleed clustering in thalamus sign in CADASIL patients with <em>NOTCH3</em> R75P mutation
• Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation
• Middle cerebral artery dissection in a patient with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
• Most common NOTCH3 mutations causing CADASIL or CADASIL-like cerebral small vessel disease: A systematic review
• Multiple ischaemic strokes and encephalopathy in a patient with CADASIL and COVID-19: A complex association
• Multiple microbleeds in a patient with pontine autosomal dominant microangiopathy and leukoencephalopathy
• Mutant NOTCH3ECD Triggers Defects in Mitochondrial Function and Mitophagy in CADASIL Cell Models
• Nailfold capillary measurements correlated to NOTCH3 R544C mutation in preclinical CADASIL patients
• National and international collaborations to advance research into vascular contributions to cognitive decline
• Neuroimaging Characteristics of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) in Korean Based on Jeju Cohort: A Pictorial Essay
• NOTCH3 C201R variant causes cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) that can be confused with early-onset Alzheimer's disease
• NOTCH3 Variants in Patients with Suspected CADASIL
• Palliative care in CADASIL: diagnosis is only the first step
• Pathogenesis and therapeutic advances of cerebral autosomal- dominant arteriopathy with subcortical infarcts and leukoencephalopathy
• Peculiar CADASIL phenotype in monozygotic twins carrying a novel NOTCH3 pathogenetic variant
• Preimplantation Genetic Testing Inhibits the Transmission of Pathogenic Variants Associated With Cerebral White Matter Disease
• Prevalence, clinical characteristics, and risk factors of intracerebral haemorrhage in CADASIL: a case series and systematic review
• Pro-Hemorrhagic Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Associated with NOTCH3 p.R75P Mutation with Low Vascular NOTCH3 Aggregation Property
• Progress to Clarify How <em>NOTCH3</em> Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel Disease
• Progress to Clarify How NOTCH3 Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel Disease
• Protein aggregates containing wild-type and mutant NOTCH3 are major drivers of arterial pathology in CADASIL
• Recurrent depressive disorder associated with an atypical CADASIL syndrome
• Response to comments on the management and ethical implications of genetic testing in CADASIL
• Reviewing migraine-associated pathophysiology and its impact on elevated stroke risk
• SNP and Structural Study of the Notch Superfamily Provides Insights and Novel Pharmacological Targets against the CADASIL Syndrome and Neurodegenerative Diseases
• Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type 1 domain containing 1 gene mutation: a case report
• Teaching NeuroImage: CADASIL Mimicking Cerebral Amyloid Angiopathy-Related Inflammation
• The CADA-MRIT: An MRI Inventory Tool for Evaluating Cerebral Lesions in CADASIL Across Cohorts
• The cysteine-altering p.R544C variant in the NOTCH3 gene is a probable candidate for blood pressure and relevant traits in the Taiwan Biobank
• The hereditary vessel disease CADASIL
• The imaging findings of migraine with visual aura in a CADASIL patient
• The protocol for an observational Australian cohort study of CADASIL: The AusCADASIL study
• The relevance of the socio-emotional deficits in cerebral small vessels disease (CSVD): An exploratory study with sporadic CSVD and CADASIL patients
• The Roles of NOTCH3 p.R544C and Thrombophilia Genes in Vietnamese Patients With Ischemic Stroke: Study Involving a Hierarchical Cluster Analysis
• Treatment options for patients with CADASIL and large-scale cerebral infarction: mechanical thrombectomy and antiplatelet therapy-A case report
• Treatment with Cerebrolysin Prolongs Lifespan in a Mouse Model of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
• Uncovering genetic mimics in multiple sclerosis: A single-center clinical exome sequencing study
• Unveiling a Neurological Enigma: Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Presenting With Facial Palsy
• Vascular Leukoencephalopathy Associated Chorea Due to A Heterozygous Htra 1 Variant: Novel Presentation of Cadasil Type II