Disease: CADASIL
- <em>NOTCH2NLC</em> GGC Repeat Expansion in Patients With Vascular Leukoencephalopathy
- <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 novel report of Cys1298Gly mutation in exon 24 of NOTCH3 gene in a Chinese family with CADASIL
- Acute bilateral multiple subcortical infarcts as manifestation in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- Acute Fatal Leukoencephalopathic Presentation of CADASIL
- 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
- Antiplatelet use and CADASIL: a retrospective observational analysis
- 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: A NOTCH3-associated cerebral small vessel disease
- Case report: Mild leukoencephalopathy caused by a new mutation of NOTCH3 gene
- Cerebral Autosomal Dominant Arteriopathy
- 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 During the Postpartum Period as Postpartum Depression and Postpartum Psychosis
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Atypical clinical presentation with isolated frontotemporal dementia
- Chorea Associated with Genetic-Confirmed CADASIL
- Clinical and epidemiological profiles from a case series of 26 Brazilian CADASIL patients
- 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 of a CADASIL point mutation using adenine base editors in hiPSCs and blood vessel organoids
- Correction to: Modeling CADASIL vascular pathologies with patient-derived induced pluripotent stem cells
- 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
- 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
- Diagnostic challenges in CADASIL
- Diffusion prepared pseudo-continuous arterial spin labeling reveals blood-brain barrier dysfunction in patients with CADASIL
- Disturbances of Ocular Circulation in Color Doppler Imaging, Retinal Changes and Electrophysiological Tests with Neuro-Ophthalmological Clinical Symptoms in the Course of CADASIL Syndrome-A Case Report
- 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
- ER stress induced immunopathology involving complement in CADASIL: implications for therapeutics
- Exonic mutations in cell-cell adhesion may contribute to CADASIL-related CSVD pathology
- 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
- 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
- Induced pluripotent stem cell model revealed impaired neurovascular interaction in genetic small vessel disease Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Inflammatory Optic Neuropathy as a Presenting Feature of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy
- 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 Coronary Artery Disease in CADASIL Patients: Review of Current Literature
- 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
- Modifiable Vascular Risk Factors Contribute to Stroke in 1,080 NOTCH3 R544C Carriers in Taiwan Biobank
- Modifiable vascular risk factors contribute to stroke in 1080 <em>NOTCH3</em> R544C carriers in Taiwan Biobank
- Multiple ischaemic strokes and encephalopathy in a patient with CADASIL and COVID-19: A complex association
- 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
- Novel grading system for CADASIL severity: A multicenter cross-sectional study
- Palliative care in CADASIL: diagnosis is only the first step
- Parkinsonism Following SARS-CoV-2 Infection Unmasks a Genetic Twist
- 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
- Presumed periventricular venous infarction on magnetic resonance imaging and its association with increased white matter edema in CADASIL
- Prevalence, clinical characteristics, and risk factors of intracerebral haemorrhage in CADASIL: a case series and systematic review
- 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
- Retinal vascular density in CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy)
- Segmentation of incident lacunes during the course of ischemic cerebral small vessel diseases
- Spontaneous coronary artery dissection with leucoencephalopathy associated with thrombospondin Type 1 domain containing 1 gene mutation: a case report
- Structural changes in NOTCH3 induced by CADASIL mutations: Role of cysteine and non-cysteine alterations
- 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 EffecTs of Amlodipine and other Blood PREssure Lowering Agents on Microvascular FuncTion in Small Vessel Diseases (TREAT-SVDs) trial: Study protocol for a randomised crossover trial
- The imaging findings of migraine with visual aura in a CADASIL patient
- The relevance of the socio-emotional deficits in cerebral small vessels disease (CSVD): An exploratory study with sporadic CSVD and CADASIL patients
- The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay
- Treatment with Cerebrolysin Prolongs Lifespan in a Mouse Model of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy