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A Case of CADASIL with NOTCH3 Gene Mutation Presenting with Focal Epileptic Seizure: A Case of CADASIL Presenting with Focal Epileptic Seizure.
- Published in:
- Archives of Epilepsy, 2023, v. 29, n. 1, p. 34, doi. 10.4274/ArchEpilepsy.2023.22025
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- Publication type:
- Article
Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-86349-1
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- Publication type:
- Article
Chinese guideline for the diagnosis and management of CADASIL (2022 edition): a protocol.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2023, v. 23, n. 11, p. 959, doi. 10.3969/j.issn.1672-6731.2023.11.002
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- Publication type:
- Article
Pathological changes and molecular-genetic mechanisms of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2021, v. 21, n. 10, p. 828, doi. 10.3969/j.issn.1672-6731.2021.10.002
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- Publication type:
- Article
Clinical features of cognitive function in eight patients with hereditary cerebral small vessel disease.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2019, v. 19, n. 8, p. 559, doi. 10.3969/j.issn.1672-6731.2019.08.005
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- Publication type:
- Article
CADASIL as a Multiple Sclerosis Mimic.
- Published in:
- 2017
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- Publication type:
- Case Study
Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
- Published in:
- Turkish Journal of Neurology / Turk Noroloji Dergisi, 2021, v. 17, n. 3, p. 240, doi. 10.4274/tnd.2021.91298
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- Publication type:
- Article
Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASIL.
- Published in:
- International Journal of Molecular Sciences, 2017, v. 18, n. 9, p. 1964, doi. 10.3390/ijms18091964
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- Publication type:
- Article
Case report: bipolar disorder as the first manifestation of CADASIL.
- Published in:
- BMC Psychiatry, 2014, v. 14, n. 1, p. 139, doi. 10.1186/1471-244X-14-175
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- Publication type:
- Article
Neuromyelitis optica spectrum disorder mimicking cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy with symmetrical lesions in the temporal poles and external capsules on MRI.
- Published in:
- Neuroradiology, 2024, v. 66, n. 11, p. 1887, doi. 10.1007/s00234-024-03458-0
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- Publication type:
- Article
Detection of early neuronal damage in CADASIL patients by q-space MR imaging.
- Published in:
- Neuroradiology, 2013, v. 55, n. 3, p. 283, doi. 10.1007/s00234-012-1105-x
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- Publication type:
- Article
An Unsuspecting Recurrent Cryptogenic Stroke: A Case Report.
- Published in:
- 2021
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- Publication type:
- Case Study
A Review of Neuroimaging in Rare Neurodegenerative Diseases.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2020, v. 49, n. 6, p. 544, doi. 10.1159/000512543
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- Publication type:
- Article
The NOTCH3 score: a pre-clinical CADASIL biomarker in a novel human genomic NOTCH3 transgenic mouse model with early progressive vascular NOTCH3 accumulation.
- Published in:
- Acta Neuropathologica Communications, 2015, v. 3, p. 1, doi. 10.1186/s40478-015-0268-1
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- Publication type:
- Article
CADASIL: Ultrastructural insights into the morphology of granular osmiophilic material.
- Published in:
- Brain & Behavior, 2017, v. 7, n. 3, p. n/a, doi. 10.1002/brb3.624
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- Publication type:
- Article
Novel mutation of the notch3 gene in arabic family with CADASIL.
- Published in:
- Neurology International, 2011, v. 3, n. 2, p. 22, doi. 10.4081/ni.2011.e6
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- Publication type:
- Article
Poster 449: Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Mimicking Multiple Sclerosis: A Case Report.
- Published in:
- 2010
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- Publication type:
- Abstract
Poster 381: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) ‐ A Rare Diagnosis in Siblings: A Case Series.
- Published in:
- 2009
- By:
- Publication type:
- Abstract
Clinical and Radiological Features in CADASIL and NOTCH3-Negative Patients: A Multicenter Study from Turkey.
- Published in:
- European Neurology, 2014, v. 72, n. 3/4, p. 125, doi. 10.1159/000360530
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- Publication type:
- Article
Genetic study of the NOTCH3 gene in CADASIL patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2018, v. 19, n. 4, p. 425, doi. 10.1016/j.ejmhg.2018.05.001
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- Publication type:
- Article
Dopamine differently modulates central cholinergic circuits in patients with Alzheimer disease and CADASIL.
- Published in:
- Journal of Neural Transmission, 2014, v. 121, n. 10, p. 1313, doi. 10.1007/s00702-014-1195-1
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- Publication type:
- Article
CADASIL Type 2 (HTRA1 Cerebral Small Vessel Disease) in an Indian Woman.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Fusiform intracranial aneurysms in a CADASIL patient: A possibly missed association.
- Published in:
- 2022
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- Publication type:
- Case Study
CADASIL and cavernomas: A common mechanism.
- Published in:
- 2020
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- Publication type:
- Case Study
CARASIL; The backache, baldness, brain attack syndrome: The Indian scenario.
- Published in:
- 2020
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- Publication type:
- Case Study
An unusual case of cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy with occipital lobe involvement.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Cadasil coma: Unusual cause for acute encephalopathy.
- Published in:
- 2015
- By:
- Publication type:
- Letter to the Editor
Reducing Timp3 or vitronectin ameliorates disease manifestations in CADASIL mice.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Pericytes are involved in the pathogenesis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
- Published in:
- 2015
- By:
- Publication type:
- journal article
MRI Findings in a Case of Genetically Proven CADASIL with Emphasis on Differential Diagnosis.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
Sporadic CADASIL: A Rare Occurrence.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
Characteristics of CADASIL in Chinese mainland patients.
- Published in:
- Neurology India, 2014, v. 62, n. 3, p. 257, doi. 10.4103/0028-3886.136900
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- Publication type:
- Article
CADASIL mutant NOTCH3(R90C) decreases the viability of HS683 oligodendrocytes via apoptosis.
- Published in:
- Molecular Biology Reports, 2017, v. 44, n. 3, p. 273, doi. 10.1007/s11033-017-4107-2
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- Publication type:
- Article
Multifocal Cerebral and Bilateral Middle Cerebellar Peduncle Infarctions in CADASIL.
- Published in:
- Canadian Journal of Neurological Sciences, 2016, v. 43, n. 4, p. 574, doi. 10.1017/cjn.2016.5
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- Publication type:
- Article
CADASIL with Multiorgan Involvement: a Complete Autopsy Examination Report.
- Published in:
- Canadian Journal of Neurological Sciences, 2016, v. 43, n. 1, p. 202, doi. 10.1017/cjn.2015.240
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- Publication type:
- Article
A CADASIL-Like Case with a Novel Noncysteine Mutation of the NOTCH3 Gene and Granular Deposits in the Renal Arterioles.
- Published in:
- Case Reports in Neurological Medicine, 2015, v. 2015, p. 1, doi. 10.1155/2015/431461
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- Publication type:
- Article
Clinical variability of the cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in two siblings of a large family showing the same mutation.
- Published in:
- International Medical Case Reports Journal, 2013, v. 5, p. 59, doi. 10.2147/IMCRJ.S51875
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- Publication type:
- Article
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL).
- Published in:
- Journal of Clinical & Aesthetic Dermatology, 2013, v. 6, n. 3, p. 29
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- Publication type:
- Article
March Highlights.
- Published in:
- Journal of Clinical & Aesthetic Dermatology, 2013, v. 6, n. 3, p. 12
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- Publication type:
- Article
Impaired cerebral interstitial fluid dynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.
- Published in:
- Brain Communications, 2024, v. 6, n. 1, p. 1, doi. 10.1093/braincomms/fcad349
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- Publication type:
- Article
A Report of Accelerated Coronary Artery Disease Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
- Published in:
- Case Reports in Cardiology, 2015, v. 2015, p. 1, doi. 10.1155/2015/167513
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- Publication type:
- Article
Cerebral Microbleeds, Hypertension, and Intracerebral Hemorrhage in Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
- Published in:
- Frontiers in Neurology, 2017, p. 1, doi. 10.3389/fneur.2017.00203
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- Publication type:
- Article
CADASIL presenting with spontaneous intracerebral hemorrhage: report of a case and description of the first family in Northern Greece.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles.
- Published in:
- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0136501
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- Publication type:
- Article
R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL.
- Published in:
- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0135470
- By:
- Publication type:
- Article
Multimodal Retinal Vessel Analysis in CADASIL Patients.
- Published in:
- PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0112311
- By:
- Publication type:
- Article
In Vivo High-Resolution 7 Tesla MRI Shows Early and Diffuse Cortical Alterations in CADASIL.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0106311
- By:
- Publication type:
- Article
A Novel Cysteine-Sparing <i>NOTCH3</i> Mutation in a Chinese Family with CADASIL.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104533
- By:
- Publication type:
- Article
Is the Oxidant/Antioxidant Status Altered in CADASIL Patients?
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0067077
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- Publication type:
- Article
Role of Electron Microscopy in the Diagnosis of Cadasil Syndrome: A Study of 32 Patients.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065482
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- Publication type:
- Article