Found: 123
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Nuclear abnormalities in vascular myocytes in cerebral autosomal‐dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
- Published in:
- Neuropathology, 2018, v. 38, n. 6, p. 601, doi. 10.1111/neup.12519
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- Publication type:
- Article
Pericytes as a new target for pathological processes in CADASIL.
- Published in:
- Neuropathology, 2012, v. 32, n. 5, p. 515, doi. 10.1111/j.1440-1789.2011.01290.x
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- Publication type:
- Article
Glial vascular degeneration in CADASIL.
- Published in:
- 2010
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- Publication type:
- journal 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
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
Location, number and factors associated with cerebral microbleeds in an Italian-British cohort of CADASIL patients.
- Published in:
- PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0190878
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- Publication type:
- Article
Do Attachment Style and Emotion Regulation Strategies Indicate Distress in Predictive Testing?
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- Journal of Genetic Counseling, 2015, v. 24, n. 5, p. 862, doi. 10.1007/s10897-015-9822-z
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- Publication type:
- Article
Alzheimer's disease and CADASIL are heritable, adult-onset dementias that both involve damaged small blood vessels.
- Published in:
- Cellular & Molecular Life Sciences, 2014, v. 71, n. 6, p. 949, doi. 10.1007/s00018-013-1542-7
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- Publication type:
- Article
Fatal familial insomnia with abnormal signals on routine MRI: a case report and literature review.
- Published in:
- 2017
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- Publication type:
- journal article
MRI Findings in a Case of Genetically Proven CADASIL with Emphasis on Differential Diagnosis.
- Published in:
- 2019
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- Publication type:
- case study
Sporadic CADASIL: A Rare Occurrence.
- Published in:
- 2019
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- 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
Diffusion Tensor Imaging to Map Brain Microstructural Changes in CADASIL.
- Published in:
- 2017
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- Publication type:
- journal 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
Acute Simultaneous Multiple Diffusion‐Weighted MRI Abnormalities in a Patient With CADASIL.
- Published in:
- 2018
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- Publication type:
- Case Study
Abstracts and Citations.
- Published in:
- Headache: The Journal of Head & Face Pain, 2016, v. 56, n. 5, p. 897, doi. 10.1111/head.12786
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- Publication type:
- Article
Migraine, Chronic Vasculopathies, and Spreading Depolarization.
- Published in:
- Headache: The Journal of Head & Face Pain, 2016, v. 56, n. 3, p. 580, doi. 10.1111/head.12753
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- Publication type:
- Article
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations.
- Published in:
- 2016
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- Publication type:
- journal article
Depressive symptoms as a predictor of quality of life in cerebral small vessel disease, acting independently of disability; a study in both sporadic small vessel disease and CADASIL.
- Published in:
- International Journal of Stroke, 2013, v. 8, n. 7, p. 510, doi. 10.1111/j.1747-4949.2011.00763.x
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- Publication type:
- Article
Reducing Timp3 or vitronectin ameliorates disease manifestations in CADASIL mice.
- Published in:
- 2016
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- Publication type:
- journal article
Pericytes are involved in the pathogenesis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
- Published in:
- 2015
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- Publication type:
- journal 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
The comparisons of phenotype and genotype between CADASIL and CADASIL-like patients and population-specific evaluation of CADASIL scale in China.
- Published in:
- Journal of Headache & Pain, 2016, v. 17, n. 1, p. 1, doi. 10.1186/s10194-016-0646-5
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- Publication type:
- Article
CADASIL brain vessels show a HTRA1 loss-of-function profile.
- Published in:
- Acta Neuropathologica, 2018, v. 136, n. 1, p. 111, doi. 10.1007/s00401-018-1853-8
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- Publication type:
- Article
Genotype phenotype correlation of cadasil patients-single center experience.
- Published in:
- Annals of Medical of Research, 2021, v. 28, n. 2, p. 381, doi. 10.5455/annalsmedres.2020.08.886
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- Publication type:
- Article
An Unsuspecting Recurrent Cryptogenic Stroke: A Case Report.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Altered dynamics of neurovascular coupling in CADASIL.
- Published in:
- Annals of Clinical & Translational Neurology, 2018, v. 5, n. 7, p. 788, doi. 10.1002/acn3.574
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- Publication type:
- Article
CADASIL: two new cases with intracerebral hemorrhage.
- Published in:
- Annals of Clinical & Translational Neurology, 2017, v. 4, n. 4, p. 266, doi. 10.1002/acn3.400
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- Publication type:
- Article
Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL.
- Published in:
- Annals of Clinical & Translational Neurology, 2016, v. 3, n. 11, p. 844, doi. 10.1002/acn3.344
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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
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
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
Clinical spectrum in CADASIL family with a new mutation.
- Published in:
- Biomedical Papers of the Medical Faculty of Palacky University in Olomouc, 2013, v. 157, n. 4, p. 379, doi. 10.5507/bp.2013.055
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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
Peripheral neuropathy in a case with CADASIL: a case report.
- Published in:
- 2018
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- Publication type:
- journal article
Increased PKR level in human CADASIL brains.
- Published in:
- 2018
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- Publication type:
- journal 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
Cerebral Autosomal‐Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Syndrome, a Central Nervous System Vasculitis Mimic.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
İki Uçlu Bozukluk Şeklinde Ortaya Çıkan CADASIL Sendromu.
- Published in:
- 2012
- By:
- Publication type:
- Case Study
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
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
The role of clinical and neuroimaging features in the diagnosis of CADASIL.
- Published in:
- Journal of Neurology, 2018, v. 265, n. 12, p. 2934, doi. 10.1007/s00415-018-9072-8
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- Publication type:
- Article
A novel frameshift variant in the CADASIL gene NOTCH3: pathogenic or not?
- Published in:
- Journal of Neurology, 2018, v. 265, n. 6, p. 1338, doi. 10.1007/s00415-018-8844-5
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- Publication type:
- Article
Monogenic causes of stroke: now and the future.
- Published in:
- Journal of Neurology, 2015, v. 262, n. 12, p. 2601, doi. 10.1007/s00415-015-7794-4
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- Publication type:
- Article
A novel HTRA1 exon 2 mutation causes loss of protease activity in a Pakistani CARASIL patient.
- Published in:
- 2015
- By:
- Publication type:
- Letter
CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients.
- Published in:
- Journal of Neurology, 2015, v. 262, n. 1, p. 134, doi. 10.1007/s00415-014-7533-2
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- Publication type:
- Article
Presymptomatic genetic testing in CADASIL.
- Published in:
- Journal of Neurology, 2012, v. 259, n. 10, p. 2131, doi. 10.1007/s00415-012-6468-8
- By:
- Publication type:
- Article
Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL.
- Published in:
- Journal of Headache & Pain, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s10194-019-1052-6
- By:
- Publication type:
- Article