| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1046/J.1440-1789.2003.00519.X |
| P698 | PubMed publication ID | 14719550 |
| P2093 | author name string | Kunimasa Arima | |
| Nobuo Ito | |||
| Shu-ichi Ikeda | |||
| Sohei Yanagawa | |||
| P2860 | cites work | Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia | Q28294011 |
| Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis | Q34106491 | ||
| Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy | Q34295928 | ||
| Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: phenotypic and mutational spectrum | Q34989471 | ||
| Mutations of the notch3 gene in non-caucasian patients with suspected CADASIL syndrome | Q43539551 | ||
| Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis | Q44480153 | ||
| Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study | Q48365396 | ||
| Arterial changes in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in relation to pathogenesis of diffuse myelin loss of cerebral white matter: examination of cerebral medullary arteries by recon | Q48456062 | ||
| Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | Q48665100 | ||
| Diagnostic strategies in CADASIL | Q78415468 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 327-334 | |
| P577 | publication date | 2003-12-01 | |
| P1433 | published in | Neuropathology | Q15761930 |
| P1476 | title | Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome). | |
| P478 | volume | 23 |
| Q39383329 | A CARASIL Patient from Americas with Novel Mutation and Atypical Features: Case Presentation and Literature Review |
| Q48406327 | A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree |
| Q85000670 | Absence of small-vessel abnormalities in alternating hemiplegia of childhood |
| Q30861866 | CADASIL and CARASIL. |
| Q37789495 | Cognitive impairment of vascular origin: Neuropathology of cognitive impairment of vascular origin |
| Q93102418 | Genetic Factors of Cerebral Small Vessel Disease and Their Potential Clinical Outcome |
| Q35094704 | Genetics of Vascular Dementia |
| Q39429524 | Genetics of ischaemic stroke |
| Q26775633 | Genetics of ischaemic stroke in young adults |
| Q51499978 | Histopathologic Analysis of Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL): A Report of a New Genetically Confirmed Case and Comparison to 2 Previous Cases. |
| Q55451622 | Loss of HtrA1 serine protease induces synthetic modulation of aortic vascular smooth muscle cells. |
| Q43228018 | Loss of HtrA1-induced attenuation of TGF-β signaling in fibroblasts might not be the main mechanism of CARASIL pathogenesis. |
| Q38513520 | Monogenic causes of stroke: now and the future |
| Q36853643 | Monogenic vessel diseases related to ischemic stroke: a clinical approach |
| Q37808273 | Review: molecular genetics and pathology of hereditary small vessel diseases of the brain. |
| Q38004977 | Single gene disorders associated with stroke: a review and update on treatment options |
| Q36522909 | Single gene disorders causing ischaemic stroke |
| Q49076465 | The neuropathology of vascular and mixed dementia and vascular cognitive impairment |
| Q36933027 | The role of genetics in stroke |
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