scholarly article | Q13442814 |
P356 | DOI | 10.1093/JNEN/NLW078 |
P698 | PubMed publication ID | 27634960 |
P2093 | author name string | Toshiro Niki | |
Shigeo Murayama | |||
Masashi Fukayama | |||
Sayaka Funabe | |||
Hiroyuki Hatsuta | |||
Shinji Ito | |||
Nobuo Ito | |||
Toshio Fukutake | |||
Imaharu Nakano | |||
Masaki Takao | |||
Yutaka Shimoe | |||
P2860 | cites work | Shifting the CARASIL paradigm: report of a non-Asian family and literature review | Q28088559 |
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Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification | Q33788625 | ||
Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome). | Q35627281 | ||
Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension | Q36709547 | ||
Neuropathological diagnostic criteria for Alzheimer's disease. | Q40475689 | ||
A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population | Q42790452 | ||
Androgen-inducible TGF-beta1 from balding dermal papilla cells inhibits epithelial cell growth: a clue to understand paradoxical effects of androgen on human hair growth | Q44192085 | ||
A novel mutation of the high-temperature requirement A serine peptidase 1 (HTRA1) gene in a Chinese family with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL). | Q44395739 | ||
Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease. | Q46040272 | ||
A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population | Q48280536 | ||
A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree | Q48406327 | ||
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | Q48665100 | ||
Clinicopathologic study of progressive subcortical vascular encephalopathy (Binswanger type) in the elderly | Q48915445 | ||
Lewy body pathology involves cutaneous nerves | Q48921589 | ||
Two novel HTRA1 mutations in a European CARASIL patient | Q56681397 | ||
P921 | main subject | Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | Q25324161 |
P577 | publication date | 2016-09-15 | |
P1433 | published in | Journal of Neuropathology & Experimental Neurology | Q15716771 |
P1476 | title | 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. |