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.

scientific article published on 15 September 2016

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. is …
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scholarly articleQ13442814

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P356DOI10.1093/JNEN/NLW078
P698PubMed publication ID27634960

P2093author name stringToshiro Niki
Shigeo Murayama
Masashi Fukayama
Sayaka Funabe
Hiroyuki Hatsuta
Shinji Ito
Nobuo Ito
Toshio Fukutake
Imaharu Nakano
Masaki Takao
Yutaka Shimoe
P2860cites workShifting the CARASIL paradigm: report of a non-Asian family and literature reviewQ28088559
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Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identificationQ33788625
Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome).Q35627281
Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertensionQ36709547
Neuropathological diagnostic criteria for Alzheimer's disease.Q40475689
A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian populationQ42790452
Androgen-inducible TGF-beta1 from balding dermal papilla cells inhibits epithelial cell growth: a clue to understand paradoxical effects of androgen on human hair growthQ44192085
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 populationQ48280536
A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigreeQ48406327
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathyQ48665100
Clinicopathologic study of progressive subcortical vascular encephalopathy (Binswanger type) in the elderlyQ48915445
Lewy body pathology involves cutaneous nervesQ48921589
Two novel HTRA1 mutations in a European CARASIL patientQ56681397
P921main subjectCerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathyQ25324161
P577publication date2016-09-15
P1433published inJournal of Neuropathology & Experimental NeurologyQ15716771
P1476titleHistopathologic 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.