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7. CADASIL: neuropsychological findings in three generations of an affected family. Harris JG; Filley CM J Int Neuropsychol Soc; 2001 Sep; 7(6):768-74. PubMed ID: 11575598 [TBL] [Abstract][Full Text] [Related]
10. [Japanese CADASIL case with limited dementia who had the Notch 3 R141C mutation]. Ishibashi K; Murata T; Miki Y; Hara M; Mori H No To Shinkei; 2005 May; 57(5):415-8. PubMed ID: 15981641 [TBL] [Abstract][Full Text] [Related]
11. Clinical Features of CADASIL. Abe K; Murakami T; Matsubara E; Manabe Y; Nagano I; Shoji M Ann N Y Acad Sci; 2002 Nov; 977():266-72. PubMed ID: 12480760 [TBL] [Abstract][Full Text] [Related]
13. [CADASIL: 2 case reports of hereditary multi-infarct dementia]. Otto V; Kaps M; Burgmann T; Kömpf D Fortschr Neurol Psychiatr; 1997 Feb; 65(2):90-5. PubMed ID: 9157051 [TBL] [Abstract][Full Text] [Related]
14. White matter dementia in CADASIL. Filley CM; Thompson LL; Sze CI; Simon JA; Paskavitz JF; Kleinschmidt-DeMasters BK J Neurol Sci; 1999 Mar; 163(2):163-7. PubMed ID: 10371078 [TBL] [Abstract][Full Text] [Related]
15. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification. Fukutake T J Stroke Cerebrovasc Dis; 2011; 20(2):85-93. PubMed ID: 21215656 [TBL] [Abstract][Full Text] [Related]
16. [A case of CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and lekoencephalopathy) with Notch 3 (Arg169Cys) mutation and typical granular osmiophilic materials in peripheral small arteries]. Kotani N; Hara H; Fujimura H; Miyashita T; Miyaguchi K; Tabira T Rinsho Shinkeigaku; 2004; 44(4-5):274-9. PubMed ID: 15287509 [TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant cerebral arteriopathy: neuropsychiatric syndrome in a family. Adair JC; Hart BL; Kornfeld M; Graham GD; Swanda RM; Ptacek LJ; Davis LE Neuropsychiatry Neuropsychol Behav Neurol; 1998 Jan; 11(1):31-9. PubMed ID: 9560826 [TBL] [Abstract][Full Text] [Related]
18. [Clinical characteristics of hereditary cerebrovascular disease in a large family from Colombia]. Lopera F; Arboleda J; Moreno S; Almeida N; Cuartas M; Arcos-Burgos M Rev Neurol; 2000 Nov 16-30; 31(10):901-7. PubMed ID: 11244680 [TBL] [Abstract][Full Text] [Related]
19. Very high prevalence of right-to-left shunt on transcranial Doppler in an Italian family with cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy. Angeli S; Carrera P; Del Sette M; Assini A; Grandis M; Biancolini D; Ferrari M; Gandolfo C Eur Neurol; 2001; 46(4):198-201. PubMed ID: 11721126 [TBL] [Abstract][Full Text] [Related]
20. [Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk]. Yamada H; Yasuda T; Kotorii S; Takahashi K; Tabira T; Sunada Y Rinsho Shinkeigaku; 2001; 41(2-3):144-6. PubMed ID: 11481859 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]