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4. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: MR findings. Skehan SJ; Hutchinson M; MacErlaine DP AJNR Am J Neuroradiol; 1995; 16(10):2115-9. PubMed ID: 8585503 [TBL] [Abstract][Full Text] [Related]
5. A family with autosomal dominant, non-Alzheimer's presenile dementia. Dark F Aust N Z J Psychiatry; 1997 Feb; 31(1):139-44. PubMed ID: 9088499 [TBL] [Abstract][Full Text] [Related]
6. [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]
7. [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]
8. Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease. Sourander P; Wålinder J Acta Neuropathol; 1977 Aug; 39(3):247-54. PubMed ID: 906807 [TBL] [Abstract][Full Text] [Related]
9. Sneddon syndrome presenting with hemicranic attacks: a case report. Martinelli A; Martinelli P; Ippoliti M; Giuliani S; Coccagna G Acta Neurol Scand; 1991 Mar; 83(3):201-3. PubMed ID: 1815538 [TBL] [Abstract][Full Text] [Related]
10. [Analysis of complex segregation in a large family with hereditary cerebrovascular disease in Antioquia, Colombia]. Lopera F; Rivera N; Arboleda J; Restrepo T; Arcos-Burgos M Rev Neurol; 2001 Feb 1-15; 32(3):222-5. PubMed ID: 11310272 [TBL] [Abstract][Full Text] [Related]
13. Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneity. St Clair D; Bolt J; Morris S; Doyle D J Med Genet; 1995 Jan; 32(1):57-60. PubMed ID: 7897629 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. [From gene to disease; from Notch3 to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]. Oberstein SA; Bakker E; Ferrari MD; Haan J Ned Tijdschr Geneeskd; 2001 Feb; 145(8):359-60. PubMed ID: 11257815 [TBL] [Abstract][Full Text] [Related]
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17. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Tournier-Lasserve E; Joutel A; Melki J; Weissenbach J; Lathrop GM; Chabriat H; Mas JL; Cabanis EA; Baudrimont M; Maciazek J Nat Genet; 1993 Mar; 3(3):256-9. PubMed ID: 8485581 [TBL] [Abstract][Full Text] [Related]
18. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a positron emission tomography study in two affected family members. Chabriat H; Bousser MG; Pappata S Stroke; 1995 Sep; 26(9):1729-30. PubMed ID: 7660422 [No Abstract] [Full Text] [Related]
19. Mutation of the Notch 3 gene in a Thai cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy family. Suwanwela N; Srikiatkhachorn A; Tangwongchai S; Phanthumchina K; Suwanwela N J Med Assoc Thai; 2003 Feb; 86(2):178-82. PubMed ID: 12678157 [TBL] [Abstract][Full Text] [Related]