256 related articles for article (PubMed ID: 12678157)
1. 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]
2. [A case of symptomatic cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
Nakamizo A; Koga H; Uyama E; Yamabe K
Fukuoka Igaku Zasshi; 2000 Sep; 91(9):239-42. PubMed ID: 11080925
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. [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]
6. CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Ruchoux MM; Maurage CA
J Neuropathol Exp Neurol; 1997 Sep; 56(9):947-64. PubMed ID: 9291937
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)].
Chabriat H; Joutel A; Vahedi K; Iba-Zizen MT; Tournier-Lasserve E; Bousser MG
J Mal Vasc; 1996; 21(5):277-82. PubMed ID: 9026542
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. [Hereditary autosomal dominant brain infarction].
Hagen K; Bovim G
Tidsskr Nor Laegeforen; 1998 Jun; 118(16):2483-5. PubMed ID: 9667125
[TBL] [Abstract][Full Text] [Related]
11. [Cerebral arteriopathy with subcortical infarctions and leukoencephalopathy with dominant autosomal inheritance (CADASIL). Clinical and morphological study].
Marrero Falcón C; Díez Tejedor E; Arpa Gutiérrez J; Barreiro Tella P
Neurologia; 1999; 14(6):275-82. PubMed ID: 10439621
[TBL] [Abstract][Full Text] [Related]
12. ["CADASIL"--a newly discovered hereditary cerebrovascular disease].
Søndergaard H; Jørgensen HS; Olsen TS
Ugeskr Laeger; 1998 Mar; 160(11):1617-20. PubMed ID: 9522653
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. [CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging].
Chabriat H; Joutel A; Vahedi K; Iba-Zizen MT; Tournier-Lasserve E; Bousser MG
Bull Acad Natl Med; 2000; 184(7):1523-31; discussion 1531-3. PubMed ID: 11261256
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. [Atypical CADASIL phenotypes and pathological findings in two new French families].
Mikol J; Hénin D; Baudrimont M; Gaulier A; Bacri D; Tillier JN; Davous P
Rev Neurol (Paris); 2001 Jul; 157(6-7):655-67. PubMed ID: 11458185
[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. Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL.
Hagel C; Groden C; Niemeyer R; Stavrou D; Colmant HJ
Acta Neuropathol; 2004 Sep; 108(3):231-40. PubMed ID: 15221337
[TBL] [Abstract][Full Text] [Related]
19. [Dominant autosomal cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). A review].
Navarro E; Díaz F; Muñoz L; Giménez-Roldán S
Neurologia; 2002 Oct; 17(8):410-7. PubMed ID: 12396971
[TBL] [Abstract][Full Text] [Related]
20. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a Greek family.
Mandellos D; Limbitaki G; Papadimitriou A; Anastasopoulos D
Neurol Sci; 2005 Oct; 26(4):278-81. PubMed ID: 16193256
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]