123 related articles for article (PubMed ID: 12574530)
1. Stroke genetics update.
Alberts MJ
Stroke; 2003 Feb; 34(2):342-4. PubMed ID: 12574530
[No Abstract] [Full Text] [Related]
2. Advances in molecular genetics and pathology of cerebrovascular disorders.
Kalaria RN
Trends Neurosci; 2001 Jul; 24(7):392-400. PubMed ID: 11410270
[TBL] [Abstract][Full Text] [Related]
3. A 52-year-old man with cognitive decline, seizure and stroke.
Simon JE; Parboosingh J; Clark A; George D; Lafontaine AL; Hill MD
CMAJ; 2004 Apr; 170(9):1393-4. PubMed ID: 15111470
[No Abstract] [Full Text] [Related]
4. [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]
5. An animal model for the molecular genetics of CADASIL. (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy).
Fryxell KJ; Soderlund M; Jordan TV
Stroke; 2001 Jan; 32(1):6-11. PubMed ID: 11136906
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Description of a simple test for CADASIL disease and determination of mutation frequencies in sporadic ischaemic stroke and dementia patients.
Wang T; Sharma SD; Fox N; Rossor M; Brown MJ; Sharma P
J Neurol Neurosurg Psychiatry; 2000 Nov; 69(5):652-4. PubMed ID: 11032621
[TBL] [Abstract][Full Text] [Related]
8. Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families.
Thomas NJ; Morris CM; Scaravilli F; Johansson J; Rossor M; De Lange R; St Clair D; Nicoll J; Blank C; Coulthard A; Bushby K; Ince PG; Burn D; Kalaria RN
Ann N Y Acad Sci; 2000 Apr; 903():293-8. PubMed ID: 10818518
[TBL] [Abstract][Full Text] [Related]
9. Association study of Notch 4 polymorphisms with Alzheimer's disease.
Lambert JC; Mann D; Harris J; Araria-Goumidi L; Chartier-Harlin MC; Cottel D; Iwatsubo T; Amouyel P; Lendon C
J Neurol Neurosurg Psychiatry; 2004 Mar; 75(3):377-81. PubMed ID: 14966150
[TBL] [Abstract][Full Text] [Related]
10. Gene symbol: NOTCH3. Disease: CADASIL.
Rojas-Marcos I; Encarnacion M; Martinez-Yelamos S; Ferrer I; Arbizu T; Gil-Peralta A; Garcia-Lozano JR
Hum Genet; 2004 Jul; 115(2):175. PubMed ID: 15300988
[No Abstract] [Full Text] [Related]
11. Mouse Notch 3 expression in the pre- and postnatal brain: relationship to the stroke and dementia syndrome CADASIL.
Prakash N; Hansson E; Betsholtz C; Mitsiadis T; Lendahl U
Exp Cell Res; 2002 Aug; 278(1):31-44. PubMed ID: 12126955
[TBL] [Abstract][Full Text] [Related]
12. Screening British CADASIL families for mutations in the NOTCH3 gene.
de Lange RP; Bolt J; Reid E; da Silva R; Shaw DJ; St Clair DM
J Med Genet; 2000 Mar; 37(3):224-5. PubMed ID: 10777367
[No Abstract] [Full Text] [Related]
13. CADASIL: a monogenic condition causing stroke and subcortical vascular dementia.
Dichgans M
Cerebrovasc Dis; 2002; 13 Suppl 2():37-41. PubMed ID: 11901241
[TBL] [Abstract][Full Text] [Related]
14. Genetic analysis of the (CTG)n NOTCH4 polymorphism in 65 multiplex bipolar pedigrees.
Swift-Scanlan T; Lan TH; Fallin MD; Coughlin JM; Potash JB; DePaulo JR; McInnis MG
Psychiatr Genet; 2002 Mar; 12(1):43-7. PubMed ID: 11901359
[TBL] [Abstract][Full Text] [Related]
15. Age-dependent association of apolipoprotein E genotypes with stroke subtypes in a Japanese rural population.
Kokubo Y; Chowdhury AH; Date C; Yokoyama T; Sobue H; Tanaka H
Stroke; 2000 Jun; 31(6):1299-306. PubMed ID: 10835448
[TBL] [Abstract][Full Text] [Related]
16. Notch4 gene polymorphisms are not associated with autism in Japanese population.
Koishi S; Yamazaki K; Yamamoto K; Koishi S; Enseki Y; Nakamura Y; Oya A; Yasueda M; Asakura A; Aoki Y; Atsumi M; Inomata J; Inoko H; Matsumoto H
Am J Med Genet B Neuropsychiatr Genet; 2004 Feb; 125B(1):61-2. PubMed ID: 14755446
[No Abstract] [Full Text] [Related]
17. Diagnostic strategies in CADASIL.
Razvi SS; Davidson R; Bone I; Muir KW
Neurology; 2003 Jun; 60(12):2019-20; author reply 2020. PubMed ID: 12821764
[No Abstract] [Full Text] [Related]
18. Diagnostic strategies in CADASIL.
Oberstein SA
Neurology; 2003 Jun; 60(12):2020; author reply 2020. PubMed ID: 14710716
[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]
20. CADASIL Notch3 mutant proteins localize to the cell surface and bind ligand.
Haritunians T; Boulter J; Hicks C; Buhrman J; DiSibio G; Shawber C; Weinmaster G; Nofziger D; Schanen C
Circ Res; 2002 Mar; 90(5):506-8. PubMed ID: 11909813
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]