177 related articles for article (PubMed ID: 14730489)
1. [Clinical and neuroimaging findings in a family with CADASIL associated to C475T mutation].
Sempere AP; Pérez-Tur J; García-Barragán N; Sellés J; Medrano V; Mola S
Rev Neurol; 2004 Jan 1-15; 38(1):37-41. PubMed ID: 14730489
[TBL] [Abstract][Full Text] [Related]
2. Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Rufa A; De Stefano N; Dotti MT; Bianchi S; Sicurelli F; Stromillo ML; D'Aniello B; Federico A
Arch Neurol; 2004 Apr; 61(4):577-80. PubMed ID: 15096408
[TBL] [Abstract][Full Text] [Related]
3. CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.
Chuah TL; Tan KM; Flanagan S; Hyland V; Sullivan AA; Henderson R; MacMillan J; Lander C
J Clin Neurosci; 2001 Sep; 8(5):404-6. PubMed ID: 11535004
[TBL] [Abstract][Full Text] [Related]
4. Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation.
Tuominen S; Juvonen V; Amberla K; Jolma T; Rinne JO; Tuisku S; Kurki T; Marttila R; Pöyhönen M; Savontaus ML; Viitanen M; Kalimo H
Stroke; 2001 Aug; 32(8):1767-74. PubMed ID: 11486103
[TBL] [Abstract][Full Text] [Related]
5. [A case of early stage CADASIL showing only dizziness and vertigo with a novel mutation of Notch 3 gene].
Matsumoto H; Tsumoto M; Yamamoto T; Takahashi K; Tahira T; Ugawa Y; Tsuji S
Rinsho Shinkeigaku; 2005 Jan; 45(1):27-31. PubMed ID: 15714997
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings.
Oliveri RL; Muglia M; De Stefano N; Mazzei R; Labate A; Conforti FL; Patitucci A; Gabriele AL; Tagarelli G; Magariello A; Zappia M; Gambardella A; Federico A; Quattrone A
Arch Neurol; 2001 Sep; 58(9):1418-22. PubMed ID: 11559313
[TBL] [Abstract][Full Text] [Related]
7. Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Ruchoux MM; Domenga V; Brulin P; Maciazek J; Limol S; Tournier-Lasserve E; Joutel A
Am J Pathol; 2003 Jan; 162(1):329-42. PubMed ID: 12507916
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. A novel NOTCH3 frameshift deletion and mitochondrial abnormalities in a patient with CADASIL.
Dotti MT; De Stefano N; Bianchi S; Malandrini A; Battisti C; Cardaioli E; Federico A
Arch Neurol; 2004 Jun; 61(6):942-5. PubMed ID: 15210536
[TBL] [Abstract][Full Text] [Related]
10. An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene.
Guidetti D; Casali B; Mazzei RL; Cenacchi G; De Berti G; Zuccoli G; Nicoli D; Conforti FL; Sprovieri T; Pasquinelli G; Brini M
Neurol Sci; 2004 Feb; 24(6):401-6. PubMed ID: 14767686
[TBL] [Abstract][Full Text] [Related]
11. [CADASIL: a case with clinical, radiological, histological and genetic diagnoses].
Posada IJ; García-Morales I; Martínez MA; Hoenicka J; Bermejo F
Neurologia; 2003 May; 18(4):229-33. PubMed ID: 12721871
[TBL] [Abstract][Full Text] [Related]
12. CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia.
Kalimo H; Ruchoux MM; Viitanen M; Kalaria RN
Brain Pathol; 2002 Jul; 12(3):371-84. PubMed ID: 12146805
[TBL] [Abstract][Full Text] [Related]
13. [NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
Wang ZX; Lu H; Zhang Y; Bu DF; Niu XY; Zhang Z; Huang YN; Yuan Y
Zhonghua Yi Xue Za Zhi; 2004 Jul; 84(14):1175-80. PubMed ID: 15387979
[TBL] [Abstract][Full Text] [Related]
14. De novo mutation in the Notch3 gene causing CADASIL.
Joutel A; Dodick DD; Parisi JE; Cecillon M; Tournier-Lasserve E; Bousser MG
Ann Neurol; 2000 Mar; 47(3):388-91. PubMed ID: 10716263
[TBL] [Abstract][Full Text] [Related]
15. A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
Moon SY; Kim HY; Seok JI; Kwon JC; Ki CS; Kim JW; Suh YL; Na DL
J Korean Med Sci; 2003 Feb; 18(1):141-4. PubMed ID: 12589106
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL.
Finnilä S; Tuisku S; Herva R; Majamaa K
J Mol Med (Berl); 2001 Nov; 79(11):641-7. PubMed ID: 11715067
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. A CADASIL case with normal skin biopsy and without mutations in exons 3 and 4 of the Notch3 gene.
de Freitas GR; Miklossy J; Christen-Zäch S; Reichhart M; Bogousslavsky J
J Neurol Sci; 2001 Dec; 193(1):43-7. PubMed ID: 11718749
[TBL] [Abstract][Full Text] [Related]
20. Two Japanese CADASIL families with a R141C mutation in the Notch3 gene.
Murakami T; Iwatsuki K; Hayashi T; Sato K; Matsubara E; Nagano I; Manabe Y; Shoji M; Abe K
Intern Med; 2001 Nov; 40(11):1144-8. PubMed ID: 11757773
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]