These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
447 related articles for article (PubMed ID: 18499132)
1. Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene. Pradotto L; Azan G; Doriguzzi C; Valentini C; Mauro A J Neurol Sci; 2008 Aug; 271(1-2):207-10. PubMed ID: 18499132 [TBL] [Abstract][Full Text] [Related]
2. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a patient from Sri Lanka. De Silva KR; Gamage R; Dunuwille J; Gunarathna D; Sirisena D; Weerasinghe A; Amarasinghe PH; Hosomi A; Mizuno T J Clin Neurosci; 2009 Nov; 16(11):1492-3. PubMed ID: 19683925 [TBL] [Abstract][Full Text] [Related]
3. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) associated with a novel C82R mutation in the NOTCH3 gene. Zea-Sevilla MA; Bermejo-Velasco P; Serrano-Heranz R; Calero M J Alzheimers Dis; 2015; 43(2):363-7. PubMed ID: 25096610 [TBL] [Abstract][Full Text] [Related]
4. A new de novo Notch3 mutation causing CADASIL. Coto E; Menéndez M; Navarro R; García-Castro M; Alvarez V Eur J Neurol; 2006 Jun; 13(6):628-31. PubMed ID: 16796587 [TBL] [Abstract][Full Text] [Related]
5. A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient. Pescini F; Bianchi S; Salvadori E; Poggesi A; Dotti MT; Federico A; Inzitari D; Pantoni L J Neurol Sci; 2008 Apr; 267(1-2):170-3. PubMed ID: 18022198 [TBL] [Abstract][Full Text] [Related]
6. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese. Lee YC; Yang AH; Liu HC; Wong WJ; Lu YC; Chang MH; Soong BW J Neurol Sci; 2006 Jul; 246(1-2):111-5. PubMed ID: 16580020 [TBL] [Abstract][Full Text] [Related]
7. Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients. Pantoni L; Pescini F; Nannucci S; Sarti C; Bianchi S; Dotti MT; Federico A; Inzitari D Neurology; 2010 Jan; 74(1):57-63. PubMed ID: 20038773 [TBL] [Abstract][Full Text] [Related]
8. Therapeutic NOTCH3 cysteine correction in CADASIL using exon skipping: in vitro proof of concept. Rutten JW; Dauwerse HG; Peters DJ; Goldfarb A; Venselaar H; Haffner C; van Ommen GJ; Aartsma-Rus AM; Lesnik Oberstein SA Brain; 2016 Apr; 139(Pt 4):1123-35. PubMed ID: 26912635 [TBL] [Abstract][Full Text] [Related]
9. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)]. Ueda M; Nakaguma R; Ando Y Rinsho Byori; 2009 Mar; 57(3):242-51. PubMed ID: 19363995 [TBL] [Abstract][Full Text] [Related]
10. A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family. Pavlovic AM; Dobricic V; Semnic R; Lackovic V; Novakovic I; Bajcetic M; Sternic N Acta Neurol Belg; 2013 Sep; 113(3):299-302. PubMed ID: 23319290 [TBL] [Abstract][Full Text] [Related]
11. New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Abramycheva N; Stepanova M; Kalashnikova L; Zakharova M; Maximova M; Tanashyan M; Lagoda O; Fedotova E; Klyushnikov S; Konovalov R; Sakharova A; Illarioshkin S J Neurol Sci; 2015 Feb; 349(1-2):196-201. PubMed ID: 25623805 [TBL] [Abstract][Full Text] [Related]
12. Two novel mutations of the NOTCH3 gene in Korean patients with CADASIL. Kim Y; Kim JS; Kim G; No YJ; Yoo HW Mutat Res; 2006 Jan; 593(1-2):116-20. PubMed ID: 16256149 [TBL] [Abstract][Full Text] [Related]
13. CADASIL and autoimmunity: coexistence in a family with the R169C mutation at exon 4 of the NOTCH3 gene. Paraskevas GP; Bougea A; Synetou M; Vassilopoulou S; Anagnostou E; Voumvourakis K; Iliopoulos A; Spengos K Cerebrovasc Dis; 2014; 38(4):302-7. PubMed ID: 25412914 [TBL] [Abstract][Full Text] [Related]
14. [A new Spanish family with CADASIL associated with 346C>T mutation of NOTCH3 gene]. Avila A; Bello J; Maho P; Gómez MI Neurologia; 2007 Sep; 22(7):484-7. PubMed ID: 17853970 [TBL] [Abstract][Full Text] [Related]
15. A novel CADASIL-causing mutation in a stroke patient. Vikelis M; Papatriantafyllou J; Karageorgiou CE Swiss Med Wkly; 2007 Jun; 137(21-22):323-5. PubMed ID: 17629811 [TBL] [Abstract][Full Text] [Related]
16. Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit? Guerrot D; François A; Boffa JJ; Boulos N; Hanoy M; Legallicier B; Triquenot-Bagan A; Guyant-Marechal L; Laquerriere A; Freguin-Bouilland C; Ronco P; Godin M Am J Kidney Dis; 2008 Aug; 52(2):340-5. PubMed ID: 18572291 [TBL] [Abstract][Full Text] [Related]
17. The R110C mutation in Notch3 causes variable clinical features in two Turkish families with CADASIL syndrome. Uyguner ZO; Siva A; Kayserili H; Saip S; Altintaş A; Apak MY; Albayram S; Işik N; Akman-Demir G; Taşyürekli M; Oz B; Wollnik B J Neurol Sci; 2006 Jul; 246(1-2):123-30. PubMed ID: 16730748 [TBL] [Abstract][Full Text] [Related]
18. CADASIL with NOTCH3 S180C presenting anticipation of onset age and hallucinations. Nakamura T; Watanabe H; Hirayama M; Inukai A; Kabasawa H; Matsubara M; Mitake S; Nakamura M; Ando Y; Uchino M; Sobue G J Neurol Sci; 2005 Nov; 238(1-2):87-91. PubMed ID: 16111703 [TBL] [Abstract][Full Text] [Related]
19. Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation. Ragno M; Cacchiò G; Fabrizi GM; Scarcella M; Silvaggio F; Cavallaro T; Taioli F; Trojano L Neurol Sci; 2007 Aug; 28(4):181-4. PubMed ID: 17690848 [TBL] [Abstract][Full Text] [Related]
20. First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family. Valenti R; Bianchi S; Pescini F; D'Eramo C; Inzitari D; Dotti MT; Pantoni L J Neurol; 2011 Sep; 258(9):1632-6. PubMed ID: 21409506 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]