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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 15776792)

  • 1. Early diagnosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): the role of MRI.
    Fattapposta F; Restuccia R; Pirro C; Malandrini A; Locuratolo N; Amabile G; Bianco F
    Funct Neurol; 2004; 19(4):239-42. PubMed ID: 15776792
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Lesnik Oberstein SA; Haan J
    Panminerva Med; 2004 Dec; 46(4):265-76. PubMed ID: 15876982
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Cerebral autosomal dominant arteriolopathy with subcortical infarcts and leucoencephalopathy].
    Bruls E; Moonen G; Sadzot B
    Rev Med Liege; 2007 Jan; 62(1):36-43. PubMed ID: 17343128
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The spectrum of mutations for CADASIL diagnosis.
    Federico A; Bianchi S; Dotti MT
    Neurol Sci; 2005 Jun; 26(2):117-24. PubMed ID: 15995828
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Characteristics of CADASIL in Korea: a novel cysteine-sparing Notch3 mutation.
    Kim Y; Choi EJ; Choi CG; Kim G; Choi JH; Yoo HW; Kim JS
    Neurology; 2006 May; 66(10):1511-6. PubMed ID: 16717210
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. [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]  

  • 10. CADASIL.
    Hervé D; Chabriat H
    J Geriatr Psychiatry Neurol; 2010 Dec; 23(4):269-76. PubMed ID: 21045164
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy without anterior temporal pole involvement: a case report.
    Kobayashi J; Sato S; Okumura K; Miyashita F; Ueda A; Ando Y; Toyoda K
    J Stroke Cerebrovasc Dis; 2014 Mar; 23(3):e241-2. PubMed ID: 24295602
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. CADASIL can mimic multiple sclerosis.
    Phillips CD; Zuckerman SJ;
    J La State Med Soc; 2010; 162(3):174. PubMed ID: 20666172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetically proven cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a 3-year-old.
    Benabu Y; Beland M; Ferguson N; Maranda B; Boucher RM
    Pediatr Radiol; 2013 Sep; 43(9):1227-30. PubMed ID: 23460375
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
    Chen YC; Hsiao CT; Soong BW; Lee YC
    Acta Neurol Taiwan; 2014 Jun; 23(2):64-74. PubMed ID: 26035923
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.
    Joutel A; Corpechot C; Ducros A; Vahedi K; Chabriat H; Mouton P; Alamowitch S; Domenga V; Cécillion M; Maréchal E; Maciazek J; Vayssière C; Cruaud C; Cabanis EA; Ruchoux MM; Weissenbach J; Bach JF; Bousser MG; Tournier-Lasserve E
    Ann N Y Acad Sci; 1997 Sep; 826():213-7. PubMed ID: 9329692
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lacunar infarcts are the main correlate with cognitive dysfunction in CADASIL.
    Liem MK; van der Grond J; Haan J; van den Boom R; Ferrari MD; Knaap YM; Breuning MH; van Buchem MA; Middelkoop HA; Lesnik Oberstein SA
    Stroke; 2007 Mar; 38(3):923-8. PubMed ID: 17272761
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Associated With a Novel In-Frame Mutation in the NOTCH3 Gene in a Japanese Patient.
    Takeshi Y; Suda S; Shimoyama T; Aoki J; Suzuki K; Okubo S; Mizuta I; Mizuno T; Kimura K
    J Stroke Cerebrovasc Dis; 2020 Jan; 29(1):104482. PubMed ID: 31699577
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Case of CADASIL showing spontaneous subcortical hemorrhage with a novel mutation of Notch3 gene].
    Kotorii S; Goto H; Kondo T; Matsuo H; Takahashi K; Shibuya N
    Rinsho Shinkeigaku; 2006 Sep; 46(9):644-8. PubMed ID: 17260807
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.