BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 22893421)

  • 1. [Imaging findings in autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) - CADASIL - the most frequent familial stroke syndrome].
    Bender B; Bornemann A; Reimold M; Ernemann U; Horger M
    Rofo; 2012 Aug; 184(8):679-83. PubMed ID: 22893421
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. An unusual case of elderly-onset cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with multiple cerebrovascular risk factors.
    Watanabe M; Adachi Y; Jackson M; Yamamoto-Watanabe Y; Wakasaya Y; Shirahama I; Takamura A; Matsubara E; Kawarabayashi T; Shoji M
    J Stroke Cerebrovasc Dis; 2012 Feb; 21(2):143-5. PubMed ID: 20851625
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CADASIL with a novel NOTCH3 mutation (Cys478Tyr).
    Ozaki K; Irioka T; Ishikawa K; Mizusawa H
    J Stroke Cerebrovasc Dis; 2015 Mar; 24(3):e61-2. PubMed ID: 25595846
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in two siblings with neuropsychiatric symptoms.
    Dericioglu N; Vural A; Agayeva N; Basar K; Anil Yagcioglu AE; Gursoy-Ozdemir Y
    Psychosomatics; 2013; 54(6):594-8. PubMed ID: 23414846
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. [CADASIL syndrome - cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Dziewulska D; Kwieciński H
    Neurol Neurochir Pol; 2008; 42(2):123-30. PubMed ID: 18512169
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Acute headache followed by focal neuropsychological impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Ducray F; Ritzenthaler T; Cho TH; Bruyas A; Cotton F; Cartalat-Carel S; Honnorat J; Nighoghossian N
    J Stroke Cerebrovasc Dis; 2010 Jan; 19(1):75-6. PubMed ID: 20123231
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis.
    Milunsky A; Konialis C; Shim SH; Maher TA; Spengos K; Ito M; Pangalos C
    Prenat Diagn; 2005 Nov; 25(11):1057-8. PubMed ID: 16302168
    [TBL] [Abstract][Full Text] [Related]  

  • 13. NOTCH3 variants in patients with subcortical vascular cognitive impairment: a comparison with typical CADASIL patients.
    Yoon CW; Kim YE; Seo SW; Ki CS; Choi SH; Kim JW; Na DL
    Neurobiol Aging; 2015 Aug; 36(8):2443.e1-7. PubMed ID: 26002683
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. Epilepsy in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Haan J; Lesnik Oberstein SA; Ferrari MD
    Cerebrovasc Dis; 2007; 24(2-3):316-7. PubMed ID: 17675836
    [No Abstract]   [Full Text] [Related]  

  • 17. Report of two Chinese families and a review of Mainland Chinese CADASIL patients.
    Yin XZ; Ding MP; Zhang BR; Liu JR; Zhang L; Wang PZ; Zhou FY; Zhao GH
    J Neurol Sci; 2009 Apr; 279(1-2):88-92. PubMed ID: 19167727
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Cadasil and other hereditary small vessel diseases of the brain--increasingly diagnosed conditions underlying familial ischaemic stroke and dementia].
    Gunda B; Chabriat H; Bereczki D
    Ideggyogy Sz; 2011 Mar; 64(3-4):88-100. PubMed ID: 21545006
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Chabriat H; Bousser MG
    Handb Clin Neurol; 2008; 89():671-86. PubMed ID: 18631787
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.