BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

360 related articles for article (PubMed ID: 19350513)

  • 1. [The clinical and genetic studies in a family of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Zhang LF; Yang XS; Wang YF; Pei LT
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):187-90. PubMed ID: 19350513
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [A study of subcortical infarcts and leukoencephalopathy (CADASIL) in a family with autosomal cerebral dominant arteriopathy].
    Jin DX; Chen XY; Zhang X
    Zhonghua Nei Ke Za Zhi; 2004 Dec; 43(12):924-7. PubMed ID: 15730739
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a Greek family.
    Mandellos D; Limbitaki G; Papadimitriou A; Anastasopoulos D
    Neurol Sci; 2005 Oct; 26(4):278-81. PubMed ID: 16193256
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy pedigree: clinical pathology, neuroimaging and molecular genetics studies].
    Chang MZ; Wang XL; Di ZL; Zhang L; Zhang WP; Li Q; Mao J; Qin AJ; Tian Y; Chen HL
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2011 Nov; 42(6):866-9. PubMed ID: 22332560
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Migraine and cerebral white matter lesions: when to suspect cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Gladstone JP; Dodick DW
    Neurologist; 2005 Jan; 11(1):19-29. PubMed ID: 15631641
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. [Cerebral arteriopathy with subcortical infarctions and leukoencephalopathy with dominant autosomal inheritance (CADASIL). Clinical and morphological study].
    Marrero Falcón C; Díez Tejedor E; Arpa Gutiérrez J; Barreiro Tella P
    Neurologia; 1999; 14(6):275-82. PubMed ID: 10439621
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL.
    Viswanathan A; Gschwendtner A; Guichard JP; Buffon F; Cumurciuc R; O'Sullivan M; Holtmannspötter M; Pachai C; Bousser MG; Dichgans M; Chabriat H
    Neurology; 2007 Jul; 69(2):172-9. PubMed ID: 17620550
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): a case report with review of literature.
    Gurumukhani JK; Ursekar M; Singhal BS
    Neurol India; 2004 Mar; 52(1):99-101. PubMed ID: 15069251
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Pathomechanisms and treatment of CADASIL].
    Mizuno T
    Brain Nerve; 2013 Jul; 65(7):811-23. PubMed ID: 23832984
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. [CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging].
    Chabriat H; Joutel A; Vahedi K; Iba-Zizen MT; Tournier-Lasserve E; Bousser MG
    Bull Acad Natl Med; 2000; 184(7):1523-31; discussion 1531-3. PubMed ID: 11261256
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 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. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs.
    Bohlega SA; Abu-Amero KK
    Saudi Med J; 2008 Jul; 29(7):952-6. PubMed ID: 18626519
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 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 18.