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 *

204 related articles for article (PubMed ID: 21414809)

  • 21. [The new diagnostic methods of CADASIL as differential diagnosis of HDLS].
    Ueda A; Ando Y
    Rinsho Shinkeigaku; 2014; 54(12):1168-70. PubMed ID: 25672735
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) presenting with stroke in a young man.
    Dunphy L; Rani A; Duodu Y; Behnam Y
    BMJ Case Rep; 2019 Jul; 12(7):. PubMed ID: 31324668
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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]  

  • 27. [Differential diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Moroz AA; Abramycheva NY; Stepanova MS; Konovalov RN; Timerbaeva SL; Illarioshkin SN
    Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(4):75-80. PubMed ID: 28617385
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanism.
    Cognat E; Baron-Menguy C; Domenga-Denier V; Cleophax S; Fouillade C; Monet-Leprêtre M; Dewerchin M; Joutel A
    Stroke; 2014 Mar; 45(3):842-9. PubMed ID: 24425116
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Childhood-onset CADASIL: clinical, imaging, and neurocognitive features.
    Hartley J; Westmacott R; Decker J; Shroff M; Yoon G
    J Child Neurol; 2010 May; 25(5):623-7. PubMed ID: 20197270
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. [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]  

  • 32. 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]  

  • 33. [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]  

  • 34. [CADASIL and CARASIL].
    López JI; Vilanova JR
    Neurologia; 2009 Mar; 24(2):125-30. PubMed ID: 19322691
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. [CADASIL: a case series of 11 patients].
    Vázquez do Campo R; Morales-Vidal S; Randolph C; Chadwick L; Biller J
    Rev Neurol; 2011 Feb; 52(4):202-10. PubMed ID: 21312166
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Identification of a novel NOTCH3 mutation in a family featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy].
    Zhu Y; Wang J; Wu Y; Wang G; Hu B; Xu A
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):578-81. PubMed ID: 25297585
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetically confirmed CADASIL in a pediatric patient.
    Cleves C; Friedman NR; Rothner AD; Hussain MS
    Pediatrics; 2010 Dec; 126(6):e1603-7. PubMed ID: 21078731
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A large number of cerebral microbleeds in CADASIL patients presenting with recurrent seizures: a case report.
    Anamnart C; Songsaeng D; Chanprasert S
    BMC Neurol; 2019 May; 19(1):106. PubMed ID: 31146726
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 11.