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Journal Abstract Search

249 related items for PubMed ID: 27781952

  • 1.
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    [No Abstract] [Full Text] [Related]

  • 2. A Novel Mutation Outside of the EGFr Encoding Exons of NOTCH3 Gene in a Chinese with CADASIL.
    Wang W, Ren Z, Shi Y, Zhang J.
    J Stroke Cerebrovasc Dis; 2020 Dec; 29(12):105410. PubMed ID: 33254371
    [Abstract] [Full Text] [Related]

  • 3. Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report.
    He R, Li H, Sun Y, Chen M, Wang L, Zhu Y, Zhang C.
    BMC Neurol; 2020 Mar 02; 20(1):72. PubMed ID: 32122318
    [Abstract] [Full Text] [Related]

  • 4. Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Tang SC, Lee MJ, Jeng JS, Yip PK.
    J Neurol Sci; 2005 Feb 15; 228(2):125-8. PubMed ID: 15694192
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 246(1-2):111-5. PubMed ID: 16580020
    [Abstract] [Full Text] [Related]

  • 6. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
    Ueda M, Nakaguma R, Ando Y.
    Rinsho Byori; 2009 Mar 15; 57(3):242-51. PubMed ID: 19363995
    [Abstract] [Full Text] [Related]

  • 7. Novel and Recurring NOTCH3 Mutations in Two Chinese Patients with CADASIL.
    Chen X, Deng S, Xu H, Hou D, Hu P, Yang Y, Wen J, Deng H, Yuan L.
    Neurodegener Dis; 2019 Mar 15; 19(1):35-42. PubMed ID: 31212292
    [Abstract] [Full Text] [Related]

  • 8. What factors determine phenotype of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)? Considerations in the context of a novel pathogenic R110C mutation in the NOTCH3 gene.
    Dziewulska D, Sulejczak D, Wężyk M.
    Folia Neuropathol; 2017 Mar 15; 55(4):295-300. PubMed ID: 29363903
    [Abstract] [Full Text] [Related]

  • 9. A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
    Algahtani H, Shirah B, Alharbi SY, Al-Qahtani MH, Abdulkareem AA, Naseer MI.
    J Stroke Cerebrovasc Dis; 2020 Jul 15; 29(7):104832. PubMed ID: 32414585
    [Abstract] [Full Text] [Related]

  • 10. A Chinese CADASIL Family with a Novel Mutation on Exon 10 of Notch3 Gene.
    Liu Y, Huang S, Yu L, Li T, Diao S, Chen Z, Zhou G, Sheng X, Xu Y, Fang Q.
    J Stroke Cerebrovasc Dis; 2021 Aug 15; 30(8):105674. PubMed ID: 34119749
    [Abstract] [Full Text] [Related]

  • 11. Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.
    Tikka S, Mykkänen K, Ruchoux MM, Bergholm R, Junna M, Pöyhönen M, Yki-Järvinen H, Joutel A, Viitanen M, Baumann M, Kalimo H.
    Brain; 2009 Apr 15; 132(Pt 4):933-9. PubMed ID: 19174371
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 258(9):1632-6. PubMed ID: 21409506
    [Abstract] [Full Text] [Related]

  • 13. A novel report of Cys1298Gly mutation in exon 24 of NOTCH3 gene in a Chinese family with CADASIL.
    Hu J, Qian J, Che Z, Tang B, Li Y, Gong Q, Lu X.
    J Stroke Cerebrovasc Dis; 2023 Aug 15; 32(8):107208. PubMed ID: 37295172
    [Abstract] [Full Text] [Related]

  • 14.
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  • 15. Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL.
    Dorszewska J, Kowalska M, Grzegorski T, Dziewulska D, Karmelita-Katulska K, Barciszewska AM, Prendecki M, Gorczyński W, Kozubski W.
    Folia Neuropathol; 2020 Aug 15; 58(1):83-92. PubMed ID: 32337960
    [Abstract] [Full Text] [Related]

  • 16.
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  • 17. Are granular osmiophilic material deposits an epiphenomenon in CADASIL?
    Erro R, Moccia M, Cervasio M, Penco S, De Caro Mdel B, Barone P.
    Folia Neuropathol; 2015 Aug 15; 53(2):168-71. PubMed ID: 26216120
    [Abstract] [Full Text] [Related]

  • 18. A Chinese CADASIL family with p.R578C mutation at exon 11 of the NOTCH3 gene.
    Wu X, Zhang A, Li Y, Lei X, Guo S, Tian T, Gong H, He D.
    Clin Neurol Neurosurg; 2021 Sep 15; 208():106833. PubMed ID: 34352628
    [Abstract] [Full Text] [Related]

  • 19. Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese.
    Lee YC, Liu CS, Chang MH, Lin KP, Fuh JL, Lu YC, Liu YF, Soong BW.
    J Neurol; 2009 Feb 15; 256(2):249-55. PubMed ID: 19242647
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 267(1-2):170-3. PubMed ID: 18022198
    [Abstract] [Full Text] [Related]

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