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407 related items for PubMed ID: 19174371

  • 1. 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; 132(Pt 4):933-9. PubMed ID: 19174371
    [Abstract] [Full Text] [Related]

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  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. Skin and sural nerve biopsies: ultrastructural findings in the first genetically confirmed cases of CADASIL in Serbia.
    Lackovic V, Bajcetic M, Lackovic M, Novakovic I, Labudović Borović M, Pavlovic A, Zidverc-Trajkovic J, Dzolic E, Rovcanin B, Sternic N, Kostic V.
    Ultrastruct Pathol; 2012 Oct; 36(5):325-35. PubMed ID: 23025651
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  • 5. Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASIL.
    Ishiko A, Shimizu A, Nagata E, Takahashi K, Tabira T, Suzuki N.
    Acta Neuropathol; 2006 Sep; 112(3):333-9. PubMed ID: 16871402
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  • 6. 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
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  • 7. Brain microvascular accumulation and distribution of the NOTCH3 ectodomain and granular osmiophilic material in CADASIL.
    Yamamoto Y, Craggs LJ, Watanabe A, Booth T, Attems J, Low RW, Oakley AE, Kalaria RN.
    J Neuropathol Exp Neurol; 2013 May; 72(5):416-31. PubMed ID: 23584202
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  • 8. 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]

  • 9. Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain.
    Monet-Leprêtre M, Bardot B, Lemaire B, Domenga V, Godin O, Dichgans M, Tournier-Lasserve E, Cohen-Tannoudji M, Chabriat H, Joutel A.
    Brain; 2009 Jun 15; 132(Pt 6):1601-12. PubMed ID: 19293235
    [Abstract] [Full Text] [Related]

  • 10. Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Kusaba T, Hatta T, Kimura T, Sonomura K, Tanda S, Kishimoto N, Kameyama H, Okigaki M, Mori Y, Ishigami N, Mizuno T, Nakagawa M, Matsubara H.
    Clin Nephrol; 2007 Mar 15; 67(3):182-7. PubMed ID: 17390743
    [Abstract] [Full Text] [Related]

  • 11. Ultrastructure of granular osmiophilic material deposits (GOM) in arterioles of CADASIL patients.
    Lewandowska E, Dziewulska D, Parys M, Pasennik E.
    Folia Neuropathol; 2011 Mar 15; 49(3):174-80. PubMed ID: 22101950
    [Abstract] [Full Text] [Related]

  • 12. Peripheral arteriopathy caused by Notch3 gain-of-function mutation involves ER and oxidative stress and blunting of NO/sGC/cGMP pathway.
    Neves KB, Morris HE, Alves-Lopes R, Muir KW, Moreton F, Delles C, Montezano AC, Touyz RM.
    Clin Sci (Lond); 2021 Mar 26; 135(6):753-773. PubMed ID: 33681964
    [Abstract] [Full Text] [Related]

  • 13. Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): report of a case with a six-year follow-up.
    Ragno M, Trojano L, Pianese L, Boni MV, Silvestri S, Mambelli V, Lorenzi T, Scarpelli M, Morroni M.
    Histol Histopathol; 2012 Oct 26; 27(10):1307-14. PubMed ID: 22936449
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  • 14. 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 Oct 26; 53(2):168-71. PubMed ID: 26216120
    [Abstract] [Full Text] [Related]

  • 15. [CADASIL].
    Uchino M.
    Brain Nerve; 2008 Nov 26; 60(11):1224-34. PubMed ID: 19069156
    [Abstract] [Full Text] [Related]

  • 16. Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Ruchoux MM, Domenga V, Brulin P, Maciazek J, Limol S, Tournier-Lasserve E, Joutel A.
    Am J Pathol; 2003 Jan 26; 162(1):329-42. PubMed ID: 12507916
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  • 17.
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  • 18. Novel Mutation of the NOTCH3 Gene in a Chinese Pedigree with CADASIL.
    Hou X, He C, Jin Q, Niu Q, Ren G, Cheng H.
    CNS Neurol Disord Drug Targets; 2017 Jan 26; 16(1):30-35. PubMed ID: 27781952
    [Abstract] [Full Text] [Related]

  • 19. New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).
    Abramycheva N, Stepanova M, Kalashnikova L, Zakharova M, Maximova M, Tanashyan M, Lagoda O, Fedotova E, Klyushnikov S, Konovalov R, Sakharova A, Illarioshkin S.
    J Neurol Sci; 2015 Feb 15; 349(1-2):196-201. PubMed ID: 25623805
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  • 20. Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.
    Santa Y, Uyama E, Chui DH, Arima M, Kotorii S, Takahashi K, Tabira T.
    J Neurol Sci; 2003 Aug 15; 212(1-2):79-84. PubMed ID: 12810003
    [Abstract] [Full Text] [Related]

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