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Journal Abstract Search

953 related items for PubMed ID: 19539236

  • 21. [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
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. [Study of the familiar form of vascular dementia (CADASIL)].
    Takahashi K, Yoshizaki K.
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2007 Jun; 27(3):141-5. PubMed ID: 17633526
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  • 24. Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature.
    Joutel A.
    Bioessays; 2011 Jan; 33(1):73-80. PubMed ID: 20967782
    [Abstract] [Full Text] [Related]

  • 25. 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 15; 271(1-2):207-10. PubMed ID: 18499132
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  • 28. Notch3 Arg170Cys knock-in mice display pathologic and clinical features of the neurovascular disorder cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Wallays G, Nuyens D, Silasi-Mansat R, Souffreau J, Callaerts-Vegh Z, Van Nuffelen A, Moons L, D'Hooge R, Lupu F, Carmeliet P, Collen D, Dewerchin M.
    Arterioscler Thromb Vasc Biol; 2011 Dec 15; 31(12):2881-8. PubMed ID: 21940951
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  • 31. [Cerebral autosomal dominant arteriolopathy with subcortical infarcts and leucoencephalopathy].
    Bruls E, Moonen G, Sadzot B.
    Rev Med Liege; 2007 Jan 15; 62(1):36-43. PubMed ID: 17343128
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  • 33. 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 15; 36(8):2443.e1-7. PubMed ID: 26002683
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  • 34. 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 15; 27(10):1307-14. PubMed ID: 22936449
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  • 35. [Clinical features in 4 Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
    Lv H, Yao S, Zhang W, Wang ZX, Huang YN, Niu XY, Zhang Z, Yuan Y.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2004 Oct 15; 36(5):496-500. PubMed ID: 15489930
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  • 36. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome mutations increase susceptibility to spreading depression.
    Eikermann-Haerter K, Yuzawa I, Dilekoz E, Joutel A, Moskowitz MA, Ayata C.
    Ann Neurol; 2011 Feb 15; 69(2):413-8. PubMed ID: 21387384
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  • 37. 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 15; 11(1):19-29. PubMed ID: 15631641
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  • 38. Conventional MRI and NOTCH3 gene screening in sporadic CADASIL.
    Liguori M, Mazzei R, Ungaro C, Simone IL, Gambardella A, Plasmati I, Fera F, Aguglia U, Lanza P, Bono F, Chiumarulo L, Conforti FL, Consoli D, Quattrone A.
    Neurology; 2009 Feb 03; 72(5):469-71. PubMed ID: 19056668
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  • 39. CADASIL: experimental insights from animal models.
    Ayata C.
    Stroke; 2010 Oct 03; 41(10 Suppl):S129-34. PubMed ID: 20876488
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  • 40. Childhood-onset CADASIL: clinical, imaging, and neurocognitive features.
    Hartley J, Westmacott R, Decker J, Shroff M, Yoon G.
    J Child Neurol; 2010 May 03; 25(5):623-7. PubMed ID: 20197270
    [Abstract] [Full Text] [Related]

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