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Journal Abstract Search


140 related items for PubMed ID: 22776801

  • 1. Ultrastructural analysis of vascular features in cerebral cavernous malformations.
    Tanriover G, Sozen B, Seker A, Kilic T, Gunel M, Demir N.
    Clin Neurol Neurosurg; 2013 Apr; 115(4):438-44. PubMed ID: 22776801
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  • 2. Differential angiogenesis function of CCM2 and CCM3 in cerebral cavernous malformations.
    Zhu Y, Wu Q, Xu JF, Miller D, Sandalcioglu IE, Zhang JM, Sure U.
    Neurosurg Focus; 2010 Sep; 29(3):E1. PubMed ID: 20809750
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  • 3. Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex.
    Stahl S, Gaetzner S, Voss K, Brackertz B, Schleider E, Sürücü O, Kunze E, Netzer C, Korenke C, Finckh U, Habek M, Poljakovic Z, Elbracht M, Rudnik-Schöneborn S, Bertalanffy H, Sure U, Felbor U.
    Hum Mutat; 2008 May; 29(5):709-17. PubMed ID: 18300272
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  • 4. Cerebral Cavernous Malformation-1 Protein Controls DLL4-Notch3 Signaling Between the Endothelium and Pericytes.
    Schulz GB, Wieland E, Wüstehube-Lausch J, Boulday G, Moll I, Tournier-Lasserve E, Fischer A.
    Stroke; 2015 May; 46(5):1337-43. PubMed ID: 25791711
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  • 5. Cerebral cavernous malformations: from CCM genes to endothelial cell homeostasis.
    Fischer A, Zalvide J, Faurobert E, Albiges-Rizo C, Tournier-Lasserve E.
    Trends Mol Med; 2013 May; 19(5):302-8. PubMed ID: 23506982
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  • 7. Cerebral venous malformations have distinct genetic origin from cerebral cavernous malformations.
    Guclu B, Ozturk AK, Pricola KL, Seker A, Ozek M, Gunel M.
    Stroke; 2005 Nov; 36(11):2479-80. PubMed ID: 16239636
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  • 8. In vitro characterization of the angiogenic phenotype and genotype of the endothelia derived from sporadic cerebral cavernous malformations.
    Zhu Y, Wu Q, Fass M, Xu JF, You C, Müller O, Sandalcioglu IE, Zhang JM, Sure U.
    Neurosurgery; 2011 Sep; 69(3):722-31; discussion 731-2. PubMed ID: 21471841
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  • 11. Ultrastructural pathological features of cerebrovascular malformations: a preliminary report.
    Wong JH, Awad IA, Kim JH.
    Neurosurgery; 2000 Jun; 46(6):1454-9. PubMed ID: 10834648
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  • 12. Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus.
    Liquori CL, Berg MJ, Squitieri F, Ottenbacher M, Sorlie M, Leedom TP, Cannella M, Maglione V, Ptacek L, Johnson EW, Marchuk DA.
    Hum Mutat; 2006 Jan; 27(1):118. PubMed ID: 16329096
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  • 16. Cerebral cavernous malformations as a disease of vascular permeability: from bench to bedside with caution.
    Yadla S, Jabbour PM, Shenkar R, Shi C, Campbell PG, Awad IA.
    Neurosurg Focus; 2010 Sep; 29(3):E4. PubMed ID: 20809762
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  • 17. Genetics of cerebral cavernous malformations.
    Plummer NW, Zawistowski JS, Marchuk DA.
    Curr Neurol Neurosci Rep; 2005 Sep; 5(5):391-6. PubMed ID: 16131422
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  • 18. Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathology.
    Louvi A, Chen L, Two AM, Zhang H, Min W, Günel M.
    Proc Natl Acad Sci U S A; 2011 Mar 01; 108(9):3737-42. PubMed ID: 21321212
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