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Journal Abstract Search

424 related items for PubMed ID: 18035376

  • 1. Identification of an Arg35X mutation in the PDCD10 gene in a patient with cerebral and multiple spinal cavernous malformations.
    Lee ST, Choi KW, Yeo HT, Kim JW, Ki CS, Cho YD.
    J Neurol Sci; 2008 Apr 15; 267(1-2):177-81. PubMed ID: 18035376
    [Abstract] [Full Text] [Related]

  • 2. CCM3 mutations are uncommon in cerebral cavernous malformations.
    Verlaan DJ, Roussel J, Laurent SB, Elger CE, Siegel AM, Rouleau GA.
    Neurology; 2005 Dec 27; 65(12):1982-3. PubMed ID: 16380626
    [Abstract] [Full Text] [Related]

  • 3. A novel KRIT1 gene mutation in a patient with cerebral and multiple spinal cavernous malformations.
    Lee YW, Lee ST, Cha JG, Park JH, Jeon BR, Lee YK, Kim JW, Ki CS.
    Ann Clin Lab Sci; 2010 Dec 27; 40(3):290-4. PubMed ID: 20689144
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  • 4. 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; 27(1):118. PubMed ID: 16329096
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  • 5. Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations.
    Labauge P, Fontaine B, Neau JP, Bergametti F, Riant F, Blecon A, Marchelli F, Arnoult M, Lannuzel A, Clanet M, Olschwang S, Denier C, Tournier-Lasserve E.
    Neurology; 2009 Jun 09; 72(23):2044-6. PubMed ID: 19506228
    [No Abstract] [Full Text] [Related]

  • 6. 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 09; 29(5):709-17. PubMed ID: 18300272
    [Abstract] [Full Text] [Related]

  • 7. Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.
    Battistini S, Rocchi R, Cerase A, Citterio A, Tassi L, Lando G, Patrosso MC, Galli R, Brunori P, Sgrò DL, Pitillo G, Lo Russo G, Marocchi A, Penco S.
    Arch Neurol; 2007 Jun 09; 64(6):843-8. PubMed ID: 17562932
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  • 9. Clinical features of cerebral cavernous malformations patients with KRIT1 mutations.
    Denier C, Labauge P, Brunereau L, Cavé-Riant F, Marchelli F, Arnoult M, Cecillon M, Maciazek J, Joutel A, Tournier-Lasserve E, Sociéte Française de Neurochirgurgie, Sociéte de Neurochirurgie de Langue Française.
    Ann Neurol; 2004 Feb 09; 55(2):213-20. PubMed ID: 14755725
    [Abstract] [Full Text] [Related]

  • 10. Identification of a c.601C>G mutation in the CCM1 gene in a kindred with multiple skin, spinal and cerebral cavernous malformations.
    Haghighi A, Fathi D, Shahbazi M, Motahari MM, Friedman B.
    J Neurol Sci; 2013 Nov 15; 334(1-2):97-101. PubMed ID: 24007869
    [Abstract] [Full Text] [Related]

  • 11. Recent insights into cerebral cavernous malformations: the molecular genetics of CCM.
    Riant F, Bergametti F, Ayrignac X, Boulday G, Tournier-Lasserve E.
    FEBS J; 2010 Mar 15; 277(5):1070-5. PubMed ID: 20096038
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  • 14. Spectrum of genotype and clinical manifestations in cerebral cavernous malformations.
    Gault J, Sain S, Hu LJ, Awad IA.
    Neurosurgery; 2006 Dec 15; 59(6):1278-84; discussion 1284-5. PubMed ID: 17277691
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  • 15. Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations.
    Cavé-Riant F, Denier C, Labauge P, Cécillon M, Maciazek J, Joutel A, Laberge-Le Couteulx S, Tournier-Lasserve E.
    Eur J Hum Genet; 2002 Nov 15; 10(11):733-40. PubMed ID: 12404106
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  • 17. PDCD10 gene mutations in multiple cerebral cavernous malformations.
    Cigoli MS, Avemaria F, De Benedetti S, Gesu GP, Accorsi LG, Parmigiani S, Corona MF, Capra V, Mosca A, Giovannini S, Notturno F, Ciccocioppo F, Volpi L, Estienne M, De Michele G, Antenora A, Bilo L, Tavoni A, Zamponi N, Alfei E, Baranello G, Riva D, Penco S.
    PLoS One; 2014 Nov 15; 9(10):e110438. PubMed ID: 25354366
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  • 18. Variable expression of cerebral cavernous malformations in carriers of a premature termination codon in exon 17 of the Krit1 gene.
    Lucas M, Costa AF, García-Moreno JM, Solano F, Gamero MA, Izquierdo G.
    BMC Neurol; 2003 Jul 23; 3():5. PubMed ID: 12877753
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  • 20. 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 23; 29(3):E1. PubMed ID: 20809750
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