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Journal Abstract Search

119 related items for PubMed ID: 19199464

  • 1. Molecular screening test in familial forms of cerebral cavernous malformation: the impact of the Multiplex Ligation-dependent Probe Amplification approach.
    Penco S, Ratti R, Bianchi E, Citterio A, Patrosso MC, Marocchi A, Tassi L, La Camera A, Collice M.
    J Neurosurg; 2009 May; 110(5):929-34. PubMed ID: 19199464
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  • 5. Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.
    Scimone C, Bramanti P, Alafaci C, Granata F, Piva F, Rinaldi C, Donato L, Greco F, Sidoti A, D'Angelo R.
    J Mol Neurosci; 2017 Feb; 61(2):189-198. PubMed ID: 28000143
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  • 9. High-throughput sequencing of the entire genomic regions of CCM1/KRIT1, CCM2 and CCM3/PDCD10 to search for pathogenic deep-intronic splice mutations in cerebral cavernous malformations.
    Rath M, Jenssen SE, Schwefel K, Spiegler S, Kleimeier D, Sperling C, Kaderali L, Felbor U.
    Eur J Med Genet; 2017 Sep; 60(9):479-484. PubMed ID: 28645800
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  • 10. Familial cerebral cavernous angiomas: clinical and genetic features in a Chinese family with a frame-shift mutation in the CCM1 gene (krit1).
    Zhu H, Guo Y, Feng X, Zhang R, Zhou C, Li G, Liu J.
    J Mol Neurosci; 2014 Dec; 54(4):790-5. PubMed ID: 25185960
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  • 11. Mutation analysis of CCM1, CCM2 and CCM3 genes in a cohort of Italian patients with cerebral cavernous malformation.
    D'Angelo R, Marini V, Rinaldi C, Origone P, Dorcaratto A, Avolio M, Goitre L, Forni M, Capra V, Alafaci C, Mareni C, Garrè C, Bramanti P, Sidoti A, Retta SF, Amato A.
    Brain Pathol; 2011 Mar; 21(2):215-24. PubMed ID: 21029238
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  • 12. Deletions in CCM2 are a common cause of cerebral cavernous malformations.
    Liquori CL, Berg MJ, Squitieri F, Leedom TP, Ptacek L, Johnson EW, Marchuk DA.
    Am J Hum Genet; 2007 Jan; 80(1):69-75. PubMed ID: 17160895
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  • 14. [Gene mutations in patients with hereditary cavernous malformations].
    Belousova OB, Bulygina ES, Okishev DN, Prohorchuk EB, Tsygankova SV, Pronin IN, Shishkina LV, Ryzhova MV, Skryabin KG, Konovalov AN.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2017 Jan; 117(6):66-72. PubMed ID: 28745674
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  • 16. 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 Jan; 9(10):e110438. PubMed ID: 25354366
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  • 17. A Novel KRIT1/CCM1 Gene Insertion Mutation Associated with Cerebral Cavernous Malformations in a Chinese Family.
    Wang H, Pan Y, Zhang Z, Li X, Xu Z, Suo Y, Li W, Wang Y.
    J Mol Neurosci; 2017 Feb; 61(2):221-226. PubMed ID: 28160210
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  • 18. Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
    Scimone C, Bramanti P, Ruggeri A, Katsarou Z, Donato L, Sidoti A, D'Angelo R.
    J Mol Neurosci; 2015 Nov; 57(3):400-3. PubMed ID: 26115622
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  • 19. CCM1 gene deletion identified by MLPA in cerebral cavernous malformation.
    Gaetzner S, Stahl S, Sürücü O, Schaafhausen A, Halliger-Keller B, Bertalanffy H, Sure U, Felbor U.
    Neurosurg Rev; 2007 Apr; 30(2):155-9; discussion 159-60. PubMed ID: 17187287
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  • 20. 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; 64(6):843-8. PubMed ID: 17562932
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