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Journal Abstract Search

382 related items for PubMed ID: 27143072

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  • 3. The clinical spectrum of female epilepsy patients with PCDH19 mutations in a Chinese population.
    Liu A, Xu X, Yang X, Jiang Y, Yang Z, Liu X, Wu Y, Wu X, Wei L, Zhang Y.
    Clin Genet; 2017 Jan; 91(1):54-62. PubMed ID: 27527380
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  • 5. Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome.
    Kwong AK, Fung CW, Chan SY, Wong VC.
    PLoS One; 2012 Jan; 7(7):e41802. PubMed ID: 22848613
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  • 8. [Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy].
    Zhang YH, Sun HH, Liu XY, Ma XW, Yang ZX, Xiong H, Qin J, Lin Q, Wu XR.
    Zhonghua Er Ke Za Zhi; 2008 Oct; 46(10):769-73. PubMed ID: 19099883
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  • 13. Dravet syndrome: a genetic epileptic disorder.
    Akiyama M, Kobayashi K, Ohtsuka Y.
    Acta Med Okayama; 2012 Oct; 66(5):369-76. PubMed ID: 23093055
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  • 15. Early and long-term electroclinical features of patients with epilepsy and PCDH19 mutation.
    Chemaly N, Losito E, Pinard JM, Gautier A, Villeneuve N, Arbues AS, An I, Desguerre I, Dulac O, Chiron C, Kaminska A, Nabbout R.
    Epileptic Disord; 2018 Dec 01; 20(6):457-467. PubMed ID: 30530412
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  • 16. PCDH19-related female-limited epilepsy: further details regarding early clinical features and therapeutic efficacy.
    Higurashi N, Nakamura M, Sugai M, Ohfu M, Sakauchi M, Sugawara Y, Nakamura K, Kato M, Usui D, Mogami Y, Fujiwara Y, Ito T, Ikeda H, Imai K, Takahashi Y, Nukui M, Inoue T, Okazaki S, Kirino T, Tomonoh Y, Inoue T, Takano K, Shimakawa S, Hirose S.
    Epilepsy Res; 2013 Sep 01; 106(1-2):191-9. PubMed ID: 23712037
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  • 17. [Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome].
    Xu XJ, Zhang YH, Sun HH, Liu XY, Jiang YW, Wu XR.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec 01; 29(6):625-30. PubMed ID: 23225037
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  • 19. Protocadherin 19 mutations in girls with infantile-onset epilepsy.
    Marini C, Mei D, Parmeggiani L, Norci V, Calado E, Ferrari A, Moreira A, Pisano T, Specchio N, Vigevano F, Battaglia D, Guerrini R.
    Neurology; 2010 Aug 17; 75(7):646-53. PubMed ID: 20713952
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