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Journal Abstract Search

357 related items for PubMed ID: 24796722

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  • 2. Myoclonus in Angelman syndrome.
    Pollack SF, Grocott OR, Parkin KA, Larson AM, Thibert RL.
    Epilepsy Behav; 2018 May; 82():170-174. PubMed ID: 29555100
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  • 4. Angelman Syndrome Due to UBE3A Gene Mutation.
    Goswami JN, Sahu JK, Singhi P.
    Indian J Pediatr; 2018 May; 85(5):390-391. PubMed ID: 29250725
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  • 5. Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy.
    Nicita F, Garone G, Papetti L, Consoli F, Magliozzi M, De Luca A, Spalice A.
    J Neurogenet; 2015 May; 29(4):178-82. PubMed ID: 26559560
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  • 6. Cortical myoclonus in Angelman syndrome.
    Guerrini R, De Lorey TM, Bonanni P, Moncla A, Dravet C, Suisse G, Livet MO, Bureau M, Malzac P, Genton P, Thomas P, Sartucci F, Simi P, Serratosa JM.
    Ann Neurol; 1996 Jul; 40(1):39-48. PubMed ID: 8687190
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  • 7. Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms.
    Guerrini R, Carrozzo R, Rinaldi R, Bonanni P.
    Paediatr Drugs; 2003 Jul; 5(10):647-61. PubMed ID: 14510623
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  • 13. Angelman syndrome due to a termination codon mutation of the UBE3A gene.
    Al-Maawali A, Machado J, Fang P, Dupuis L, Faghfoury H, Mendoza-Londono R.
    J Child Neurol; 2013 Mar; 28(3):392-5. PubMed ID: 22566713
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  • 14. Angelman syndrome: correlations between epilepsy phenotypes and genotypes.
    Minassian BA, DeLorey TM, Olsen RW, Philippart M, Bronstein Y, Zhang Q, Guerrini R, Van Ness P, Livet MO, Delgado-Escueta AV.
    Ann Neurol; 1998 Apr; 43(4):485-93. PubMed ID: 9546330
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  • 15. Novel human pathological mutations. Gene symbol: UBE3A. Disease: Angelman Syndrome.
    Tzagkaraki E, Christalena S, Helen F, Argyris D, Ariadni M, Emmanuel K.
    Hum Genet; 2009 Aug; 126(2):331. PubMed ID: 19693993
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  • 16. From electrophysiology to chromatin: a bottom-up approach to Angelman syndrome.
    Dan B, Servais L, Boyd SG, Wagstaff J, Cheron G.
    Ann N Y Acad Sci; 2004 Dec; 1030():599-611. PubMed ID: 15659843
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  • 17. Molecular and clinical characterization of Angelman syndrome in Chinese patients.
    Bai JL, Qu YJ, Jin YW, Wang H, Yang YL, Jiang YW, Yang XY, Zou LP, Song F.
    Clin Genet; 2014 Mar; 85(3):273-7. PubMed ID: 23551092
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  • 18. Mutation Update for UBE3A variants in Angelman syndrome.
    Sadikovic B, Fernandes P, Zhang VW, Ward PA, Miloslavskaya I, Rhead W, Rosenbaum R, Gin R, Roa B, Fang P.
    Hum Mutat; 2014 Dec; 35(12):1407-17. PubMed ID: 25212744
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