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Journal Abstract Search

270 related items for PubMed ID: 20728410

  • 1. Epilepsy in Rett syndrome: clinical and genetic features.
    Pintaudi M, Calevo MG, Vignoli A, Parodi E, Aiello F, Baglietto MG, Hayek Y, Buoni S, Renieri A, Russo S, Cogliati F, Giordano L, Canevini M, Veneselli E.
    Epilepsy Behav; 2010 Nov; 19(3):296-300. PubMed ID: 20728410
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  • 2. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
    Buoni S, Zannolli R, Felice CD, Saponari S, Strambi M, Dotti MT, Castrucci E, Corbini L, Orsi A, Hayek J.
    Clin Neurophysiol; 2008 Nov; 119(11):2455-8. PubMed ID: 18842453
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  • 3. Epilepsy in Rett syndrome---the experience of a National Rett Center.
    Nissenkorn A, Gak E, Vecsler M, Reznik H, Menascu S, Ben Zeev B.
    Epilepsia; 2010 Jul; 51(7):1252-8. PubMed ID: 20491871
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  • 4. Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature.
    Pintaudi M, Baglietto MG, Gaggero R, Parodi E, Pessagno A, Marchi M, Russo S, Veneselli E.
    Epilepsy Behav; 2008 Feb; 12(2):326-31. PubMed ID: 18063413
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  • 5. Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
    Hadzsiev K, Polgar N, Bene J, Komlosi K, Karteszi J, Hollody K, Kosztolanyi G, Renieri A, Melegh B.
    J Hum Genet; 2011 Mar; 56(3):183-7. PubMed ID: 21160487
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  • 7. A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder.
    Psoni S, Willems PJ, Kanavakis E, Mavrou A, Frissyra H, Traeger-Synodinos J, Sofokleous C, Makrythanassis P, Kitsiou-Tzeli S.
    Eur J Paediatr Neurol; 2010 Mar; 14(2):188-91. PubMed ID: 19428276
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  • 8. Epilepsy in Rett syndrome--lessons from the Rett networked database.
    Nissenkorn A, Levy-Drummer RS, Bondi O, Renieri A, Villard L, Mari F, Mencarelli MA, Lo Rizzo C, Meloni I, Pineda M, Armstrong J, Clarke A, Bahi-Buisson N, Mejaski BV, Djuric M, Craiu D, Djukic A, Pini G, Bisgaard AM, Melegh B, Vignoli A, Russo S, Anghelescu C, Veneselli E, Hayek J, Ben-Zeev B.
    Epilepsia; 2015 Apr; 56(4):569-76. PubMed ID: 25789914
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  • 12. Epilepsy treatment in Rett syndrome.
    Krajnc N, Župančič N, Oražem J.
    J Child Neurol; 2011 Nov; 26(11):1429-33. PubMed ID: 21636780
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  • 13. Early onset seizures and Rett-like features associated with mutations in CDKL5.
    Evans JC, Archer HL, Colley JP, Ravn K, Nielsen JB, Kerr A, Williams E, Christodoulou J, Gécz J, Jardine PE, Wright MJ, Pilz DT, Lazarou L, Cooper DN, Sampson JR, Butler R, Whatley SD, Clarke AJ.
    Eur J Hum Genet; 2005 Oct; 13(10):1113-20. PubMed ID: 16015284
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  • 16. Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients.
    Santos M, Temudo T, Kay T, Carrilho I, Medeira A, Cabral H, Gomes R, Lourenço MT, Venâncio M, Calado E, Moreira A, Oliveira G, Maciel P.
    J Child Neurol; 2009 Jan; 24(1):49-55. PubMed ID: 19168818
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  • 20. Clinical and genetic Rett syndrome variants are defined by stable electrophysiological profiles.
    Keogh C, Pini G, Dyer AH, Bigoni S, DiMarco P, Gemo I, Reilly R, Tropea D.
    BMC Pediatr; 2018 Oct 19; 18(1):333. PubMed ID: 30340473
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