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Journal Abstract Search

526 related items for PubMed ID: 21309761

  • 1. CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life.
    Melani F, Mei D, Pisano T, Savasta S, Franzoni E, Ferrari AR, Marini C, Guerrini R.
    Dev Med Child Neurol; 2011 Apr; 53(4):354-60. PubMed ID: 21309761
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  • 2. CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life.
    Arts WF.
    Dev Med Child Neurol; 2011 Apr; 53(4):296-7. PubMed ID: 21361914
    [No Abstract] [Full Text] [Related]

  • 3. Myoclonic encephalopathy in the CDKL5 gene mutation.
    Buoni S, Zannolli R, Colamaria V, Macucci F, di Bartolo RM, Corbini L, Orsi A, Zappella M, Hayek J.
    Clin Neurophysiol; 2006 Jan; 117(1):223-7. PubMed ID: 16326141
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  • 6. The three stages of epilepsy in patients with CDKL5 mutations.
    Bahi-Buisson N, Kaminska A, Boddaert N, Rio M, Afenjar A, Gérard M, Giuliano F, Motte J, Héron D, Morel MA, Plouin P, Richelme C, des Portes V, Dulac O, Philippe C, Chiron C, Nabbout R, Bienvenu T.
    Epilepsia; 2008 Jun; 49(6):1027-37. PubMed ID: 18266744
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  • 8. Seizures and electroencephalographic findings in CDKL5 mutations: case report and review.
    Grosso S, Brogna A, Bazzotti S, Renieri A, Morgese G, Balestri P.
    Brain Dev; 2007 May; 29(4):239-42. PubMed ID: 17049193
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  • 10. Clinical and electrographic features of epileptic spasms persisting beyond the second year of life.
    de Menezes MA, Rho JM.
    Epilepsia; 2002 Jun; 43(6):623-30. PubMed ID: 12060022
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  • 12. Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.
    Milh M, Villeneuve N, Chouchane M, Kaminska A, Laroche C, Barthez MA, Gitiaux C, Bartoli C, Borges-Correia A, Cacciagli P, Mignon-Ravix C, Cuberos H, Chabrol B, Villard L.
    Epilepsia; 2011 Oct; 52(10):1828-34. PubMed ID: 21770924
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  • 14. CDKL5-associated developmental and epileptic encephalopathy: A long-term, longitudinal electroclinical study of 22 cases.
    Darra F, Monchelato M, Loos M, Juanes M, Bernardina BD, Valenzuela GR, Gallo A, Caraballo R.
    Epilepsy Res; 2023 Feb; 190():107098. PubMed ID: 36739728
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  • 16. CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy.
    Nabbout R, Depienne C, Chipaux M, Girard B, Souville I, Trouillard O, Dulac O, Chelly J, Afenjar A, Héron D, Leguern E, Beldjord C, Bienvenu T, Bahi-Buisson N.
    Epilepsy Res; 2009 Nov; 87(1):25-30. PubMed ID: 19734009
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  • 17. First report of Tunisian patients with CDKL5-related encephalopathy.
    Charfi Triki C, Zouari Mallouli S, Ben Jdila M, Ben Said M, Kamoun Feki F, Weckhuysen S, Masmoudi S, Fakhfakh F.
    Epilepsia Open; 2024 Jun; 9(3):906-917. PubMed ID: 37701975
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  • 18. Historic, clinical, and prognostic features of epileptic encephalopathies caused by CDKL5 mutations.
    Moseley BD, Dhamija R, Wirrell EC, Nickels KC.
    Pediatr Neurol; 2012 Feb; 46(2):101-5. PubMed ID: 22264704
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