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Journal Abstract Search

554 related items for PubMed ID: 16495142

  • 1.
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  • 2. Epilepsy in patients with angelman syndrome caused by deletion of the chromosome 15q11-13.
    Valente KD, Koiffmann CP, Fridman C, Varella M, Kok F, Andrade JQ, Grossmann RM, Marques-Dias MJ.
    Arch Neurol; 2006 Jan; 63(1):122-8. PubMed ID: 16401744
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  • 3. Spectrum of epilepsy in terminal 1p36 deletion syndrome.
    Bahi-Buisson N, Guttierrez-Delicado E, Soufflet C, Rio M, Daire VC, Lacombe D, Héron D, Verloes A, Zuberi S, Burglen L, Afenjar A, Moutard ML, Edery P, Novelli A, Bernardini L, Dulac O, Nabbout R, Plouin P, Battaglia A.
    Epilepsia; 2008 Mar; 49(3):509-15. PubMed ID: 18031548
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  • 5. Successful surgery for epilepsy due to early brain lesions despite generalized EEG findings.
    Wyllie E, Lachhwani DK, Gupta A, Chirla A, Cosmo G, Worley S, Kotagal P, Ruggieri P, Bingaman WE.
    Neurology; 2007 Jul 24; 69(4):389-97. PubMed ID: 17646632
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  • 6. Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome.
    Galván-Manso M, Campistol J, Conill J, Sanmartí FX.
    Epileptic Disord; 2005 Mar 24; 7(1):19-25. PubMed ID: 15741136
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  • 8. Pattern-sensitive epilepsy: electroclinical characteristics, natural history, and delineation of the epileptic syndrome.
    Radhakrishnan K, St Louis EK, Johnson JA, McClelland RL, Westmoreland BF, Klass DW.
    Epilepsia; 2005 Jan 24; 46(1):48-58. PubMed ID: 15660768
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  • 9. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.
    Battaglia A.
    Brain Dev; 2005 Aug 24; 27(5):365-9. PubMed ID: 16023554
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  • 10. Rearrangements of chromosome 15 in epilepsy.
    Torrisi L, Sangiorgi E, Russo L, Gurrieri F.
    Am J Med Genet; 2001 Aug 24; 106(2):125-8. PubMed ID: 11579432
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  • 13. Idiopathic epilepsy with generalized tonic-clonic seizures only versus idiopathic epilepsy with phantom absences and generalized tonic-clonic seizures: one or two syndromes?
    Koutroumanidis M, Aggelakis K, Panayiotopoulos CP.
    Epilepsia; 2008 Dec 24; 49(12):2050-62. PubMed ID: 18616555
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  • 18. Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case report.
    Kraoua L, Chaabouni M, Ewers E, Chelly I, Ouertani I, Ben Jemaa L, Maazoul F, Liehr T, Chaabouni H.
    Eur J Med Genet; 2011 Dec 24; 54(4):e446-50. PubMed ID: 21621018
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  • 19. Epilepsy and mental retardation limited to females: an under-recognized disorder.
    Scheffer IE, Turner SJ, Dibbens LM, Bayly MA, Friend K, Hodgson B, Burrows L, Shaw M, Wei C, Ullmann R, Ropers HH, Szepetowski P, Haan E, Mazarib A, Afawi Z, Neufeld MY, Andrews PI, Wallace G, Kivity S, Lev D, Lerman-Sagie T, Derry CP, Korczyn AD, Gecz J, Mulley JC, Berkovic SF.
    Brain; 2008 Apr 24; 131(Pt 4):918-27. PubMed ID: 18234694
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  • 20. Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15).
    Matricardi S, Darra F, Spalice A, Basti C, Fontana E, Dalla Bernardina B, Elia M, Giordano L, Accorsi P, Cusmai R, De Liso P, Romeo A, Ragona F, Granata T, Concolino D, Carotenuto M, Pavone P, Pruna D, Striano P, Savasta S, Verrotti A.
    Acta Neurol Scand; 2018 Jun 24; 137(6):575-581. PubMed ID: 29363096
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