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Journal Abstract Search

134 related items for PubMed ID: 22425009

  • 1. Multiple causes of apnea in 1p36 deletion syndrome include seizures.
    Kanabar G, Boyd S, Schugal A, Bhate S.
    Seizure; 2012 Jun; 21(5):402-6. PubMed ID: 22425009
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  • 2. Seizures and EEG pattern in the 22q13.3 deletion syndrome: clinical report of six Italian cases.
    Figura MG, Coppola A, Bottitta M, Calabrese G, Grillo L, Luciano D, Del Gaudio L, Torniero C, Striano S, Elia M.
    Seizure; 2014 Oct; 23(9):774-9. PubMed ID: 25027555
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  • 4. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
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  • 6. Seizure semiology and electroencephalography in young children with lesional temporal lobe epilepsy.
    Lv RJ, Sun ZR, Cui T, Shao XQ.
    Seizure; 2014 Feb; 23(2):155-7. PubMed ID: 24287079
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  • 8. Clinical and ictal characteristics of infantile seizures: EEG correlation via long-term video EEG monitoring.
    Yu HJ, Lee CG, Nam SH, Lee J, Lee M.
    Brain Dev; 2013 Sep; 35(8):771-7. PubMed ID: 23522623
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  • 9. Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome.
    Kurosawa K, Kawame H, Okamoto N, Ochiai Y, Akatsuka A, Kobayashi M, Shimohira M, Mizuno S, Wada K, Fukushima Y, Kawawaki H, Yamamoto T, Masuno M, Imaizumi K, Kuroki Y.
    Brain Dev; 2005 Aug; 27(5):378-82. PubMed ID: 16023556
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  • 10. Localization of pediatric seizure semiology.
    Vendrame M, Zarowski M, Alexopoulos AV, Wyllie E, Kothare SV, Loddenkemper T.
    Clin Neurophysiol; 2011 Oct; 122(10):1924-8. PubMed ID: 21474374
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  • 11. Proven startle-provoked epileptic seizures in childhood: semiologic and electrophysiologic variability.
    Tibussek D, Wohlrab G, Boltshauser E, Schmitt B.
    Epilepsia; 2006 Jun; 47(6):1050-8. PubMed ID: 16822252
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  • 12. Seizures and EEG patterns in Pallister-Killian syndrome: 13 new Italian patients.
    Giordano L, Viri M, Borgatti R, Lodi M, Accorsi P, Faravelli F, Ferretti MC, Grasso R, Memo L, Prola S, Pruna D, Santucci M, Savasta S, Verrotti A, Romeo A.
    Eur J Paediatr Neurol; 2012 Nov; 16(6):636-41. PubMed ID: 22464827
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  • 13. Growth patterns of patients with 1p36 deletion syndrome.
    Sangu N, Shimojima K, Shimada S, Ando T, Yamamoto T.
    Congenit Anom (Kyoto); 2014 May; 54(2):82-6. PubMed ID: 24750553
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  • 14. Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopia.
    Descartes M, Mikhail FM, Franklin JC, McGrath TM, Bebin M.
    Pediatr Neurol; 2011 Oct; 45(4):274-8. PubMed ID: 21907895
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  • 16. Anoxic-epileptic seizures: home video recordings of epileptic seizures induced by syncopes.
    Stephenson J, Breningstall G, Steer C, Kirkpatrick M, Horrocks I, Nechay A, Zuberi S.
    Epileptic Disord; 2004 Mar; 6(1):15-9. PubMed ID: 15075063
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  • 17. Neonatal apneic seizure of occipital lobe origin: continuous video-EEG recording.
    Castro Conde JR, González-Hernández T, González Barrios D, González Campo C.
    Pediatrics; 2012 Jun; 129(6):e1616-20. PubMed ID: 22641764
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  • 18. Clinical and EEG features of seizures in adults with down syndrome.
    Lefter S, Costello DJ, McNamara B, Sweeney B.
    J Clin Neurophysiol; 2011 Oct; 28(5):469-73. PubMed ID: 21946360
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  • 19. Lamotrigine adjunctive therapy among children and adolescents with primary generalized tonic-clonic seizures.
    Trevathan E, Kerls SP, Hammer AE, Vuong A, Messenheimer JA.
    Pediatrics; 2006 Aug; 118(2):e371-8. PubMed ID: 16847080
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  • 20. Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications.
    Shimada S, Shimojima K, Okamoto N, Sangu N, Hirasawa K, Matsuo M, Ikeuchi M, Shimakawa S, Shimizu K, Mizuno S, Kubota M, Adachi M, Saito Y, Tomiwa K, Haginoya K, Numabe H, Kako Y, Hayashi A, Sakamoto H, Hiraki Y, Minami K, Takemoto K, Watanabe K, Miura K, Chiyonobu T, Kumada T, Imai K, Maegaki Y, Nagata S, Kosaki K, Izumi T, Nagai T, Yamamoto T.
    Brain Dev; 2015 May; 37(5):515-26. PubMed ID: 25172301
    [Abstract] [Full Text] [Related]

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