These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

554 related items for PubMed ID: 16495142

  • 1. Inv dup (15): is the electroclinical phenotype helpful for this challenging clinical diagnosis?
    Valente KD, Freitas A, Fridman C, Varela M, Silva AE, Fett AC, Koiffmann CP.
    Clin Neurophysiol; 2006 Apr; 117(4):803-9. PubMed ID: 16495142
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. Electroclinical characteristics of seizures-comparing Prader--Willi syndrome with Angelman syndrome.
    Wang PJ, Hou JW, Sue WC, Lee WT.
    Brain Dev; 2005 Mar; 27(2):101-7. PubMed ID: 15668048
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 7. Mild generalized epilepsy and developmental disorder associated with large inv dup(15).
    Chifari R, Guerrini R, Pierluigi M, Cavani S, Sgrò V, Elia M, Canger R, Canevini MP.
    Epilepsia; 2002 Sep 24; 43(9):1096-100. PubMed ID: 12199736
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 11. Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15.
    Takeda Y, Baba A, Nakamura F, Ito M, Honma H, Koyama T.
    Seizure; 2000 Mar 24; 9(2):145-50. PubMed ID: 10845741
    [Abstract] [Full Text] [Related]

  • 12. Symptomatic epilepsies imitating idiopathic generalized epilepsies.
    Oguni H.
    Epilepsia; 2005 Mar 24; 46 Suppl 9():84-90. PubMed ID: 16302880
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 14. FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.
    Cockwell AE, Dávalos IP, Rivera HR, Crolla JA.
    Am J Med Genet; 2001 Nov 01; 103(4):289-94. PubMed ID: 11746008
    [Abstract] [Full Text] [Related]

  • 15. Epilepsy in Menkes disease: analysis of clinical stages.
    Bahi-Buisson N, Kaminska A, Nabbout R, Barnerias C, Desguerre I, De Lonlay P, Mayer M, Plouin P, Dulac O, Chiron C.
    Epilepsia; 2006 Feb 01; 47(2):380-6. PubMed ID: 16499764
    [Abstract] [Full Text] [Related]

  • 16. Benign myoclonic epilepsy in infants: electroclinical features and long-term follow-up of 34 patients.
    Auvin S, Pandit F, De Bellecize J, Badinand N, Isnard H, Motte J, Villeneuve N, Lamblin MD, Vallée L.
    Epilepsia; 2006 Feb 01; 47(2):387-93. PubMed ID: 16499765
    [Abstract] [Full Text] [Related]

  • 17. Spectrum of epilepsy and electroencephalogram patterns in Wolf-Hirschhorn syndrome: experience with 87 patients.
    Battaglia A, Filippi T, South ST, Carey JC.
    Dev Med Child Neurol; 2009 May 01; 51(5):373-80. PubMed ID: 19379291
    [Abstract] [Full Text] [Related]

  • 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 May 01; 54(4):e446-50. PubMed ID: 21621018
    [Abstract] [Full Text] [Related]

  • 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 01; 131(Pt 4):918-27. PubMed ID: 18234694
    [Abstract] [Full Text] [Related]

  • 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 01; 137(6):575-581. PubMed ID: 29363096
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 28.