BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

244 related articles for article (PubMed ID: 16967367)

  • 1. Aicardi syndrome: presentation at onset in Swedish children born in 1975-2002.
    Palmér L; Zetterlund B; Hård AL; Steneryd K; Kyllerman M
    Neuropediatrics; 2006 Jun; 37(3):154-8. PubMed ID: 16967367
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Aicardi syndrome: follow-up investigation of Swedish children born in 1975-2002.
    Palmér L; Zetterlund B; Hård AL; Steneryd K; Kyllerman M
    Neuropediatrics; 2007 Aug; 38(4):188-92. PubMed ID: 18058626
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children.
    Glasmacher MA; Sutton VR; Hopkins B; Eble T; Lewis RA; Park Parsons D; Van den Veyver IB
    J Child Neurol; 2007 Feb; 22(2):176-84. PubMed ID: 17621479
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases].
    Siegler Z; Neuwirth M; Hegyi M; Paraicz E; Pálmafy B; Tegzes A; Barsi P; Karcagi V; Claes L; De Jonghe P; Herczegfalvi A; Fogarasi A
    Ideggyogy Sz; 2008 Nov; 61(11-12):402-8. PubMed ID: 19070316
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical, cytogenetic, and pedigree findings in 18 cases of Aicardi syndrome.
    Donnenfeld AE; Packer RJ; Zackai EH; Chee CM; Sellinger B; Emanuel BS
    Am J Med Genet; 1989 Apr; 32(4):461-7. PubMed ID: 2773986
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Aicardi syndrome associated with anterior cephalocele in a female infant.
    Melbourne-Chambers R; Singh Minott I; Mowatt L; Johnson P; Thame M
    Dev Med Child Neurol; 2007 Jun; 49(6):464-6. PubMed ID: 17518934
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Aicardi syndrome.
    Rosser T
    Arch Neurol; 2003 Oct; 60(10):1471-3. PubMed ID: 14568821
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Treatment of epilepsy in severely disabled children with bilateral brain malformations.
    Saito Y; Sugai K; Nakagawa E; Sakuma H; Komaki H; Sasaki M; Maegaki Y; Ohno K; Sato N; Kaneko Y; Otsuki T
    J Neurol Sci; 2009 Feb; 277(1-2):37-49. PubMed ID: 19036389
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epilepsy in children with methylmalonic acidemia: electroclinical features and prognosis.
    Ma X; Zhang Y; Yang Y; Liu X; Yang Z; Bao X; Qin J; Wu X
    Brain Dev; 2011 Oct; 33(9):790-5. PubMed ID: 21764232
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spectrum of corpus callosum agenesis.
    Sztriha L
    Pediatr Neurol; 2005 Feb; 32(2):94-101. PubMed ID: 15664768
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnostic inaccuracy in children referred with "first seizure": role for a first seizure clinic.
    Hamiwka LD; Singh N; Niosi J; Wirrell EC
    Epilepsia; 2007 Jun; 48(6):1062-6. PubMed ID: 17553117
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Long-term prognosis for symptomatic (secondarily) generalized epilepsies: a population-based study.
    Camfield P; Camfield C
    Epilepsia; 2007 Jun; 48(6):1128-32. PubMed ID: 17442010
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 131(Pt 4):918-27. PubMed ID: 18234694
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Assessment of EEG in children with partial epilepsy].
    Zajac A; Kubik A; Kaciński M
    Przegl Lek; 2006; 63(11):1181-90. PubMed ID: 17348413
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Focal cortical dysplasia type 1b as a cause of severe epilepsy with multiple independent spike foci.
    Buoni S; Zannolli R; Miracco C; Macucci F; Hayek J; Burroni L; di Pietro G; Sardo L; Mussa F; Giordano F; Genitori L
    Brain Dev; 2008 Jan; 30(1):53-8. PubMed ID: 17583458
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Aicardi syndrome in a genotypic male.
    Chappelow AV; Reid J; Parikh S; Traboulsi EI
    Ophthalmic Genet; 2008 Dec; 29(4):181-3. PubMed ID: 19005990
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Agenesis of the corpus callosum].
    Nielsen LH
    Ugeskr Laeger; 1995 Feb; 157(6):737-9. PubMed ID: 7701633
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Outcome after corpus callosotomy in children with injurious drop attacks and severe mental retardation.
    Rathore C; Abraham M; Rao RM; George A; Sankara Sarma P; Radhakrishnan K
    Brain Dev; 2007 Oct; 29(9):577-85. PubMed ID: 17507193
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Aicardi syndrome in a male patient.
    Anderson S; Menten B; Kogelenberg Mv; Robertson S; Waginger M; Mentzel HJ; Brandl U; Skirl G; Willems P
    Neuropediatrics; 2009 Feb; 40(1):39-42. PubMed ID: 19639527
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.