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Journal Abstract Search

195 related items for PubMed ID: 18925666

  • 1. Neuroimaging aspects of Aicardi syndrome.
    Hopkins B, Sutton VR, Lewis RA, Van den Veyver I, Clark G.
    Am J Med Genet A; 2008 Nov 15; 146A(22):2871-8. PubMed ID: 18925666
    [Abstract] [Full Text] [Related]

  • 2. Cerebellar migration defects in aicardi syndrome: an extension of the neuropathological spectrum.
    Steffensen TS, Gilbert-Barness E, Lacson A, Margo CE.
    Fetal Pediatr Pathol; 2009 Nov 15; 28(1):24-38. PubMed ID: 19116813
    [Abstract] [Full Text] [Related]

  • 3. Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.
    Conti V, Carabalona A, Pallesi-Pocachard E, Parrini E, Leventer RJ, Buhler E, McGillivray G, Michel FJ, Striano P, Mei D, Watrin F, Lise S, Pagnamenta AT, Taylor JC, Kini U, Clayton-Smith J, Novara F, Zuffardi O, Dobyns WB, Scheffer IE, Robertson SP, Berkovic SF, Represa A, Keays DA, Cardoso C, Guerrini R.
    Brain; 2013 Nov 15; 136(Pt 11):3378-94. PubMed ID: 24056535
    [Abstract] [Full Text] [Related]

  • 4. Bilateral posterior periventricular nodular heterotopia: a recognizable cortical malformation with a spectrum of associated brain abnormalities.
    Mandelstam SA, Leventer RJ, Sandow A, McGillivray G, van Kogelenberg M, Guerrini R, Robertson S, Berkovic SF, Jackson GD, Scheffer IE.
    AJNR Am J Neuroradiol; 2013 Feb 15; 34(2):432-8. PubMed ID: 23348762
    [Abstract] [Full Text] [Related]

  • 5. Aicardi syndrome.
    Singh P, Goraya JS, Saggar K, Ahluwalia A.
    Singapore Med J; 2012 Jul 15; 53(7):e153-5. PubMed ID: 22815034
    [Abstract] [Full Text] [Related]

  • 6. Periventricular nodular heterotopia with overlying polymicrogyria.
    Wieck G, Leventer RJ, Squier WM, Jansen A, Andermann E, Dubeau F, Ramazzotti A, Guerrini R, Dobyns WB.
    Brain; 2005 Dec 15; 128(Pt 12):2811-21. PubMed ID: 16311271
    [Abstract] [Full Text] [Related]

  • 7. Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome.
    Masnada S, Pichiecchio A, Formica M, Arrigoni F, Borrelli P, Accorsi P, Bonanni P, Borgatti R, Bernardina BD, Danieli A, Darra F, Deconinck N, De Giorgis V, Dulac O, Gataullina S, Giordano L, Guerrini R, La Briola F, Mastrangelo M, Montomoli M, Mortilla M, Osanni E, Parisi P, Perucca E, Pinelli L, Romaniello R, Severino M, Vigevano F, Vignoli A, Bahi-Buisson N, Cavallin M, Accogli A, Burgeois M, Capra V, Chaves-Vischer V, Chiapparini L, Colafati G, D'Arrigo S, Desguerre I, Doco-Fenzy M, d'Orsi G, Epitashvili N, Fazzi E, Ferretti A, Fiorini E, Fradin M, Fusco C, Granata T, Johannesen KM, Lebon S, Loget P, Moller RS, Montanaro D, Orcesi S, Quelin C, Rebessi E, Romeo A, Solazzi R, Spagnoli C, Uebler C, Zara F, Arzimanoglou A, Veggiotti P, Aicardi Syndrome International Study Group.
    Neurology; 2021 Mar 02; 96(9):e1319-e1333. PubMed ID: 33277420
    [Abstract] [Full Text] [Related]

  • 8. Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis.
    Pisano T, Barkovich AJ, Leventer RJ, Squier W, Scheffer IE, Parrini E, Blaser S, Marini C, Robertson S, Tortorella G, Rosenow F, Thomas P, McGillivray G, Andermann E, Andermann F, Berkovic SF, Dobyns WB, Guerrini R.
    Neurology; 2012 Sep 18; 79(12):1244-51. PubMed ID: 22914838
    [Abstract] [Full Text] [Related]

  • 9. Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.
    Parrini E, Ramazzotti A, Dobyns WB, Mei D, Moro F, Veggiotti P, Marini C, Brilstra EH, Dalla Bernardina B, Goodwin L, Bodell A, Jones MC, Nangeroni M, Palmeri S, Said E, Sander JW, Striano P, Takahashi Y, Van Maldergem L, Leonardi G, Wright M, Walsh CA, Guerrini R.
    Brain; 2006 Jul 18; 129(Pt 7):1892-906. PubMed ID: 16684786
    [Abstract] [Full Text] [Related]

  • 10. Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36.
    Saito S, Kawamura R, Kosho T, Shimizu T, Aoyama K, Koike K, Wada T, Matsumoto N, Kato M, Wakui K, Fukushima Y.
    Am J Med Genet A; 2008 Nov 15; 146A(22):2891-7. PubMed ID: 18925681
    [Abstract] [Full Text] [Related]

  • 11. Aicardi syndrome choroid plexus cysts.
    Herman TE, Lee BC, Siegel MJ.
    J Perinatol; 2007 May 15; 27(5):323-4. PubMed ID: 17453044
    [No Abstract] [Full Text] [Related]

  • 12. Iris cyst in a child with Aicardi syndrome: a novel association.
    Chappaz A, Barthelmes D, Buser L, Funk J, Gerth-Kahlert C.
    J AAPOS; 2016 Oct 15; 20(5):451-452. PubMed ID: 27320016
    [Abstract] [Full Text] [Related]

  • 13. Clinical and neuroimaging findings in children with gray matter heterotopias: A single institution experience of 36 patients.
    Hung PC, Wang HS, Chou ML, Lin KL, Hsieh MY, Wong AM.
    Eur J Paediatr Neurol; 2016 Sep 15; 20(5):732-7. PubMed ID: 27262615
    [Abstract] [Full Text] [Related]

  • 14. [Clinical outcome of distinct Aicardi syndrome phenotypes].
    Galdós M, Martínez R, Prats JM.
    Arch Soc Esp Oftalmol; 2008 Jan 15; 83(1):29-36. PubMed ID: 18188792
    [Abstract] [Full Text] [Related]

  • 15. Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.
    Conway RL, Pressman BD, Dobyns WB, Danielpour M, Lee J, Sanchez-Lara PA, Butler MG, Zackai E, Campbell L, Saitta SC, Clericuzio CL, Milunsky JM, Hoyme HE, Shieh J, Moeschler JB, Crandall B, Lauzon JL, Viskochil DH, Harding B, Graham JM.
    Am J Med Genet A; 2007 Dec 15; 143A(24):2981-3008. PubMed ID: 18000912
    [Abstract] [Full Text] [Related]

  • 16. Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development.
    Uccella S, Accogli A, Tortora D, Mancardi MM, Nobili L, Berloco B, Morana G, Striano P, Capra V, Srour M, Saint-Martine C, Rossi A, Severino M.
    J Neurol; 2019 May 15; 266(5):1167-1181. PubMed ID: 30796522
    [Abstract] [Full Text] [Related]

  • 17. Asymmetric polymicrogyria and periventricular nodular heterotopia due to mutation in ARX.
    Oegema R, Maat-Kievit A, Lequin MH, Schot R, Nanninga-van den Neste VM, Doornbos ME, de Wit MC, Halley DJ, Mancini GM.
    Am J Med Genet A; 2012 Jun 15; 158A(6):1472-6. PubMed ID: 22585566
    [Abstract] [Full Text] [Related]

  • 18. The Clinical Picture of a Bilateral Perisylvian Syndrome as the Initial Symptom of Mega-Corpus-Callosum Syndrome due to a MAST1-Gene Mutation.
    Hecher L, Johannsen J, Bierhals T, Buhk JH, Hempel M, Denecke J.
    Neuropediatrics; 2020 Dec 15; 51(6):435-439. PubMed ID: 32818970
    [Abstract] [Full Text] [Related]

  • 19. Posterior fossa malformation associated with cerebral anomalies: genetic and imaging features.
    Bertholdo D, de Carvalho Neto A, Castillo M.
    Top Magn Reson Imaging; 2011 Dec 15; 22(6):295-302. PubMed ID: 24132068
    [Abstract] [Full Text] [Related]

  • 20. Agenesis of the Corpus Callosum and Aicardi Syndrome: A Neuroimaging and Clinical Comparison.
    Govil-Dalela T, Kumar A, Agarwal R, Chugani HT.
    Pediatr Neurol; 2017 Mar 15; 68():44-48.e2. PubMed ID: 28214165
    [Abstract] [Full Text] [Related]

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