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241 related items for PubMed ID: 20553986

  • 1. Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.
    Gerkes EH, Hordijk R, Dijkhuizen T, Sival DA, Meiners LC, Sikkema-Raddatz B, van Ravenswaaij-Arts CM.
    Eur J Med Genet; 2010; 53(5):344-6. PubMed ID: 20553986
    [Abstract] [Full Text] [Related]

  • 2. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G, Verdú-Pérez A, de Castro-De Castro P.
    Rev Neurol; 2010; 48(4):188-90. PubMed ID: 19226486
    [Abstract] [Full Text] [Related]

  • 3. Bilateral polymicrogyria: always think in chromosome 22q11.2 deletion syndromes.
    Castro A, Rodrigues N, Pereira M, Gonçalves C.
    BMJ Case Rep; 2011 Nov 23; 2011():. PubMed ID: 22674744
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  • 5. Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients.
    Gropman AL, Barkovich AJ, Vezina LG, Conry JA, Dubovsky EC, Packer RJ.
    Neuropediatrics; 1997 Aug 23; 28(4):198-203. PubMed ID: 9309709
    [Abstract] [Full Text] [Related]

  • 6. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.
    Robin NH, Taylor CJ, McDonald-McGinn DM, Zackai EH, Bingham P, Collins KJ, Earl D, Gill D, Granata T, Guerrini R, Katz N, Kimonis V, Lin JP, Lynch DR, Mohammed SN, Massey RF, McDonald M, Rogers RC, Splitt M, Stevens CA, Tischkowitz MD, Stoodley N, Leventer RJ, Pilz DT, Dobyns WB.
    Am J Med Genet A; 2006 Nov 15; 140(22):2416-25. PubMed ID: 17036343
    [Abstract] [Full Text] [Related]

  • 7. A familial syndrome of unilateral polymicrogyria affecting the right hemisphere.
    Chang BS, Apse KA, Caraballo R, Cross JH, Mclellan A, Jacobson RD, Valente KD, Barkovich AJ, Walsh CA.
    Neurology; 2006 Jan 10; 66(1):133-5. PubMed ID: 16401865
    [Abstract] [Full Text] [Related]

  • 8. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B, Kiratli H, Kılıç E, Utine E, Boduroğlu K.
    Ophthalmic Genet; 2014 Dec 10; 35(4):248-51. PubMed ID: 23834556
    [Abstract] [Full Text] [Related]

  • 9. 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 10; 128(Pt 12):2811-21. PubMed ID: 16311271
    [Abstract] [Full Text] [Related]

  • 10. Polymicrogyria in chromosome 22q11 deletion syndrome.
    Ghariani S, Dahan K, Saint-Martin C, Kadhim H, Morsomme F, Moniotte S, Verellen-Dumoulin C, Sébire G.
    Eur J Paediatr Neurol; 2002 Dec 10; 6(1):73-7. PubMed ID: 11993959
    [Abstract] [Full Text] [Related]

  • 11. [Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].
    Pinquier C, Héron D, de Carvalho W, Lazar G, Mazet P, Cohen D.
    Encephale; 2001 Dec 10; 27(1):45-50. PubMed ID: 11294038
    [Abstract] [Full Text] [Related]

  • 12. Chromosome 22q11 deletion syndrome: the first three cases reported in Thailand.
    Ruangdaraganon N, Tocharoentanaphol C, Khowsathit P, Sombuntham T, Pongpanich B.
    J Med Assoc Thai; 1999 Nov 10; 82 Suppl 1():S179-85. PubMed ID: 10730540
    [Abstract] [Full Text] [Related]

  • 13. Polymicrogyria: a common and heterogeneous malformation of cortical development.
    Stutterd CA, Leventer RJ.
    Am J Med Genet C Semin Med Genet; 2014 Jun 10; 166C(2):227-39. PubMed ID: 24888723
    [Abstract] [Full Text] [Related]

  • 14. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
    Kitsiou-Tzeli S, Kolialexi A, Fryssira H, Galla-Voumvouraki A, Salavoura K, Kanariou M, Tsangaris GT, Kanavakis E, Mavrou A.
    In Vivo; 2004 Jun 10; 18(5):603-8. PubMed ID: 15523900
    [Abstract] [Full Text] [Related]

  • 15. 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 10; 121(2):404-10. PubMed ID: 18245432
    [Abstract] [Full Text] [Related]

  • 16. Bilateral perisylvian polymicrogyria with cerebellar dysplasia and ectopic neurohypophysis.
    Toldo I, Calderone M, Sartori S, Mardari R, Gatta M, Boniver C, Guerrini R, Battistella PA.
    J Child Neurol; 2011 Mar 10; 26(3):361-5. PubMed ID: 21273507
    [Abstract] [Full Text] [Related]

  • 17. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
    Muñoz S, Garay F, Flores I, Heusser F, Talesnik E, Aracena M, Mellado C, Méndez C, Arnaiz P, Repetto G.
    Rev Med Chil; 2001 May 10; 129(5):515-21. PubMed ID: 11464533
    [Abstract] [Full Text] [Related]

  • 18. Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome.
    Saito Y, Kubota M, Kurosawa K, Ichihashi I, Kaneko Y, Hattori A, Komaki H, Nakagawa E, Sugai K, Sasaki M.
    Brain Dev; 2011 May 10; 33(5):437-41. PubMed ID: 20708863
    [Abstract] [Full Text] [Related]

  • 19. Neuroradiographic findings in 22q11.2 deletion syndrome.
    Bohm LA, Zhou TC, Mingo TJ, Dugan SL, Patterson RJ, Sidman JD, Roby BB.
    Am J Med Genet A; 2017 Aug 10; 173(8):2158-2165. PubMed ID: 28577347
    [Abstract] [Full Text] [Related]

  • 20. Congenital bilateral perisylvian syndrome: familial occurrence, clinical and psycholinguistic aspects correlated with MRI.
    Brandão-Almeida IL, Hage SR, Oliveira EP, Guimarães CA, Teixeira KC, Abramides DV, Montenegro MA, Santos NF, Cendes F, Lopes-Cendes I, Guerreiro MM.
    Neuropediatrics; 2008 Jun 10; 39(3):139-45. PubMed ID: 18991192
    [Abstract] [Full Text] [Related]

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