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Journal Abstract Search

163 related items for PubMed ID: 25484361

  • 1.
    ; . PubMed ID:
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  • 2. Malformation of the human superior olive in autistic spectrum disorders.
    Kulesza RJ, Lukose R, Stevens LV.
    Brain Res; 2011 Jan 07; 1367():360-71. PubMed ID: 20946889
    [Abstract] [Full Text] [Related]

  • 3. Epigenetics of autism spectrum disorders.
    Schanen NC.
    Hum Mol Genet; 2006 Oct 15; 15 Spec No 2():R138-50. PubMed ID: 16987877
    [Abstract] [Full Text] [Related]

  • 4. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C.
    Biol Psychiatry; 2009 Aug 15; 66(4):349-59. PubMed ID: 19278672
    [Abstract] [Full Text] [Related]

  • 5. Longitudinal follow-up of autism spectrum features and sensory behaviors in Angelman syndrome by deletion class.
    Peters SU, Horowitz L, Barbieri-Welge R, Taylor JL, Hundley RJ.
    J Child Psychol Psychiatry; 2012 Feb 15; 53(2):152-9. PubMed ID: 21831244
    [Abstract] [Full Text] [Related]

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  • 7. Significant neuronal soma volume deficit in the limbic system in subjects with 15q11.2-q13 duplications.
    Wegiel J, Flory M, Schanen NC, Cook EH, Nowicki K, Kuchna I, Imaki H, Ma SY, Wegiel J, London E, Casanova MF, Wisniewski T, Brown WT.
    Acta Neuropathol Commun; 2015 Oct 13; 3():63. PubMed ID: 26463344
    [Abstract] [Full Text] [Related]

  • 8. Gastrointestinal problems in 15q duplication syndrome.
    Shaaya EA, Pollack SF, Boronat S, Davis-Cooper S, Zella GC, Thibert RL.
    Eur J Med Genet; 2015 Mar 13; 58(3):191-3. PubMed ID: 25573720
    [Abstract] [Full Text] [Related]

  • 9. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW.
    J Med Genet; 2010 Mar 13; 47(3):195-203. PubMed ID: 19755429
    [Abstract] [Full Text] [Related]

  • 10. Three dimensional reconstructions of the superior olivary complex from children with autism spectrum disorder.
    Mansour Y, Kulesza R.
    Hear Res; 2020 Aug 13; 393():107974. PubMed ID: 32540615
    [Abstract] [Full Text] [Related]

  • 11. Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders.
    Ozgen HM, van Daalen E, Bolton PF, Maloney VK, Huang S, Cresswell L, van den Boogaard MJ, Eleveld MJ, van 't Slot R, Hochstenbach R, Beemer FA, Barrow M, Barber JC, Poot M.
    Clin Genet; 2009 Oct 13; 76(4):348-56. PubMed ID: 19793310
    [Abstract] [Full Text] [Related]

  • 12. Two genetic variants of CD38 in subjects with autism spectrum disorder and controls.
    Munesue T, Yokoyama S, Nakamura K, Anitha A, Yamada K, Hayashi K, Asaka T, Liu HX, Jin D, Koizumi K, Islam MS, Huang JJ, Ma WJ, Kim UH, Kim SJ, Park K, Kim D, Kikuchi M, Ono Y, Nakatani H, Suda S, Miyachi T, Hirai H, Salmina A, Pichugina YA, Soumarokov AA, Takei N, Mori N, Tsujii M, Sugiyama T, Yagi K, Yamagishi M, Sasaki T, Yamasue H, Kato N, Hashimoto R, Taniike M, Hayashi Y, Hamada J, Suzuki S, Ooi A, Noda M, Kamiyama Y, Kido MA, Lopatina O, Hashii M, Amina S, Malavasi F, Huang EJ, Zhang J, Shimizu N, Yoshikawa T, Matsushima A, Minabe Y, Higashida H.
    Neurosci Res; 2010 Jun 13; 67(2):181-91. PubMed ID: 20435366
    [Abstract] [Full Text] [Related]

  • 13. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders.
    Bolton PF, Dennis NR, Browne CE, Thomas NS, Veltman MW, Thompson RJ, Jacobs P.
    Am J Med Genet; 2001 Dec 08; 105(8):675-85. PubMed ID: 11803514
    [Abstract] [Full Text] [Related]

  • 14. Hippocampal abnormalities in magnetic resonance imaging (MRI) of 15q duplication syndromes.
    Boronat S, Mehan WA, Shaaya EA, Thibert RL, Caruso P.
    J Child Neurol; 2015 Mar 08; 30(3):333-8. PubMed ID: 24985752
    [Abstract] [Full Text] [Related]

  • 15. Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism.
    Wegiel J, Schanen NC, Cook EH, Sigman M, Brown WT, Kuchna I, Nowicki K, Wegiel J, Imaki H, Ma SY, Marchi E, Wierzba-Bobrowicz T, Chauhan A, Chauhan V, Cohen IL, London E, Flory M, Lach B, Wisniewski T.
    J Neuropathol Exp Neurol; 2012 May 08; 71(5):382-97. PubMed ID: 22487857
    [Abstract] [Full Text] [Related]

  • 16. Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.
    Chung BH, Drmic I, Marshall CR, Grafodatskaya D, Carter M, Fernandez BA, Weksberg R, Roberts W, Scherer SW.
    Eur J Med Genet; 2011 May 08; 54(5):e516-20. PubMed ID: 21689796
    [Abstract] [Full Text] [Related]

  • 17. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
    Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL.
    Autism Res; 2009 Dec 08; 2(6):359-64. PubMed ID: 20029827
    [Abstract] [Full Text] [Related]

  • 18. Electro-clinical features in epileptic children with chromosome 15q duplication syndrome.
    Dangles MT, Malan V, Dumas G, Romana S, Raoul O, Coste-Zeitoun D, Soufflet C, Vignolo-Diard P, Bahi-Buisson N, Barnérias C, Chemaly N, Desguerre I, Gitiaux C, Hully M, Bourgeois M, Guimier A, Rio M, Munnich A, Nabbout R, Kaminska A, Eisermann M.
    Clin Neurophysiol; 2021 May 08; 132(5):1126-1137. PubMed ID: 33773177
    [Abstract] [Full Text] [Related]

  • 19. Critical roles of serotonin-oxytocin interaction during the neonatal period in social behavior in 15q dup mice with autistic traits.
    Nagano M, Takumi T, Suzuki H.
    Sci Rep; 2018 Sep 12; 8(1):13675. PubMed ID: 30209293
    [Abstract] [Full Text] [Related]

  • 20. Sexual dimorphic effect in the genetic association of monoamine oxidase A (MAOA) markers with autism spectrum disorder.
    Verma D, Chakraborti B, Karmakar A, Bandyopadhyay T, Singh AS, Sinha S, Chatterjee A, Ghosh S, Mohanakumar KP, Mukhopadhyay K, Rajamma U.
    Prog Neuropsychopharmacol Biol Psychiatry; 2014 Apr 03; 50():11-20. PubMed ID: 24291416
    [Abstract] [Full Text] [Related]

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