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Journal Abstract Search

189 related items for PubMed ID: 23788720

  • 61. Major white matter fiber changes in medically intractable neocortical epilepsy in children: a diffusion tensor imaging study.
    Kim H, Harrison A, Kankirawatana P, Rozzelle C, Blount J, Torgerson C, Knowlton R.
    Epilepsy Res; 2013 Feb; 103(2-3):211-20. PubMed ID: 22917916
    [Abstract] [Full Text] [Related]

  • 62. Abnormal motor cortical adaptation to external stimulus in Unverricht-Lundborg disease (progressive myoclonus type 1, EPM1).
    Julkunen P, Löfberg O, Kallioniemi E, Hyppönen J, Kälviäinen R, Mervaala E.
    J Neurophysiol; 2018 Aug 01; 120(2):617-623. PubMed ID: 29742025
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  • 63. White Matter tract involvement in brain tumors: a diffusion tensor imaging analysis.
    Yen PS, Teo BT, Chiu CH, Chen SC, Chiu TL, Su CF.
    Surg Neurol; 2009 Nov 01; 72(5):464-9; discussion 469. PubMed ID: 19608227
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  • 64. Microstructural and volumetric abnormalities of the putamen in juvenile myoclonic epilepsy.
    Keller SS, Ahrens T, Mohammadi S, Möddel G, Kugel H, Ringelstein EB, Deppe M.
    Epilepsia; 2011 Sep 01; 52(9):1715-24. PubMed ID: 21635242
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  • 65. Axonal loss of white matter in migraine without aura: a tract-based spatial statistics study.
    Yu D, Yuan K, Qin W, Zhao L, Dong M, Liu P, Yang X, Liu J, Sun J, Zhou G, von Deneen KM, Tian J.
    Cephalalgia; 2013 Jan 01; 33(1):34-42. PubMed ID: 23150889
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  • 66. DNA deamination enables direct PCR amplification of the cystatin B (CSTB) gene-associated dodecamer repeat expansion in myoclonus epilepsy type Unverricht-Lundborg.
    Weinhaeusel A, Morris MA, Antonarakis SE, Haas OA.
    Hum Mutat; 2003 Nov 01; 22(5):404-8. PubMed ID: 14517952
    [Abstract] [Full Text] [Related]

  • 67. Microstructural white matter abnormality and frontal cognitive dysfunctions in juvenile myoclonic epilepsy.
    Kim JH, Suh SI, Park SY, Seo WK, Koh I, Koh SB, Seol HY.
    Epilepsia; 2012 Aug 01; 53(8):1371-8. PubMed ID: 22708960
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  • 68. Sex differences in white matter abnormalities after mild traumatic brain injury: localization and correlation with outcome.
    Fakhran S, Yaeger K, Collins M, Alhilali L.
    Radiology; 2014 Sep 01; 272(3):815-23. PubMed ID: 24802388
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  • 69. Unverricht-Lundborg disease: homozygosity for a new splicing mutation in the cystatin B gene.
    Pinto E, Freitas J, Duarte AJ, Ribeiro I, Ribeiro D, Lima JL, Chaves J, Amaral O.
    Epilepsy Res; 2012 Mar 01; 99(1-2):187-90. PubMed ID: 22154554
    [Abstract] [Full Text] [Related]

  • 70. Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy.
    Lalioti MD, Scott HS, Buresi C, Rossier C, Bottani A, Morris MA, Malafosse A, Antonarakis SE.
    Nature; 1997 Apr 24; 386(6627):847-51. PubMed ID: 9126745
    [Abstract] [Full Text] [Related]

  • 71. High-resolution diffusion tensor imaging of fixed brain in a mouse model of Pelizaeus-Merzbacher disease: comparison with quantitative measures of white matter pathology.
    Ruest T, Holmes WM, Barrie JA, Griffiths IR, Anderson TJ, Dewar D, Edgar JM.
    NMR Biomed; 2011 Dec 24; 24(10):1369-79. PubMed ID: 22223367
    [Abstract] [Full Text] [Related]

  • 72. The Roles of Cystatin B in the Brain and Pathophysiological Mechanisms of Progressive Myoclonic Epilepsy Type 1.
    Singh S, Hämäläinen RH.
    Cells; 2024 Jan 16; 13(2):. PubMed ID: 38247861
    [Abstract] [Full Text] [Related]

  • 73. A new clinical and molecular form of Unverricht-Lundborg disease localized by homozygosity mapping.
    Berkovic SF, Mazarib A, Walid S, Neufeld MY, Manelis J, Nevo Y, Korczyn AD, Yin J, Xiong L, Pandolfo M, Mulley JC, Wallace RH.
    Brain; 2005 Mar 16; 128(Pt 3):652-8. PubMed ID: 15634728
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  • 74. Similar white matter aberrations in children with autism and their unaffected siblings: a diffusion tensor imaging study using tract-based spatial statistics.
    Barnea-Goraly N, Lotspeich LJ, Reiss AL.
    Arch Gen Psychiatry; 2010 Oct 16; 67(10):1052-60. PubMed ID: 20921121
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  • 75. Negative myoclonus causes locomotory disability in progressive myoclonus epilepsy type EPM1- Unverricht-Lundborg disease.
    Vogt H, Baisch T, Mueller-Pfeiffer C, Mothersill IW.
    Epileptic Disord; 2023 Jun 16; 25(3):297-308. PubMed ID: 37536959
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  • 76. Atypical development of white matter microstructure in adolescents with autism spectrum disorders.
    Cheng Y, Chou KH, Chen IY, Fan YT, Decety J, Lin CP.
    Neuroimage; 2010 Apr 15; 50(3):873-82. PubMed ID: 20074650
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  • 77. Diffusion changes in patients with systemic lupus erythematosus.
    Zhang L, Harrison M, Heier LA, Zimmerman RD, Ravdin L, Lockshin M, Uluğ AM.
    Magn Reson Imaging; 2007 Apr 15; 25(3):399-405. PubMed ID: 17371731
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  • 78. White-matter microstructural changes in functional dyspepsia: a diffusion tensor imaging study.
    Zhou G, Qin W, Zeng F, Liu P, Yang X, von Deneen KM, Gong Q, Liang F, Tian J.
    Am J Gastroenterol; 2013 Feb 15; 108(2):260-9. PubMed ID: 23229422
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  • 79. Nerve fiber impairment of anterior thalamocortical circuitry in juvenile myoclonic epilepsy.
    Deppe M, Kellinghaus C, Duning T, Möddel G, Mohammadi S, Deppe K, Schiffbauer H, Kugel H, Keller SS, Ringelstein EB, Knecht S.
    Neurology; 2008 Dec 09; 71(24):1981-5. PubMed ID: 19064879
    [Abstract] [Full Text] [Related]

  • 80. Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice.
    Pennacchio LA, Bouley DM, Higgins KM, Scott MP, Noebels JL, Myers RM.
    Nat Genet; 1998 Nov 09; 20(3):251-8. PubMed ID: 9806543
    [Abstract] [Full Text] [Related]

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