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Journal Abstract Search


189 related items for PubMed ID: 23788720

  • 21. Motor cortex and thalamic atrophy in Unverricht-Lundborg disease: voxel-based morphometric study.
    Koskenkorva P, Khyuppenen J, Niskanen E, Könönen M, Bendel P, Mervaala E, Lehesjoki AE, Kälviäinen R, Vanninen R.
    Neurology; 2009 Aug 25; 73(8):606-11. PubMed ID: 19704079
    [Abstract] [Full Text] [Related]

  • 22. Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
    Canafoglia L, Gennaro E, Capovilla G, Gobbi G, Boni A, Beccaria F, Viri M, Michelucci R, Agazzi P, Assereto S, Coviello DA, Di Stefano M, Rossi Sebastiano D, Franceschetti S, Zara F.
    Epilepsia; 2012 Dec 25; 53(12):2120-7. PubMed ID: 23205931
    [Abstract] [Full Text] [Related]

  • 23. Unverricht-Lundborg progressive myoclonus epilepsy in Oman.
    Santoshkumar B, Turnbull J, Minassian BA.
    Pediatr Neurol; 2008 Apr 25; 38(4):252-5. PubMed ID: 18358403
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  • 24. Symptomatic white matter changes in mild traumatic brain injury resemble pathologic features of early Alzheimer dementia.
    Fakhran S, Yaeger K, Alhilali L.
    Radiology; 2013 Oct 25; 269(1):249-57. PubMed ID: 23781117
    [Abstract] [Full Text] [Related]

  • 25. Whole brain white matter changes revealed by multiple diffusion metrics in multiple sclerosis: a TBSS study.
    Liu Y, Duan Y, He Y, Yu C, Wang J, Huang J, Ye J, Parizel PM, Li K, Shu N.
    Eur J Radiol; 2012 Oct 25; 81(10):2826-32. PubMed ID: 22172535
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  • 26. Clinically isolated syndrome suggestive of multiple sclerosis: voxelwise regional investigation of white and gray matter.
    Raz E, Cercignani M, Sbardella E, Totaro P, Pozzilli C, Bozzali M, Pantano P.
    Radiology; 2010 Jan 25; 254(1):227-34. PubMed ID: 20019140
    [Abstract] [Full Text] [Related]

  • 27. Can we differentiate true white matter fibers from pseudofibers inside a brain abscess cavity using geometrical diffusion tensor imaging metrics?
    Kumar M, Gupta RK, Nath K, Rathore RK, Bayu G, Trivedi R, Husain M, Prasad KN, Tripathi RP, Narayana PA.
    NMR Biomed; 2008 Jul 25; 21(6):581-8. PubMed ID: 18050359
    [Abstract] [Full Text] [Related]

  • 28. A pathogenetic hypothesis of Unverricht-Lundborg disease onset and progression.
    Franceschetti S, Sancini G, Buzzi A, Zucchini S, Paradiso B, Magnaghi G, Frassoni C, Chikhladze M, Avanzini G, Simonato M.
    Neurobiol Dis; 2007 Mar 25; 25(3):675-85. PubMed ID: 17188503
    [Abstract] [Full Text] [Related]

  • 29. Assessment of white matter microstructural integrity in children with syndromic craniosynostosis: a diffusion-tensor imaging study.
    Florisson JM, Dudink J, Koning IV, Hop WC, van Veelen ML, Mathijssen IM, Lequin MH.
    Radiology; 2011 Nov 25; 261(2):534-41. PubMed ID: 21852568
    [Abstract] [Full Text] [Related]

  • 30. Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations.
    Alakurtti K, Weber E, Rinne R, Theil G, de Haan GJ, Lindhout D, Salmikangas P, Saukko P, Lahtinen U, Lehesjoki AE.
    Eur J Hum Genet; 2005 Feb 25; 13(2):208-15. PubMed ID: 15483648
    [Abstract] [Full Text] [Related]

  • 31. Gray- and white-matter changes 1 year after first clinical episode of multiple sclerosis: MR imaging.
    Raz E, Cercignani M, Sbardella E, Totaro P, Pozzilli C, Bozzali M, Pantano P.
    Radiology; 2010 Nov 25; 257(2):448-54. PubMed ID: 20858849
    [Abstract] [Full Text] [Related]

  • 32. Neuropathological changes in a mouse model of progressive myoclonus epilepsy: cystatin B deficiency and Unverricht-Lundborg disease.
    Shannon P, Pennacchio LA, Houseweart MK, Minassian BA, Myers RM.
    J Neuropathol Exp Neurol; 2002 Dec 25; 61(12):1085-91. PubMed ID: 12484571
    [Abstract] [Full Text] [Related]

  • 33. [From gene to disease; progressive myoclonus epilepsy of Unverricht-Lundborg and mutations in the cystatin B gene].
    de Haan GJ, Halley DJ, Deelen WH, Lindhout D.
    Ned Tijdschr Geneeskd; 2002 May 04; 146(18):846-8. PubMed ID: 12038222
    [Abstract] [Full Text] [Related]

  • 34. Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb-/- Microglia.
    Körber I, Katayama S, Einarsdottir E, Krjutškov K, Hakala P, Kere J, Lehesjoki AE, Joensuu T.
    PLoS One; 2016 May 04; 11(6):e0158195. PubMed ID: 27355630
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  • 35. Unverricht-Lundborg disease.
    Crespel A, Ferlazzo E, Franceschetti S, Genton P, Gouider R, Kälviäinen R, Korja M, Lehtinen MK, Mervaala E, Simonato M, Vaarmann A.
    Epileptic Disord; 2016 Sep 01; 18(S2):28-37. PubMed ID: 27582036
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  • 36. Protein aggregation as a possible cause for pathology in a subset of familial Unverricht-Lundborg disease.
    Ceru S, Rabzelj S, Kopitar-Jerala N, Turk V, Zerovnik E.
    Med Hypotheses; 2005 Sep 01; 64(5):955-9. PubMed ID: 15780491
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  • 37. Reduced cystatin B activity correlates with enhanced cathepsin activity in progressive myoclonus epilepsy.
    Rinne R, Saukko P, Järvinen M, Lehesjoki AE.
    Ann Med; 2002 Sep 01; 34(5):380-5. PubMed ID: 12452481
    [Abstract] [Full Text] [Related]

  • 38. Sensorimotor, visual, and auditory cortical atrophy in Unverricht-Lundborg disease mapped with cortical thickness analysis.
    Koskenkorva P, Niskanen E, Hyppönen J, Könönen M, Mervaala E, Soininen H, Kälviäinen R, Vanninen R.
    AJNR Am J Neuroradiol; 2012 May 01; 33(5):878-83. PubMed ID: 22268086
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  • 39. Intrinsic damage to the major white matter tracts in patients with different clinical phenotypes of multiple sclerosis: a voxelwise diffusion-tensor MR study.
    Preziosa P, Rocca MA, Mesaros S, Pagani E, Stosic-Opincal T, Kacar K, Absinta M, Caputo D, Drulovic J, Comi G, Filippi M.
    Radiology; 2011 Aug 01; 260(2):541-50. PubMed ID: 21673227
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  • 40. Altered white matter integrity of forebrain in treatment-resistant depression: a diffusion tensor imaging study with tract-based spatial statistics.
    Guo WB, Liu F, Chen JD, Xu XJ, Wu RR, Ma CQ, Gao K, Tan CL, Sun XL, Xiao CQ, Chen HF, Zhao JP.
    Prog Neuropsychopharmacol Biol Psychiatry; 2012 Aug 07; 38(2):201-6. PubMed ID: 22504778
    [Abstract] [Full Text] [Related]


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