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Journal Abstract Search

193 related items for PubMed ID: 17596717

  • 41. Frontotemporal lobar degeneration: clinical and pathological relationships.
    Snowden J, Neary D, Mann D.
    Acta Neuropathol; 2007 Jul; 114(1):31-8. PubMed ID: 17569065
    [Abstract] [Full Text] [Related]

  • 42. Progranulin mutations in Dutch familial frontotemporal lobar degeneration.
    Bronner IF, Rizzu P, Seelaar H, van Mil SE, Anar B, Azmani A, Donker Kaat L, Rosso S, Heutink P, van Swieten JC.
    Eur J Hum Genet; 2007 Mar; 15(3):369-74. PubMed ID: 17228326
    [Abstract] [Full Text] [Related]

  • 43. Fine structural analysis of the neuronal inclusions of frontotemporal lobar degeneration with TDP-43 proteinopathy.
    Thorpe JR, Tang H, Atherton J, Cairns NJ.
    J Neural Transm (Vienna); 2008 Dec; 115(12):1661-71. PubMed ID: 18974920
    [Abstract] [Full Text] [Related]

  • 44. TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions.
    Neumann M, Kwong LK, Truax AC, Vanmassenhove B, Kretzschmar HA, Van Deerlin VM, Clark CM, Grossman M, Miller BL, Trojanowski JQ, Lee VM.
    J Neuropathol Exp Neurol; 2007 Mar; 66(3):177-83. PubMed ID: 17356379
    [Abstract] [Full Text] [Related]

  • 45. Clinicopathologic correlation in PGRN mutations.
    Davion S, Johnson N, Weintraub S, Mesulam MM, Engberg A, Mishra M, Baker M, Adamson J, Hutton M, Rademakers R, Bigio EH.
    Neurology; 2007 Sep 11; 69(11):1113-21. PubMed ID: 17522386
    [Abstract] [Full Text] [Related]

  • 46. Enhanced ATPase activities as a primary defect of mutant valosin-containing proteins that cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
    Manno A, Noguchi M, Fukushi J, Motohashi Y, Kakizuka A.
    Genes Cells; 2010 Aug 11; 15(8):911-22. PubMed ID: 20604808
    [Abstract] [Full Text] [Related]

  • 47. Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions.
    Josephs KA, Lin WL, Ahmed Z, Stroh DA, Graff-Radford NR, Dickson DW.
    Acta Neuropathol; 2008 Aug 11; 116(2):159-67. PubMed ID: 18553091
    [Abstract] [Full Text] [Related]

  • 48. Progranulin (PGRN) expression in ALS: an immunohistochemical study.
    Irwin D, Lippa CF, Rosso A.
    J Neurol Sci; 2009 Jan 15; 276(1-2):9-13. PubMed ID: 18848708
    [Abstract] [Full Text] [Related]

  • 49. Progranulin: normal function and role in neurodegeneration.
    Eriksen JL, Mackenzie IR.
    J Neurochem; 2008 Jan 15; 104(2):287-97. PubMed ID: 17953663
    [Abstract] [Full Text] [Related]

  • 50. Frontotemporal dementias: update on recent developments in molecular genetics and neuropathology.
    Liscić RM.
    Arh Hig Rada Toksikol; 2009 Mar 15; 60(1):117-22. PubMed ID: 19329383
    [Abstract] [Full Text] [Related]

  • 51. VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death.
    Gitcho MA, Strider J, Carter D, Taylor-Reinwald L, Forman MS, Goate AM, Cairns NJ.
    J Biol Chem; 2009 May 01; 284(18):12384-98. PubMed ID: 19237541
    [Abstract] [Full Text] [Related]

  • 52. Hippocampal sclerosis in tau-negative frontotemporal lobar degeneration.
    Josephs KA, Dickson DW.
    Neurobiol Aging; 2007 Nov 01; 28(11):1718-22. PubMed ID: 16930776
    [Abstract] [Full Text] [Related]

  • 53. TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD.
    Roeber S, Mackenzie IR, Kretzschmar HA, Neumann M.
    Acta Neuropathol; 2008 Aug 01; 116(2):147-57. PubMed ID: 18536926
    [Abstract] [Full Text] [Related]

  • 54. Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients.
    Kaivorinne AL, Krüger J, Udd B, Majamaa K, Remes AM.
    Eur J Neurol; 2010 Nov 01; 17(11):1393-5. PubMed ID: 20412296
    [Abstract] [Full Text] [Related]

  • 55. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
    Gass J, Cannon A, Mackenzie IR, Boeve B, Baker M, Adamson J, Crook R, Melquist S, Kuntz K, Petersen R, Josephs K, Pickering-Brown SM, Graff-Radford N, Uitti R, Dickson D, Wszolek Z, Gonzalez J, Beach TG, Bigio E, Johnson N, Weintraub S, Mesulam M, White CL, Woodruff B, Caselli R, Hsiung GY, Feldman H, Knopman D, Hutton M, Rademakers R.
    Hum Mol Genet; 2006 Oct 15; 15(20):2988-3001. PubMed ID: 16950801
    [Abstract] [Full Text] [Related]

  • 56. Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype.
    Mackenzie IR, Baborie A, Pickering-Brown S, Du Plessis D, Jaros E, Perry RH, Neary D, Snowden JS, Mann DM.
    Acta Neuropathol; 2006 Nov 15; 112(5):539-49. PubMed ID: 17021754
    [Abstract] [Full Text] [Related]

  • 57. Survival in two variants of tau-negative frontotemporal lobar degeneration: FTLD-U vs FTLD-MND.
    Josephs KA, Knopman DS, Whitwell JL, Boeve BF, Parisi JE, Petersen RC, Dickson DW.
    Neurology; 2005 Aug 23; 65(4):645-7. PubMed ID: 16116138
    [Abstract] [Full Text] [Related]

  • 58. Progranulin null mutations in both sporadic and familial frontotemporal dementia.
    Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerrière A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Antérion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A, French Research Network on FTD/FTD-MND.
    Hum Mutat; 2007 Sep 23; 28(9):846-55. PubMed ID: 17436289
    [Abstract] [Full Text] [Related]

  • 59. Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia.
    Snowden JS, Pickering-Brown SM, Mackenzie IR, Richardson AM, Varma A, Neary D, Mann DM.
    Brain; 2006 Nov 23; 129(Pt 11):3091-102. PubMed ID: 17003069
    [Abstract] [Full Text] [Related]

  • 60. Frontotemporal lobar degeneration with ubiquitin pathology: an autopsy case presenting with semantic dementia and upper motor neuron signs with a clinical course of 19 years.
    Yokota O, Tsuchiya K, Itoh Y, Ishizu H, Akiyama H, Ikeda M, Kuzuhara S, Otomo E.
    Acta Neuropathol; 2006 Dec 23; 112(6):739-49. PubMed ID: 17016698
    [Abstract] [Full Text] [Related]

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