These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

193 related items for PubMed ID: 17596717

  • 21. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease.
    Rovelet-Lecrux A, Deramecourt V, Legallic S, Maurage CA, Le Ber I, Brice A, Lambert JC, Frébourg T, Hannequin D, Pasquier F, Campion D.
    Neurobiol Dis; 2008 Jul; 31(1):41-5. PubMed ID: 18479928
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations.
    Forman MS, Mackenzie IR, Cairns NJ, Swanson E, Boyer PJ, Drachman DA, Jhaveri BS, Karlawish JH, Pestronk A, Smith TW, Tu PH, Watts GD, Markesbery WR, Smith CD, Kimonis VE.
    J Neuropathol Exp Neurol; 2006 Jun; 65(6):571-81. PubMed ID: 16783167
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Frontotemporal lobar degeneration and ubiquitin immunohistochemistry.
    Josephs KA, Holton JL, Rossor MN, Godbolt AK, Ozawa T, Strand K, Khan N, Al-Sarraj S, Revesz T.
    Neuropathol Appl Neurobiol; 2004 Aug; 30(4):369-73. PubMed ID: 15305982
    [Abstract] [Full Text] [Related]

  • 26. Mutant valosin-containing protein causes a novel type of frontotemporal dementia.
    Schröder R, Watts GD, Mehta SG, Evert BO, Broich P, Fliessbach K, Pauls K, Hans VH, Kimonis V, Thal DR.
    Ann Neurol; 2005 Mar; 57(3):457-61. PubMed ID: 15732117
    [Abstract] [Full Text] [Related]

  • 27. Recent advances in the genetics of amyotrophic lateral sclerosis and frontotemporal dementia: common pathways in neurodegenerative disease.
    Talbot K, Ansorge O.
    Hum Mol Genet; 2006 Oct 15; 15 Spec No 2():R182-7. PubMed ID: 16987882
    [Abstract] [Full Text] [Related]

  • 28. The heritability and genetics of frontotemporal lobar degeneration.
    Rohrer JD, Guerreiro R, Vandrovcova J, Uphill J, Reiman D, Beck J, Isaacs AM, Authier A, Ferrari R, Fox NC, Mackenzie IR, Warren JD, de Silva R, Holton J, Revesz T, Hardy J, Mead S, Rossor MN.
    Neurology; 2009 Nov 03; 73(18):1451-6. PubMed ID: 19884572
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.
    Mackenzie IR, Baker M, Pickering-Brown S, Hsiung GY, Lindholm C, Dwosh E, Gass J, Cannon A, Rademakers R, Hutton M, Feldman HH.
    Brain; 2006 Nov 03; 129(Pt 11):3081-90. PubMed ID: 17071926
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.
    Benussi L, Ghidoni R, Pegoiani E, Moretti DV, Zanetti O, Binetti G.
    Neurobiol Dis; 2009 Mar 03; 33(3):379-85. PubMed ID: 19101631
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. [Frontotemporal dementia (FTD) and genetic mutations including progranulin gene].
    Arai T, Hasegawa M, Nishihara M, Nonaka T, Kametani F, Yoshida M, Hashizume Y, Beach TG, Morita M, Nakano I, Oda T, Tsuchiya K, Akiyama H.
    Rinsho Shinkeigaku; 2008 Nov 03; 48(11):990-3. PubMed ID: 19198141
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.