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

262 related items for PubMed ID: 20849398

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene.
    Stumpf E, Masson H, Duquette A, Berthelet F, McNabb J, Lortie A, Lesage J, Montplaisir J, Brais B, Cossette P.
    Arch Neurol; 2003 Sep; 60(9):1307-12. PubMed ID: 12975300
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Acute onset of adult Alexander disease.
    Schmidt H, Kretzschmar B, Lingor P, Pauli S, Schramm P, Otto M, Ohlenbusch A, Brockmann K.
    J Neurol Sci; 2013 Aug 15; 331(1-2):152-4. PubMed ID: 23706596
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease.
    Li R, Johnson AB, Salomons G, Goldman JE, Naidu S, Quinlan R, Cree B, Ruyle SZ, Banwell B, D'Hooghe M, Siebert JR, Rolf CM, Cox H, Reddy A, Gutiérrez-Solana LG, Collins A, Weller RO, Messing A, van der Knaap MS, Brenner M.
    Ann Neurol; 2005 Mar 15; 57(3):310-26. PubMed ID: 15732097
    [Abstract] [Full Text] [Related]

  • 9. Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease.
    Namekawa M, Takiyama Y, Aoki Y, Takayashiki N, Sakoe K, Shimazaki H, Taguchi T, Tanaka Y, Nishizawa M, Saito K, Matsubara Y, Nakano I.
    Ann Neurol; 2002 Dec 15; 52(6):779-85. PubMed ID: 12447932
    [Abstract] [Full Text] [Related]

  • 10. An infantile-juvenile form of Alexander disease caused by a R79H mutation in GFAP.
    Asahina N, Okamoto T, Sudo A, Kanazawa N, Tsujino S, Saitoh S.
    Brain Dev; 2006 Mar 15; 28(2):131-3. PubMed ID: 16168593
    [Abstract] [Full Text] [Related]

  • 11. Novel deletion mutation in GFAP gene in an infantile form of Alexander disease.
    Murakami N, Tsuchiya T, Kanazawa N, Tsujino S, Nagai T.
    Pediatr Neurol; 2008 Jan 15; 38(1):50-2. PubMed ID: 18054694
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease.
    Hartmann H, Herchenbach J, Stephani U, Ledaal P, Donnerstag F, Lücke T, Das AM, Christen HJ, Hagedorn M, Meins M.
    Neuropediatrics; 2007 Jun 15; 38(3):143-7. PubMed ID: 17985264
    [Abstract] [Full Text] [Related]

  • 17. A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis.
    Sakakibara T, Takahashi Y, Fukuda K, Inoue T, Kurosawa T, Nishikubo T, Shima M, Taoka T, Aida N, Tsujino S, Kanazawa N, Yoshioka A.
    Brain Dev; 2007 Sep 15; 29(8):525-8. PubMed ID: 17383133
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. An autopsied case of adult-onset bulbospinalform Alexander disease with a novel S393R mutation in the GFAP gene.
    Iwasaki Y, Saito Y, Mori K, Ito M, Mimuro M, Aiba I, Saito K, Mizuta I, Yoshida T, Nakagawa M, Yoshida M.
    Clin Neuropathol; 2015 Sep 15; 34(4):207-14. PubMed ID: 25828773
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.