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

208 related items for PubMed ID: 29095329

  • 1. Novel GFAP Variant in Adult-onset Alexander Disease With Progressive Ataxia and Palatal Tremor.
    Gass JM, Cheema A, Jackson J, Blackburn PR, Van Gerpen J, Atwal PS.
    Neurologist; 2017 Nov; 22(6):247-248. PubMed ID: 29095329
    [Abstract] [Full Text] [Related]

  • 2. Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature.
    Pareyson D, Fancellu R, Mariotti C, Romano S, Salmaggi A, Carella F, Girotti F, Gattellaro G, Carriero MR, Farina L, Ceccherini I, Savoiardo M.
    Brain; 2008 Sep; 131(Pt 9):2321-31. PubMed ID: 18684770
    [Abstract] [Full Text] [Related]

  • 3. Familial adult-onset Alexander disease with a novel mutation (D78N) in the glial fibrillary acidic protein gene with unusual bilateral basal ganglia involvement.
    Wada Y, Yanagihara C, Nishimura Y, Namekawa M.
    J Neurol Sci; 2013 Aug 15; 331(1-2):161-4. PubMed ID: 23743246
    [Abstract] [Full Text] [Related]

  • 4. Adult-onset Alexander disease with progressive ataxia and palatal tremor.
    Howard KL, Hall DA, Moon M, Agarwal P, Newman E, Brenner M.
    Mov Disord; 2008 Jan 15; 23(1):118-22. PubMed ID: 17960815
    [Abstract] [Full Text] [Related]

  • 5. Novel GFAP mutation in patient with adult-onset Alexander disease presenting with spastic ataxia.
    Kaneko H, Hirose M, Katada S, Takahashi T, Naruse S, Tsuchiya M, Yoshida T, Nakagawa M, Onodera O, Nishizawa M, Ikeuchi T.
    Mov Disord; 2009 Jul 15; 24(9):1393-5. PubMed ID: 19412928
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. An unusual presentation of late-onset Alexander's disease with slow orthostatic tremor and a novel GFAP variant.
    Stitt DW, Gavrilova R, Watson R, Hassan A.
    Neurocase; 2018 Jul 15; 24(5-6):266-268. PubMed ID: 30755139
    [Abstract] [Full Text] [Related]

  • 8. Dominantly-inherited adult-onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene.
    Thyagarajan D, Chataway T, Li R, Gai WP, Brenner M.
    Mov Disord; 2004 Oct 15; 19(10):1244-8. PubMed ID: 15390001
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients.
    Yoshida T, Sasayama H, Mizuta I, Okamoto Y, Yoshida M, Riku Y, Hayashi Y, Yonezu T, Takata Y, Ohnari K, Okuda S, Aiba I, Nakagawa M.
    Acta Neurol Scand; 2011 Aug 15; 124(2):104-8. PubMed ID: 20849398
    [Abstract] [Full Text] [Related]

  • 13. Clinical and genetic study in Chinese patients with Alexander disease.
    Ye Wu, Qiang Gu, Jingmin Wang, Yanling Yang, Xiru Wu, Yuwu Jiang.
    J Child Neurol; 2008 Feb 15; 23(2):173-7. PubMed ID: 18079314
    [Abstract] [Full Text] [Related]

  • 14. 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]

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

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Adult-onset Alexander disease : report on a family.
    Balbi P, Seri M, Ceccherini I, Uggetti C, Casale R, Fundarò C, Caroli F, Santoro L.
    J Neurol; 2008 Jan 15; 255(1):24-30. PubMed ID: 18004641
    [Abstract] [Full Text] [Related]

  • 19. Alexander disease with periventricular calcification: a novel mutation of the GFAP gene.
    Jefferson RJ, Absoud M, Jain R, Livingston JH, VAN DER Knaap MS, Jayawant S.
    Dev Med Child Neurol; 2010 Dec 15; 52(12):1160-3. PubMed ID: 20964669
    [Abstract] [Full Text] [Related]

  • 20. Alexander disease - astrogliopathy considered as leukodystrophy - experience of an institution.
    Mierzewska H, Mierzewska-Schmidt M, Salomons GS, Dudzińska M, Szczepanik E.
    Dev Period Med; 2016 Dec 15; 20(2):110-7. PubMed ID: 27442695
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.