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

168 related items for PubMed ID: 18581469

  • 1. Alexander disease causing hereditary late-onset ataxia with only minimal white matter changes: A report of two sibs.
    Delnooz CC, Schelhaas JH, van de Warrenburg BP, de Graaf RJ, Salomons GS.
    Mov Disord; 2008 Aug 15; 23(11):1613-5. PubMed ID: 18581469
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Serial MRI changes in a patient with infantile Alexander disease and prolonged survival.
    Shiihara T, Yoneda T, Mizuta I, Yoshida T, Nakagawa M, Shimizu N.
    Brain Dev; 2011 Aug 15; 33(7):604-7. PubMed ID: 21041050
    [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. Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.
    van der Knaap MS, Ramesh V, Schiffmann R, Blaser S, Kyllerman M, Gholkar A, Ellison DW, van der Voorn JP, van Dooren SJ, Jakobs C, Barkhof F, Salomons GS.
    Neurology; 2006 Feb 28; 66(4):494-8. PubMed ID: 16505300
    [Abstract] [Full Text] [Related]

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

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

  • 8. 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 28; 131(Pt 9):2321-31. PubMed ID: 18684770
    [Abstract] [Full Text] [Related]

  • 9. Alexander disease with occipital predominance and a novel c.799G>C mutation in the GFAP gene.
    Hinttala R, Karttunen V, Karttunen A, Herva R, Uusimaa J, Remes AM.
    Acta Neuropathol; 2007 Nov 28; 114(5):543-5. PubMed ID: 17805552
    [No Abstract] [Full Text] [Related]

  • 10. A practical approach to late-onset cerebellar ataxia: putting the disorder with lack of order into order.
    van Gaalen J, van de Warrenburg BP.
    Pract Neurol; 2012 Feb 28; 12(1):14-24. PubMed ID: 22258168
    [Abstract] [Full Text] [Related]

  • 11. The ocular motor features of adult-onset alexander disease: a case and review of the literature.
    Pfeffer G, Abegg M, Vertinsky AT, Ceccherini I, Caroli F, Barton JJ.
    J Neuroophthalmol; 2011 Jun 28; 31(2):155-9. PubMed ID: 21403579
    [Abstract] [Full Text] [Related]

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

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

  • 14. Patterns of fractional anisotropy changes in white matter of cerebellar peduncles distinguish spinocerebellar ataxia-1 from multiple system atrophy and other ataxia syndromes.
    Prakash N, Hageman N, Hua X, Toga AW, Perlman SL, Salamon N.
    Neuroimage; 2009 Aug 28; 47 Suppl 2():T72-81. PubMed ID: 19446636
    [Abstract] [Full Text] [Related]

  • 15. Tumor-like enlargement of the optic chiasm in an infant with Alexander disease.
    Mignot C, Desguerre I, Burglen L, Hertz-Pannier L, Renaldo F, Gadisseux JF, Gallet S, Pham-Dinh D, Boespflug-Tanguy O, Rodriguez D.
    Brain Dev; 2009 Mar 28; 31(3):244-7. PubMed ID: 18584981
    [Abstract] [Full Text] [Related]

  • 16. 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 28; 29(8):525-8. PubMed ID: 17383133
    [Abstract] [Full Text] [Related]

  • 17. 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 28; 28(2):131-3. PubMed ID: 16168593
    [Abstract] [Full Text] [Related]

  • 18. [An autopsied case of dentato-rubro-pallido-luysian atrophy with atypical pathological lesions].
    Konagaya M, Sakai M, Kato T, Kuru S, Matsuoka Y, Sobue G, Hashizume Y, Yoshida M.
    No To Shinkei; 2002 Jun 28; 54(6):513-20. PubMed ID: 12166103
    [Abstract] [Full Text] [Related]

  • 19. Alexander disease: combined gene analysis and MRI clarify pathogenesis and extend phenotype.
    Moser HW.
    Ann Neurol; 2005 Mar 28; 57(3):307-8. PubMed ID: 15732119
    [No Abstract] [Full Text] [Related]

  • 20. Review of Alexander disease: beyond the classical concept of leukodystrophy.
    Sawaishi Y.
    Brain Dev; 2009 Aug 28; 31(7):493-8. PubMed ID: 19386454
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.