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

99 related items for PubMed ID: 15514925

  • 21. Malaysian siblings with friedreich ataxia and chorea: a novel deletion in the frataxin gene.
    Spacey SD, Szczygielski BI, Young SP, Hukin J, Selby K, Snutch TP.
    Can J Neurol Sci; 2004 Aug; 31(3):383-6. PubMed ID: 15376485
    [Abstract] [Full Text] [Related]

  • 22. A mild case of Friedreich ataxia: lymphocyte and sural nerve analysis for GAA repeat length reveals somatic mosaicism.
    Machkhas H, Bidichandani SI, Patel PI, Harati Y.
    Muscle Nerve; 1998 Mar; 21(3):390-3. PubMed ID: 9486868
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 25. Friedreich ataxia with minimal GAA expansion presenting as adult-onset spastic ataxia.
    Berciano J, Mateo I, De Pablos C, Polo JM, Combarros O.
    J Neurol Sci; 2002 Feb 15; 194(1):75-82. PubMed ID: 11809170
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. [Late onset Friedreich ataxia: clinical description of a family in Argentina].
    Pérez Akly M, Alvarez F.
    Medicina (B Aires); 2013 Feb 15; 73(5):457-60. PubMed ID: 24152405
    [Abstract] [Full Text] [Related]

  • 29. Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia.
    Ragno M, De Michele G, Cavalcanti F, Pianese L, Monticelli A, Curatola L, Bollettini F, Cocozza S, Caruso G, Santoro L, Filla A.
    Neurology; 1997 Dec 15; 49(6):1617-20. PubMed ID: 9409356
    [Abstract] [Full Text] [Related]

  • 30. Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up.
    Ribaï P, Pousset F, Tanguy ML, Rivaud-Pechoux S, Le Ber I, Gasparini F, Charles P, Béraud AS, Schmitt M, Koenig M, Mallet A, Brice A, Dürr A.
    Arch Neurol; 2007 Apr 15; 64(4):558-64. PubMed ID: 17420319
    [Abstract] [Full Text] [Related]

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

  • 32. Hereditary spastic paraplegia.
    Roşulescu E, Stănoiu C, Buteică E, Stănoiu B, Burada F, Zăvăleanu M.
    Rom J Morphol Embryol; 2009 Apr 15; 50(2):299-303. PubMed ID: 19434327
    [Abstract] [Full Text] [Related]

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

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 37. Familial spastic paraplegia: a clinical and electrodiagnostic evaluation.
    Owens LA, Peterson CR, Burdick AB.
    Arch Phys Med Rehabil; 1982 Aug 15; 63(8):357-61. PubMed ID: 7115028
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 40. Coexistence of tuberous sclerosis and Friedreich ataxia.
    Walker M, Samii A, Bird T.
    J Neurol Sci; 2004 Jun 15; 221(1-2):91-3. PubMed ID: 15178220
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.