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Journal Abstract Search

231 related items for PubMed ID: 647499

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  • 3. Autosomal recessive spastic ataxia of Charlevoix-Saguenay: compound heterozygotes for nonsense mutations of the SACS gene.
    Narayanan V, Rice SG, Olfers SS, Sivakumar K.
    J Child Neurol; 2011 Dec; 26(12):1585-9. PubMed ID: 21745802
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  • 4. Electromyography and nerve conduction studies in Friedreich's ataxia and autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS).
    Bouchard JP, Barbeau A, Bouchard R, Bouchard RW.
    Can J Neurol Sci; 1979 May; 6(2):185-9. PubMed ID: 487308
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  • 5. Genetic epidemiology of autosomal recessive spastic ataxia of Charlevoix-Saguenay in northeastern Quebec.
    De Braekeleer M, Giasson F, Mathieu J, Roy M, Bouchard JP, Morgan K.
    Genet Epidemiol; 1993 May; 10(1):17-25. PubMed ID: 8472930
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  • 7. Reviewing the genetic causes of spastic-ataxias.
    de Bot ST, Willemsen MA, Vermeer S, Kremer HP, van de Warrenburg BP.
    Neurology; 2012 Oct 02; 79(14):1507-14. PubMed ID: 23033504
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  • 16. Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia.
    Kumar D, Blank CE.
    Indian Pediatr; 1989 Oct 02; 26(10):1014-9. PubMed ID: 2630444
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  • 17. [Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature].
    Anheim M, Chaigne D, Fleury M, Santorelli FM, De Sèze J, Durr A, Brice A, Koenig M, Tranchant C.
    Rev Neurol (Paris); 2008 Apr 02; 164(4):363-8. PubMed ID: 18439928
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  • 19. Clinical and molecular genetic studies on autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS).
    Richter A, Morgan K, Bouchard JP, Poirier J, Mercier J, Gosselin F, Melançon SB.
    Adv Neurol; 1993 Apr 02; 61():97-103. PubMed ID: 8421971
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