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Journal Abstract Search

252 related items for PubMed ID: 23033504

  • 1. 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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  • 4. [Clinical polymorphism and genetic heterogeneity of hereditary spastic ataxia].
    Dadali EL, Illarioshkin SN, Markova ED, Ivanova-Smolenskaia IA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1992 Oct 02; 92(4):10-3. PubMed ID: 1333696
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  • 6. 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 02; 26(12):1585-9. PubMed ID: 21745802
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  • 8. Clinical presentation and early evolution of spastic ataxia of Charlevoix-Saguenay.
    Duquette A, Brais B, Bouchard JP, Mathieu J.
    Mov Disord; 2013 Dec 02; 28(14):2011-4. PubMed ID: 23913799
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  • 12. Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families.
    Gücüyener K, Ozgül K, Paternotte C, Erdem H, Prud'homme JF, Ozgüç M, Topaloğlu H.
    Neuropediatrics; 2001 Jun 02; 32(3):142-6. PubMed ID: 11521210
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  • 13. Genetic cerebellar ataxias.
    Storey E.
    Semin Neurol; 2014 Jul 02; 34(3):280-92. PubMed ID: 25192506
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  • 14. Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.
    Grieco GS, Malandrini A, Comanducci G, Leuzzi V, Valoppi M, Tessa A, Palmeri S, Benedetti L, Pierallini A, Gambelli S, Federico A, Pierelli F, Bertini E, Casali C, Santorelli FM.
    Neurology; 2004 Jan 13; 62(1):103-6. PubMed ID: 14718707
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  • 16. Retinal and pontine striations: neurodiagnostic signs of autosomal recessive spastic ataxia of Charlevoix-Saguenay.
    Leavitt JA, Singer W, Brown WL, Pulido JS, Brodsky MC.
    J Neuroophthalmol; 2014 Dec 13; 34(4):369-71. PubMed ID: 25237835
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  • 17. Optical coherence tomography in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
    Parkinson MH, Bartmann AP, Clayton LMS, Nethisinghe S, Pfundt R, Chapple JP, Reilly MM, Manji H, Wood NJ, Bremner F, Giunti P.
    Brain; 2018 Apr 01; 141(4):989-999. PubMed ID: 29538656
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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 01; 61():97-103. PubMed ID: 8421971
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