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Journal Abstract Search

167 related items for PubMed ID: 29907907

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  • 2. A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings.
    Polymeris AA, Tessa A, Anagnostopoulou K, Rubegni A, Galatolo D, Dinopoulos A, Gika AD, Youroukos S, Skouteli E, Santorelli FM, Pons R.
    J Neurol; 2016 Aug; 263(8):1604-11. PubMed ID: 27260292
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  • 3. Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.
    Elert-Dobkowska E, Stepniak I, Krysa W, Rajkiewicz M, Rakowicz M, Sobanska A, Rudzinska M, Wasielewska A, Pilch J, Kubalska J, Lipczynska-Lojkowska W, Kulczycki J, Kurdziel K, Sikorska A, Beetz C, Zaremba J, Sulek A.
    J Neurol Sci; 2015 Dec 15; 359(1-2):35-9. PubMed ID: 26671083
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  • 4. Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia.
    Kadnikova VA, Rudenskaya GE, Stepanova AA, Sermyagina IG, Ryzhkova OP.
    Sci Rep; 2019 Oct 08; 9(1):14412. PubMed ID: 31594988
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  • 5. Genetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegia.
    Lu X, Cen Z, Xie F, Ouyang Z, Zhang B, Zhao G, Luo W.
    J Neurol Sci; 2014 Dec 15; 347(1-2):368-71. PubMed ID: 25454648
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  • 6. ATL1 and REEP1 mutations in hereditary and sporadic upper motor neuron syndromes.
    de Bot ST, Veldink JH, Vermeer S, Mensenkamp AR, Brugman F, Scheffer H, van den Berg LH, Kremer HP, Kamsteeg EJ, van de Warrenburg BP.
    J Neurol; 2013 Mar 15; 260(3):869-75. PubMed ID: 23108492
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  • 9. Anticipation Can Be More Common in Hereditary Spastic Paraplegia with SPAST Mutations Than It Appears.
    Hashemi SS, Hajati R, Davarzani A, Rohani M, DanaeeFard F, Rahimi Bidgoli MM, Fatehi F, Kariminejad A, Najmabadi H, Nafissi S, Alavi A.
    Can J Neurol Sci; 2022 Sep 15; 49(5):651-661. PubMed ID: 34353391
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  • 10. Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.
    Balicza P, Grosz Z, Gonzalez MA, Bencsik R, Pentelenyi K, Gal A, Varga E, Klivenyi P, Koller J, Züchner S, Molnar JM.
    J Neurol Sci; 2016 May 15; 364():116-21. PubMed ID: 27084228
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  • 14. Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations.
    McMonagle P, Byrne PC, Fitzgerald B, Webb S, Parfrey NA, Hutchinson M.
    Neurology; 2000 Dec 26; 55(12):1794-800. PubMed ID: 11134375
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  • 16. Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey.
    Akçakaya NH, Özeş Ak B, Gonzalez MA, Züchner S, Battaloğlu E, Parman Y.
    Neurol Neurochir Pol; 2020 Dec 26; 54(2):176-184. PubMed ID: 32242913
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  • 19. Novel mutations in the SPAST gene cause hereditary spastic paraplegia.
    Zhu Z, Zhang C, Zhao G, Liu Q, Zhong P, Zhang M, Tang W, Zhan F, Tian W, Wang Y, Yin K, Huang X, Jiang J, Liu X, Liu S, Zhou H, Luan X, Tang H, Wang Y, Chen S, Cao L.
    Parkinsonism Relat Disord; 2019 Dec 26; 69():125-133. PubMed ID: 31751864
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