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Journal Abstract Search

212 related items for PubMed ID: 20214791

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  • 4. SPAST mutation spectrum and familial occurrence among Czech patients with pure hereditary spastic paraplegia.
    Mészárosová AU, Putzová M, Čermáková M, Vávrová D, Doležalová K, Smetanová I, Stejskal D, Beetz C, Seeman P.
    J Hum Genet; 2016 Oct; 61(10):845-850. PubMed ID: 27334366
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  • 5. Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia.
    Park H, Kang SH, Park S, Kim SY, Seo SH, Lee SJ, Lee JA, Cho SI, Sung JJ, Lee KW, Kim JY, Park SS, Seong MW.
    J Neurol Sci; 2015 Oct 15; 357(1-2):167-72. PubMed ID: 26208798
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  • 6. High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia.
    Beetz C, Nygren AO, Schickel J, Auer-Grumbach M, Bürk K, Heide G, Kassubek J, Klimpe S, Klopstock T, Kreuz F, Otto S, Schüle R, Schöls L, Sperfeld AD, Witte OW, Deufel T.
    Neurology; 2006 Dec 12; 67(11):1926-30. PubMed ID: 17035675
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  • 8. Clinical and genetic analysis of four Taiwanese families with autosomal dominant hereditary spastic paraplegia.
    Lan MY, Fu SC, Chang YY, Wu-Chou YH, Lai SC, Chen RS, Lu CS.
    J Formos Med Assoc; 2012 Jul 12; 111(7):380-5. PubMed ID: 22817815
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  • 11. Exon 8-17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: a case report and literature review.
    Wang K, Zhao G.
    J Neurol Sci; 2015 Oct 15; 357(1-2):282-4. PubMed ID: 26165777
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  • 12. 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 15; 69():125-133. PubMed ID: 31751864
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  • 13. Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.
    de Bot ST, van den Elzen RT, Mensenkamp AR, Schelhaas HJ, Willemsen MA, Knoers NV, Kremer HP, van de Warrenburg BP, Scheffer H.
    J Neurol Neurosurg Psychiatry; 2010 Oct 15; 81(10):1073-8. PubMed ID: 20562464
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  • 14. 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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  • 19. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.
    Alvarez V, Sánchez-Ferrero E, Beetz C, Díaz M, Alonso B, Corao AI, Gámez J, Esteban J, Gonzalo JF, Pascual-Pascual SI, López de Munain A, Moris G, Ribacoba R, Márquez C, Rosell J, Marín R, García-Barcina MJ, Del Castillo E, Benito C, Coto E, Group for the Study of the Genetics of Spastic Paraplegia.
    BMC Neurol; 2010 Oct 08; 10():89. PubMed ID: 20932283
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  • 20. 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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