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Journal Abstract Search

351 related items for PubMed ID: 23812641

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  • 2. 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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  • 3. Spastin mutation screening in Chinese patients with pure hereditary spastic paraplegia.
    Wei QQ, Chen Y, Zheng ZZ, Chen X, Huang R, Yang Y, Burgunder J, Shang HF.
    Parkinsonism Relat Disord; 2014 Aug 15; 20(8):845-9. PubMed ID: 24824479
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  • 4. 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 15; 263(8):1604-11. PubMed ID: 27260292
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  • 5. Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia.
    Battini R, Fogli A, Borghetti D, Michelucci A, Perazza S, Baldinotti F, Conidi ME, Ferreri MI, Simi P, Cioni G.
    Eur J Neurol; 2011 Jan 15; 18(1):150-7. PubMed ID: 20550563
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  • 8. 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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  • 9. [Hereditary spastic paraplegia type 4 (SPG4): clinical and molecular-genetic characteristics].
    Rudenskaia GE, Sermiagina IG, Illarioshkin SN, Sidorova OP, Fedotov VP, Poliakov AV.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2010 Oct 15; 110(6):12-9. PubMed ID: 20559269
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  • 12. 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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  • 15. 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 08; 61(10):845-850. PubMed ID: 27334366
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  • 16. SPAST mutations in Australian patients with hereditary spastic paraplegia.
    Vandebona H, Kerr NP, Liang C, Sue CM.
    Intern Med J; 2012 Dec 08; 42(12):1342-7. PubMed ID: 23252998
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  • 19. Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia.
    Chelban V, Tucci A, Lynch DS, Polke JM, Santos L, Jonvik H, Groppa S, Wood NW, Houlden H.
    J Neurol Neurosurg Psychiatry; 2017 Aug 08; 88(8):681-687. PubMed ID: 28572275
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