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Journal Abstract Search

190 related items for PubMed ID: 22203332

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  • 2. 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. 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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  • 9. 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 15; 111(7):380-5. PubMed ID: 22817815
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  • 13. High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia.
    Lan MY, Chang YY, Yeh TH, Lai SC, Liou CW, Kuo HC, Wu YR, Lyu RK, Hung JW, Chang YC, Lu CS.
    BMC Neurol; 2014 Nov 25; 14():216. PubMed ID: 25421405
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  • 14. Alu-specific microhomology-mediated deletion of the final exon of SPAST in three unrelated subjects with hereditary spastic paraplegia.
    Boone PM, Liu P, Zhang F, Carvalho CM, Towne CF, Batish SD, Lupski JR.
    Genet Med; 2011 Jun 25; 13(6):582-92. PubMed ID: 21659953
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  • 15. 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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  • 18. 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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  • 20. Copy number variations in SPAST and ATL1 are rare among Brazilians.
    Fussiger H, Pereira BLDS, Padilha JPD, Donis KC, Rare-Genomes Project ConsortiumHospital Israelita Albert Einstein, São Paulo, Brazil., Siebert M, Brusius-Facchin AC, Baldo G, Saute JAM.
    Clin Genet; 2023 May 15; 103(5):580-584. PubMed ID: 36537231
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