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322 related items for PubMed ID: 26208798

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Mutation analysis of four Chinese families with pure hereditary spastic paraplegia: pseudo- X-linked dominant inheritance and male lethality due to a novel ATL1 mutation.
    Zhao N, Sui Y, Li XF, Liu W, Lu YP, Feng WH, Ma C, Wang YW, Bao HX, Huang F, Wang H, Yi DX, Han WT, Jiang M.
    Genet Mol Res; 2015 Nov 23; 14(4):14690-7. PubMed ID: 26600529
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Disease-Causing Variants in the ATL1 Gene Are a Rare Cause of Hereditary Spastic Paraplegia among Czech Patients.
    Mészárosová AU, Grečmalová D, Brázdilová M, Dvořáčková N, Kalina Z, Čermáková M, Vávrová D, Smetanová I, Staněk D, Seeman P.
    Ann Hum Genet; 2017 Nov 15; 81(6):249-257. PubMed ID: 28736820
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia.
    Svenstrup K, Bross P, Koefoed P, Hjermind LE, Eiberg H, Born AP, Vissing J, Gyllenborg J, Nørremølle A, Hasholt L, Nielsen JE.
    J Neurol Sci; 2009 Sep 15; 284(1-2):90-5. PubMed ID: 19423133
    [Abstract] [Full Text] [Related]

  • 11. Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals.
    Sulek A, Elert E, Rajkiewicz M, Zdzienicka E, Stepniak I, Krysa W, Zaremba J.
    Neurol Sci; 2013 Feb 15; 34(2):239-42. PubMed ID: 22203332
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia.
    Kim TH, Lee JH, Park YE, Shin JH, Nam TS, Kim HS, Jang HJ, Semenov A, Kim SJ, Kim DS.
    J Clin Neurol; 2014 Jul 15; 10(3):257-61. PubMed ID: 25045380
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 15. Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients.
    Lu C, Li LX, Dong HL, Wei Q, Liu ZJ, Ni W, Gitler AD, Wu ZY.
    J Mol Med (Berl); 2018 Jul 15; 96(7):701-712. PubMed ID: 29934652
    [Abstract] [Full Text] [Related]

  • 16. A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia.
    Yu W, Jin H, Deng J, Nan D, Huang Y.
    BMC Med Genet; 2020 Jun 03; 21(1):123. PubMed ID: 32493220
    [Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. Four mutations of the spastin gene in Japanese families with spastic paraplegia.
    Basri R, Yabe I, Soma H, Takei A, Nishimura H, Machino Y, Kokubo Y, Kosugi M, Okada R, Yukitake M, Tachibana H, Kuroda Y, Kuzuhara S, Sasaki H.
    J Hum Genet; 2006 Oct 15; 51(8):711-715. PubMed ID: 16788734
    [Abstract] [Full Text] [Related]

  • 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 15; 69():125-133. PubMed ID: 31751864
    [Abstract] [Full Text] [Related]

  • 20. SPAST mutations in Australian patients with hereditary spastic paraplegia.
    Vandebona H, Kerr NP, Liang C, Sue CM.
    Intern Med J; 2012 Dec 15; 42(12):1342-7. PubMed ID: 23252998
    [Abstract] [Full Text] [Related]

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