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465 related items for PubMed ID: 25341883

  • 1. Mutation and clinical characteristics of autosomal-dominant hereditary spastic paraplegias in China.
    Luo Y, Chen C, Zhan Z, Wang Y, Du J, Hu Z, Liao X, Zhao G, Wang J, Yan X, Jiang H, Pan Q, Xia K, Tang B, Shen L.
    Neurodegener Dis; 2014; 14(4):176-83. PubMed ID: 25341883
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia.
    Dürr A, Camuzat A, Colin E, Tallaksen C, Hannequin D, Coutinho P, Fontaine B, Rossi A, Gil R, Rousselle C, Ruberg M, Stevanin G, Brice A.
    Arch Neurol; 2004 Dec 15; 61(12):1867-72. PubMed ID: 15596607
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.
    Sauter SM, Engel W, Neumann LM, Kunze J, Neesen J.
    Hum Mutat; 2004 Jan 15; 23(1):98. PubMed ID: 14695538
    [Abstract] [Full Text] [Related]

  • 6. Hereditary spastic paraplegia: identification of an SPG3A gene mutation in a Chinese family.
    Chan KY, Ching CK, Mak CM, Lam CW, Chan AY.
    Hong Kong Med J; 2009 Aug 15; 15(4):304-7. PubMed ID: 19652243
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.
    Finsterer J, Löscher W, Quasthoff S, Wanschitz J, Auer-Grumbach M, Stevanin G.
    J Neurol Sci; 2012 Jul 15; 318(1-2):1-18. PubMed ID: 22554690
    [Abstract] [Full Text] [Related]

  • 11. [Hereditary spastic paraplegia type 4 (SPG4) in Russian patients].
    Rudenskaya GE, Kadnikova VA, Sidorova OP, Beetz C, Illarioshkin SN, Dadaly EL, Proskokova TN, Ryzhkova OP.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2019 Jul 15; 119(11):11-20. PubMed ID: 31851166
    [Abstract] [Full Text] [Related]

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

  • 13. 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]

  • 14. Novel mutation in the ATL1 with autosomal dominant hereditary spastic paraplegia presented as dysautonomia.
    Shin JW, Jung KH, Lee ST, Moon J, Seong MW, Park SS, Lee SK, Chu K.
    Auton Neurosci; 2014 Oct 08; 185():141-3. PubMed ID: 24969372
    [Abstract] [Full Text] [Related]

  • 15. 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 08; 49(5):651-661. PubMed ID: 34353391
    [Abstract] [Full Text] [Related]

  • 16. Clinical and genetic characteristics in a Chinese cohort of complex spastic paraplegia type 4.
    Yao L, Cao Y, Zhang C, Huang X, Tian W, Cao L.
    Clin Genet; 2024 Jul 08; 106(1):56-65. PubMed ID: 38403837
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Autosomal dominant spastic paraplegias: a review of 89 families resulting from a portuguese survey.
    Loureiro JL, Brandão E, Ruano L, Brandão AF, Lopes AM, Thieleke-Matos C, Miller-Fleming L, Cruz VT, Barbosa M, Silveira I, Stevanin G, Pinto-Basto J, Sequeiros J, Alonso I, Coutinho P.
    JAMA Neurol; 2013 Apr 15; 70(4):481-7. PubMed ID: 23400676
    [Abstract] [Full Text] [Related]

  • 19. Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China.
    Dong EL, Wang C, Wu S, Lu YQ, Lin XH, Su HZ, Zhao M, He J, Ma LX, Wang N, Chen WJ, Lin X.
    Mol Neurodegener; 2018 Jul 06; 13(1):36. PubMed ID: 29980238
    [Abstract] [Full Text] [Related]

  • 20. The investigation of genetic and clinical features in patients with hereditary spastic paraplegia in central-Southern China.
    Wang C, Zhang YJ, Xu CH, Li D, Liu ZJ, Wu Y.
    Mol Genet Genomic Med; 2021 May 06; 9(5):e1627. PubMed ID: 33638609
    [Abstract] [Full Text] [Related]

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