These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

218 related items for PubMed ID: 25045380

  • 1. 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; 10(3):257-61. PubMed ID: 25045380
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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]

  • 7. 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]

  • 8.
    ; . PubMed ID:
    [No 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. 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]

  • 11. ATL1 and REEP1 mutations in hereditary and sporadic upper motor neuron syndromes.
    de Bot ST, Veldink JH, Vermeer S, Mensenkamp AR, Brugman F, Scheffer H, van den Berg LH, Kremer HP, Kamsteeg EJ, van de Warrenburg BP.
    J Neurol; 2013 Mar 08; 260(3):869-75. PubMed ID: 23108492
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia.
    Perić S, Marković V, Candayan A, De Vriendt E, Momčilović N, Savić A, Dragašević-Mišković N, Svetel M, Stević Z, Božović I, Mesaroš Š, Drulović J, Basta I, Petrović I, Tamaš O, Mijajlović M, Novaković I, Sokić D, Jordanova A.
    Cells; 2022 Sep 08; 11(18):. PubMed ID: 36139378
    [Abstract] [Full Text] [Related]

  • 15. Three novel mutations in 20 patients with hereditary spastic paraparesis.
    Duz MB, Dasdemir S, Kalayci Yigin A, Akalin MA, Seven M.
    Neurol Sci; 2018 Sep 08; 39(9):1551-1557. PubMed ID: 29907907
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. [A novel mutation of SPAST gene in a hereditary spastic paraplegia type 4 family].
    Zhang LP, Wang YF.
    Zhonghua Nei Ke Za Zhi; 2022 Dec 01; 61(12):1343-1350. PubMed ID: 36456515
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.