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Journal Abstract Search

253 related items for PubMed ID: 26374131

  • 1.
    ; . PubMed ID:
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  • 2. 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; 263(8):1604-11. PubMed ID: 27260292
    [Abstract] [Full Text] [Related]

  • 3. Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegia.
    Kumar KR, Blair NF, Vandebona H, Liang C, Ng K, Sharpe DM, Grünewald A, Gölnitz U, Saviouk V, Rolfs A, Klein C, Sue CM.
    J Neurol; 2013 Oct; 260(10):2516-22. PubMed ID: 23812641
    [Abstract] [Full Text] [Related]

  • 4. Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families.
    Pashaei M, Davarzani A, Hajati R, Zamani B, Nafissi S, Larti F, Nilipour Y, Rohani M, Alavi A.
    J Neurogenet; 2021 Oct; 35(2):84-94. PubMed ID: 33771085
    [Abstract] [Full Text] [Related]

  • 5. Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.
    Méreaux JL, Banneau G, Papin M, Coarelli G, Valter R, Raymond L, Kol B, Ariste O, Parodi L, Tissier L, Mairey M, Ait Said S, Gautier C, Guillaud-Bataille M, French SPATAX clinical network, Forlani S, de la Grange P, Brice A, Vazza G, Durr A, Leguern E, Stevanin G.
    Brain; 2022 Apr 29; 145(3):1029-1037. PubMed ID: 34983064
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 15; 9(5):e1627. PubMed ID: 33638609
    [Abstract] [Full Text] [Related]

  • 8. Genetic, clinical and neuroimaging profiles of sporadic and autosomal recessive hereditary spastic paraplegia cases in Chinese.
    Dong Y, Li XY, Wang XL, Xu F, Wang ZJ, Song Y, Li Q, Lin R, Wang C.
    Neurosci Lett; 2021 Sep 14; 761():136108. PubMed ID: 34256108
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Clinical and molecular characterization of hereditary spastic paraplegia in a spanish Southern region.
    Carrasco Salas P, Martínez Fernández E, Méndez Del Barrio C, Serrano Mira A, Guerrero Moreno N, Royo I, Delgado M, Oropesa JM, Vázquez Rico I.
    Int J Neurosci; 2022 Aug 08; 132(8):767-777. PubMed ID: 33059505
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
    Goizet C, Boukhris A, Durr A, Beetz C, Truchetto J, Tesson C, Tsaousidou M, Forlani S, Guyant-Maréchal L, Fontaine B, Guimarães J, Isidor B, Chazouillères O, Wendum D, Grid D, Chevy F, Chinnery PF, Coutinho P, Azulay JP, Feki I, Mochel F, Wolf C, Mhiri C, Crosby A, Brice A, Stevanin G.
    Brain; 2009 Jun 15; 132(Pt 6):1589-600. PubMed ID: 19439420
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 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 03; 49(5):651-661. PubMed ID: 34353391
    [Abstract] [Full Text] [Related]

  • 16. Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes.
    Elert-Dobkowska E, Stepniak I, Krysa W, Ziora-Jakutowicz K, Rakowicz M, Sobanska A, Pilch J, Antczak-Marach D, Zaremba J, Sulek A.
    Neurogenetics; 2019 Mar 03; 20(1):27-38. PubMed ID: 30778698
    [Abstract] [Full Text] [Related]

  • 17. Novel deletion of SPAST in a Chinese family with hereditary spastic paraplegia.
    Feng Y, Ke X, Zhai M, Xin Q, Gong Y, Liu Q.
    Singapore Med J; 2013 May 03; 54(5):251-4. PubMed ID: 23716148
    [Abstract] [Full Text] [Related]

  • 18. Exome sequencing identifies novel compound heterozygous mutations in SPG11 that cause autosomal recessive hereditary spastic paraplegia.
    Zhao W, Zhu QY, Zhang JT, Liu H, Wang LJ, Chen ZQ, Guan LP, Huang XS, Yang L, Yu SY.
    J Neurol Sci; 2013 Dec 15; 335(1-2):112-7. PubMed ID: 24090761
    [Abstract] [Full Text] [Related]

  • 19. Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey.
    Akçakaya NH, Özeş Ak B, Gonzalez MA, Züchner S, Battaloğlu E, Parman Y.
    Neurol Neurochir Pol; 2020 Dec 15; 54(2):176-184. PubMed ID: 32242913
    [Abstract] [Full Text] [Related]

  • 20. A complex form of hereditary spastic paraplegia in three siblings due to somatic mosaicism for a novel SPAST mutation in the mother.
    Aulitzky A, Friedrich K, Gläser D, Gastl R, Kubisch C, Ludolph AC, Volk AE.
    J Neurol Sci; 2014 Dec 15; 347(1-2):352-5. PubMed ID: 25315759
    [Abstract] [Full Text] [Related]

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