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Journal Abstract Search

261 related items for PubMed ID: 19040626

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  • 4. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum.
    Olmez A, Uyanik G, Ozgül RK, Gross C, Cirak S, Elibol B, Anlar B, Winner B, Hehr U, Topaloglu H, Winkler J.
    Neuropediatrics; 2006 Apr; 37(2):59-66. PubMed ID: 16773502
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  • 5. Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.
    Brockmann K, Simpson MA, Faber A, Bönnemann C, Crosby AH, Gärtner J.
    Neuropediatrics; 2005 Aug; 36(4):274-8. PubMed ID: 16138254
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  • 9. Autosomal recessive hereditary spastic paraparesis with thin corpus callosum; report of two sisters.
    Vucic S, Lye T, Dunn G, Corbett A.
    J Clin Neurosci; 2004 May; 11(4):427-30. PubMed ID: 15080965
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  • 12. Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum.
    Chen Q, Lui S, Wang JG, Ou-Yang L, Zhou D, Burgunder JM, Gong QY, Shang HF.
    Neurosci Lett; 2008 Aug 15; 441(1):21-4. PubMed ID: 18586399
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  • 14. "Ears of the Lynx" MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia.
    Pascual B, de Bot ST, Daniels MR, França MC, Toro C, Riverol M, Hedera P, Bassi MT, Bresolin N, van de Warrenburg BP, Kremer B, Nicolai J, Charles P, Xu J, Singh S, Patronas NJ, Fung SH, Gregory MD, Masdeu JC.
    AJNR Am J Neuroradiol; 2019 Jan 15; 40(1):199-203. PubMed ID: 30606727
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  • 16. Pattern reversal visual evoked potentials (prVEPs) in autosomal recessive hereditary spastic paraplegia with thin corpus callosum (ARHSPTCC) patients with SPG 11 mutations in Saudi Arabia, cross section hospital base study.
    Alfaidi N, Sobahy T, Ali Q, Al Said Y, Karim G, Khan H, Kurdi K, Cupler E.
    J Neurol Sci; 2022 Mar 15; 434():120144. PubMed ID: 35074613
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  • 19. Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.
    Shibasaki Y, Tanaka H, Iwabuchi K, Kawasaki S, Kondo H, Uekawa K, Ueda M, Kamiya T, Katayama Y, Nakamura A, Takashima H, Nakagawa M, Masuda M, Utsumi H, Nakamuro T, Tada K, Kurohara K, Inoue K, Koike F, Sakai T, Tsuji S, Kobayashi H.
    Ann Neurol; 2000 Jul 15; 48(1):108-12. PubMed ID: 10894224
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