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Journal Abstract Search

732 related items for PubMed ID: 23707147

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  • 4. Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study.
    Diallo A, Jacobi H, Cook A, Labrum R, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sobanska A, Sulek A, Schmitz-Hübsch T, Schöls L, Hengel H, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Boesch S, Pandolfo M, Schulz JB, Bauer P, Giunti P, Kang JS, Klockgether T, Tezenas du Montcel S.
    Lancet Neurol; 2018 Apr; 17(4):327-334. PubMed ID: 29553382
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  • 5. Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
    Schulz JB, Borkert J, Wolf S, Schmitz-Hübsch T, Rakowicz M, Mariotti C, Schöls L, Timmann D, van de Warrenburg B, Dürr A, Pandolfo M, Kang JS, Mandly AG, Nägele T, Grisoli M, Boguslawska R, Bauer P, Klockgether T, Hauser TK.
    Neuroimage; 2010 Jan 01; 49(1):158-68. PubMed ID: 19631275
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  • 10. Disease progression of spinocerebellar ataxia types 1, 2, 3 and 6 before and after ataxia onset.
    Jacobi H, Schaprian T, Schmitz-Hübsch T, Schmid M, Klockgether T, EUROSCA and RISCA Study Groups.
    Ann Clin Transl Neurol; 2023 Oct 01; 10(10):1833-1843. PubMed ID: 37592453
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  • 15. Longitudinal Changes of Clinical, Imaging, and Fluid Biomarkers in Preataxic and Early Ataxic Spinocerebellar Ataxia Type 2 and 7 Carriers.
    Coarelli G, Dubec-Fleury C, Petit E, Sayah S, Fischer C, Nassisi M, Gatignol P, Dorgham K, Daghsen L, Daye P, Cunha P, Kacher R, Hilab R, Hurmic H, Lamazière A, Lamy JC, Welter ML, Chupin M, Mangin JF, Lane R, Gaymard B, Pouget P, Audo I, Brice A, Tezenas du Montcel S, Durr A.
    Neurology; 2024 Sep 10; 103(5):e209749. PubMed ID: 39133883
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  • 17. [Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
    Rakowicz M, Zdzienicka E, Poniatowska R, Waliniowska E, Sułek A, Jakubowska T, Niedzielska K, Rola R, Wierzbicka A, Hoffman-Zacharska D, Głazowski C, Jakubczyk T, Niewiadomska M, Zaremba J.
    Neurol Neurochir Pol; 2005 Sep 10; 39(4):263-275. PubMed ID: 16096942
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  • 18. Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
    Reetz K, Costa AS, Mirzazade S, Lehmann A, Juzek A, Rakowicz M, Boguslawska R, Schöls L, Linnemann C, Mariotti C, Grisoli M, Dürr A, van de Warrenburg BP, Timmann D, Pandolfo M, Bauer P, Jacobi H, Hauser TK, Klockgether T, Schulz JB, axia Study Group Investigators.
    Brain; 2013 Mar 10; 136(Pt 3):905-17. PubMed ID: 23423669
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