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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

172 related items for PubMed ID: 32146693

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  • 22. SYNE1-ataxia: Novel genotypic and phenotypic findings.
    Indelicato E, Nachbauer W, Fauth C, Krabichler B, Schossig A, Eigentler A, Dichtl W, Wenning G, Wagner M, Fanciulli A, Janecke A, Boesch S.
    Parkinsonism Relat Disord; 2019 May; 62():210-214. PubMed ID: 30573412
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  • 24. Spastic ataxia with eye-of-the-tiger-like sign in 4 siblings due to novel compound heterozygous AFG3L2 mutation.
    Calandra CR, Buda G, Vishnopolska SA, Oliveri J, Olivieri FA, Pérez Millán MI, Biagioli G, Miquelini LA, Pellene AL, Marti MA.
    Parkinsonism Relat Disord; 2020 Apr; 73():52-54. PubMed ID: 32248051
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  • 33. Hereditary Myelopathies.
    Hedera P.
    Continuum (Minneap Minn); 2018 Apr; 24(2, Spinal Cord Disorders):523-550. PubMed ID: 29613898
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  • 34. A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.
    Johnson JO, Stevanin G, van de Leemput J, Hernandez DG, Arepalli S, Forlani S, Zonozi R, Gibbs JR, Brice A, Durr A, Singleton AB.
    Mov Disord; 2015 Feb; 30(2):262-6. PubMed ID: 25545641
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  • 35. Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype.
    Mahale R, Padmanabha H, Mailankody P, Pavagada M.
    Acta Neurol Belg; 2024 Jun; 124(3):1049-1050. PubMed ID: 37976028
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