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Journal Abstract Search

153 related items for PubMed ID: 32877735

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  • 4. [A case of generalized dystonia DYT28 with a novel de novo mutation in the KMT2B gene].
    Hara K, Ouchi H, Hamanaka K, Miyatake S, Matsumoto N.
    Rinsho Shinkeigaku; 2022 Nov 26; 62(11):856-859. PubMed ID: 36288966
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  • 8. Clinical phenotypes, genotypes and treatment in Chinese dystonia patients with KMT2B variants.
    Li XY, Dai LF, Wan XH, Guo Y, Dai Y, Li SL, Fang F, Wang XH, Zhang WH, Liu TH, Xie ZH, Fang T, Wang L, Ding CH.
    Parkinsonism Relat Disord; 2020 Aug 26; 77():76-82. PubMed ID: 32634684
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  • 9. Phenotype variability and allelic heterogeneity in KMT2B-Associated disease.
    Kawarai T, Miyamoto R, Nakagawa E, Koichihara R, Sakamoto T, Mure H, Morigaki R, Koizumi H, Oki R, Montecchiani C, Caltagirone C, Orlacchio A, Hattori A, Mashimo H, Izumi Y, Mezaki T, Kumada S, Taniguchi M, Yokochi F, Saitoh S, Goto S, Kaji R.
    Parkinsonism Relat Disord; 2018 Jul 26; 52():55-61. PubMed ID: 29653907
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  • 10. Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study.
    Carecchio M, Invernizzi F, Gonzàlez-Latapi P, Panteghini C, Zorzi G, Romito L, Leuzzi V, Galosi S, Reale C, Zibordi F, Joseph AP, Topf M, Piano C, Bentivoglio AR, Girotti F, Morana P, Morana B, Kurian MA, Garavaglia B, Mencacci NE, Lubbe SJ, Nardocci N.
    Mov Disord; 2019 Oct 26; 34(10):1516-1527. PubMed ID: 31216378
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  • 17. Child Neurology: KMT2B-Related Dystonia in a Young Child With Worsening Gait Abnormality.
    Schuberth K, Ramani PK, Beemarajan E, Veerapandiyan A.
    Neurology; 2023 Aug 15; 101(7):328-332. PubMed ID: 37041082
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  • 20. Dystonic Tremor in Adult-onset DYT-KMT2B.
    Shimazaki R, Ikezawa J, Okiyama R, Azuma K, Akagawa H, Takahashi K.
    Intern Med; 2022 Aug 01; 61(15):2357-2360. PubMed ID: 35022352
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