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Journal Abstract Search

579 related items for PubMed ID: 33150406

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  • 3. Update on KMT2B-Related Dystonia.
    Zech M, Lam DD, Winkelmann J.
    Curr Neurol Neurosci Rep; 2019 Nov 25; 19(11):92. PubMed ID: 31768667
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  • 4. Deep brain stimulation for the treatment of childhood dystonic cerebral palsy.
    Keen JR, Przekop A, Olaya JE, Zouros A, Hsu FP.
    J Neurosurg Pediatr; 2014 Dec 25; 14(6):585-93. PubMed ID: 25325412
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  • 5. 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 25; 77():76-82. PubMed ID: 32634684
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  • 6. Long-Term Outcomes of Bilateral Pallidal Deep Brain Stimulation for X-Linked Dystonia and Parkinsonism.
    Kilbane C, Witt J, Galifianakis NB, Glass GA, Volz M, Heath S, Starr PA, Ostrem JL.
    Stereotact Funct Neurosurg; 2018 Aug 25; 96(5):320-326. PubMed ID: 30481788
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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 25; 52():55-61. PubMed ID: 29653907
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  • 10. Deep Brain Stimulation for GNAO1-Associated Dystonia: A Systematic Review and Meta-Analysis.
    Decraene B, Smeets S, Remans D, Ortibus E, Vandenberghe W, Nuttin B, Theys T, De Vloo P.
    Neuromodulation; 2024 Apr 25; 27(3):440-446. PubMed ID: 37999699
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  • 11. Proportion of life lived with dystonia inversely correlates with response to pallidal deep brain stimulation in both primary and secondary childhood dystonia.
    Lumsden DE, Kaminska M, Gimeno H, Tustin K, Baker L, Perides S, Ashkan K, Selway R, Lin JP.
    Dev Med Child Neurol; 2013 Jun 25; 55(6):567-74. PubMed ID: 23452222
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  • 12. Pallidal deep brain stimulation for dystonia: a long term study.
    Meoni S, Fraix V, Castrioto A, Benabid AL, Seigneuret E, Vercueil L, Pollak P, Krack P, Chevrier E, Chabardes S, Moro E.
    J Neurol Neurosurg Psychiatry; 2017 Nov 25; 88(11):960-967. PubMed ID: 28972096
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  • 13. Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia.
    Zech M, Boesch S, Maier EM, Borggraefe I, Vill K, Laccone F, Pilshofer V, Ceballos-Baumann A, Alhaddad B, Berutti R, Poewe W, Haack TB, Haslinger B, Strom TM, Winkelmann J.
    Am J Hum Genet; 2016 Dec 01; 99(6):1377-1387. PubMed ID: 27839873
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  • 15. Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile.
    Ciolfi A, Foroutan A, Capuano A, Pedace L, Travaglini L, Pizzi S, Andreani M, Miele E, Invernizzi F, Reale C, Panteghini C, Iascone M, Niceta M, Gavrilova RH, Schultz-Rogers L, Agolini E, Bedeschi MF, Prontera P, Garibaldi M, Galosi S, Leuzzi V, Soliveri P, Olson RJ, Zorzi GS, Garavaglia BM, Tartaglia M, Sadikovic B.
    Clin Epigenetics; 2021 Aug 11; 13(1):157. PubMed ID: 34380541
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  • 16. A severe case of status dystonicus caused by a de novo KMT2B missense mutation.
    Nakamura S, Chinen Y, Satou K, Tokashiki T, Kumada S, Yanagi K, Kaname T, Naritomi K, Nakanishi K.
    Eur J Med Genet; 2020 Nov 11; 63(11):104057. PubMed ID: 32877735
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  • 17. Early-onset generalized dystonia caused by a new mutation in the KMT2B gene: Case report.
    Rangel YA, Espinosa E.
    Biomedica; 2022 Sep 02; 42(3):429-434. PubMed ID: 36122281
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  • 19. Early-onset oromandibular-laryngeal dystonia and Charlot gait: New phenotype of DYT-KMT2B.
    Brás A, Ribeiro JA, Sobral F, Moreira F, Morgadinho A, Januário C.
    Neurology; 2019 May 07; 92(19):919. PubMed ID: 31061210
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  • 20. GPi-DBS for KMT2B-Associated Dystonia: Systematic Review and Meta-Analysis.
    Rajan R, Garg K, Saini A, Radhakrishnan DM, Carecchio M, Bk B, Singh M, Srivastava AK.
    Mov Disord Clin Pract; 2022 Jan 07; 9(1):31-37. PubMed ID: 35005062
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