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Year | Number of Results |
---|---|
2020 | 1 |
2021 | 3 |
2022 | 1 |
2024 | 0 |
PubMed (cited) for id: 619687
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Heterozygous EIF2AK2 Variant Causes Adolescence-Onset Generalized Dystonia Partially Responsive to DBS.
Mov Disord Clin Pract. 2021 Nov 21;9(2):268-271. doi: 10.1002/mdc3.13371. eCollection 2022 Feb.
Mov Disord Clin Pract. 2021.
PMID: 35146068
Free PMC article.
No abstract available.
A Recurrent EIF2AK2 Missense Variant Causes Autosomal-Dominant Isolated Dystonia.
Musacchio T, Zech M, Reich MM, Winkelmann J, Volkmann J.
Musacchio T, et al.
Ann Neurol. 2021 Jun;89(6):1257-1258. doi: 10.1002/ana.26081. Epub 2021 May 4.
Ann Neurol. 2021.
PMID: 33866603
No abstract available.
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EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia.
Kuipers DJS, Mandemakers W, Lu CS, Olgiati S, Breedveld GJ, Fevga C, Tadic V, Carecchio M, Osterman B, Sagi-Dain L, Wu-Chou YH, Chen CC, Chang HC, Wu SL, Yeh TH, Weng YH, Elia AE, Panteghini C, Marotta N, Pauly MG, Kühn AA, Volkmann J, Lace B, Meijer IA, Kandaswamy K, Quadri M, Garavaglia B, Lohmann K, Bauer P, Mencacci NE, Lubbe SJ, Klein C, Bertoli-Avella AM, Bonifati V.
Kuipers DJS, et al.
Ann Neurol. 2021 Mar;89(3):485-497. doi: 10.1002/ana.25973. Epub 2020 Dec 15.
Ann Neurol. 2021.
PMID: 33236446
Free PMC article.
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