Varied phenotypic spectrum presenting of paroxysmal exercise–induced dyskinesia: a Turkish family with SLC2A1 mutation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-021-05466-x.pdf
Reference13 articles.
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2. Gardiner AR, Jaffer F, Dale RC, Labrum R, Erro R, Meyer E, Xiromerisiou G, Stamelou M, Walker M, Kullmann D, Warner T, Jarman P, Hanna M, Kurian MA, Bhatia KP, Houlden H (2015) The clinical and genetic heterogeneity of paroxysmal dyskinesias. Brain 138(Pt 12):35673580. https://doi.org/10.1093/brain/awv310
3. Kim SY, Lee JS, Kim WJ, Kim H, Choi SA, Lim BC, Kim KJ, Chae JH (2018) Paroxysmal dyskinesia in children: from genes to the clinic. J Clin Neurol 14(4):492–497. https://doi.org/10.3988/jcn.2018.14.4.492
4. Tang M, Park SH, De Vivo DC, Monani UR (2019) Therapeutic strategies for glucose transporter 1 deficiency syndrome. Ann Clin Transl Neurol 6(9):1923–1932. https://doi.org/10.1002/acn3.50881
5. Manso-Calderon R (2019) Clinical features and treatment in the spectrum of paroxysmal dyskinesias: an observational study in South-West Castilla y Leon Spain. Neurol Res Int 2019:4191796. https://doi.org/10.1155/2019/4191796
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