Genetic updates on paroxysmal dyskinesias-Reference-Cited by-同舟云学术

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Genetic updates on paroxysmal dyskinesias

Published:2021-04 Issue:4 Volume:128 Page:447-471
ISSN:0300-9564
Container-title:Journal of Neural Transmission
language:en
Short-container-title:J Neural Transm

Author:

Liao James Y.,Salles Philippe A.,Shuaib Umar A.,Fernandez Hubert H.

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Psychiatry and Mental health,Clinical Neurology,Neurology

Link

https://link.springer.com/content/pdf/10.1007/s00702-021-02335-x.pdf

Reference163 articles.

1. Ahn H, Ko TS (2020) The genetic relationship between paroxysmal movement disorders and epilepsy. Ann Child Neurol 28(3): 76–87. https://doi.org/10.26815/acn.2020.00073

2. Anheim M, Maillart E, Vuillaumier-Barrot S, Flamand-Rouvière C, Pineau F, Ewenczyk C, Riant F, Apartis E, Roze E (2011) Excellent response to acetazolamide in a case of paroxysmal dyskinesias due to GLUT1-deficiency. J Neurol 258(2):316–317. https://doi.org/10.1007/s00415-010-5702-5

3. Anık A, Kersseboom S, Demir K, Catlı G, Yiş U, Böber E, van Mullem A et al (2014) Psychomotor retardation caused by a defective thyroid hormone transporter: report of two families with different MCT8 mutations. Hormone Res Paed 82(4):261–271. https://doi.org/10.1159/000365191

4. Bailey CS, Moldenhauer HJ, Park SM, Keros S, Meredith AL (2019) KCNMA1-linked channelopathy. J Gen Physiol 151(10):1173–1189. https://doi.org/10.1085/jgp.201912457

5. Bar-Peled L, Chantranupong L, Cherniack AD, Chen WW, Ottina KA, Grabiner BC, Spear ED, Carter SL, Meyerson M, Sabatini DM (2013) A tumor suppressor complex with GAP activity for the Rag GTPases that signal amino acid sufficiency to MTORC1. Science 340(6136):1100–1106. https://doi.org/10.1126/science.1232044

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