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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2017 1
2018 1
2019 2
2020 2
2021 5
2022 10
2023 2

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20 results

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Page 1
Autoimmune neuromyotonia.
Comperat L, Pegat A, Honnorat J, Joubert B. Comperat L, et al. Among authors: pegat a. Curr Opin Neurol. 2022 Oct 1;35(5):597-603. doi: 10.1097/WCO.0000000000001104. Epub 2022 Aug 19. Curr Opin Neurol. 2022. PMID: 35989569 Review.
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy.
Jacquier A, Theuriet J, Fontaine F, Mosbach V, Lacoste N, Ribault S, Risson V, Carras J, Coudert L, Simonet T, Latour P, Stojkovic T, Piard J, Cosson A, Lesca G, Bouhour F, Allouche S, Puccio H, Pégat A, Schaeffer L. Jacquier A, et al. Among authors: pegat a. Brain. 2022 Dec 1:awac453. doi: 10.1093/brain/awac453. Online ahead of print. Brain. 2022. PMID: 36454683
Amyotrophic lateral sclerosis associated with a pathological expansion in the ATXN7 gene.
Cluse F, Bernard E, Strubi-Vuillaume I, Devos D, Mouzat K, Lumbroso S, Froment Tilikete C, Thobois S, Pegat A. Cluse F, et al. Among authors: pegat a. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Aug;23(5-6):470-472. doi: 10.1080/21678421.2021.1998537. Epub 2021 Dec 6. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34870541
"Myelitis migrans": A rare cause of treatable myelitis.
Jaulent P, Pegat A, Grosset-Janin C, Durand-Dubief F, Vukusic S, Marignier R. Jaulent P, et al. Among authors: pegat a. Rev Neurol (Paris). 2018 Dec;174(10):745-747. doi: 10.1016/j.neurol.2017.12.005. Epub 2018 Aug 22. Rev Neurol (Paris). 2018. PMID: 30143322 No abstract available.
20 results