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111 results

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Page 1
Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions.
Méreaux JL, Davoine CS, Pellerin D, Coarelli G, Coutelier M, Ewenczyk C, Monin ML, Anheim M, Le Ber I, Thobois S, Gobert F, Guillot-Noël L, Forlani S, Jornea L, Heinzmann A, Sangare A, Gaymard B, Guyant-Maréchal L, Charles P, Marelli C, Honnorat J, Degos B, Tison F, Sangla S, Simonetta-Moreau M, Salachas F, Tchikviladzé M, Castelnovo G, Mochel F, Klebe S, Castrioto A, Fenu S, Méneret A, Bourdain F, Wandzel M, Roth V, Bonnet C, Riant F, Stevanin G, Noël S, Fauret-Amsellem AL, Bahlo M, Lockhart PJ, Brais B, Renaud M, Brice A, Durr A. Méreaux JL, et al. Among authors: gaymard b. EBioMedicine. 2024 Jan;99:104931. doi: 10.1016/j.ebiom.2023.104931. Epub 2023 Dec 27. EBioMedicine. 2024. PMID: 38150853 Free PMC article.
Keep your eyes peeled for VPS16.
Desjardins C, Delorme C, Méneret A, Roze E, Gaymard B, Vidailhet M. Desjardins C, et al. Among authors: gaymard b. Parkinsonism Relat Disord. 2024 Mar;120:106005. doi: 10.1016/j.parkreldis.2024.106005. Epub 2024 Jan 11. Parkinsonism Relat Disord. 2024. PMID: 38232514 No abstract available.
Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia.
Wirth T, Roze E, Delvallée C, Trouillard O, Drouot N, Damier P, Boulay C, Bourgninaud M, Jegatheesan P, Sangare A, Forlani S, Gaymard B, Hervochon R, Navarro V, Calmels N, Schalk A, Tranchant C, Piton A, Méneret A, Anheim M. Wirth T, et al. Among authors: gaymard b. Mov Disord. 2024 Mar 4. doi: 10.1002/mds.29752. Online ahead of print. Mov Disord. 2024. PMID: 38436103
Eye movement abnormalities in neurodegenerative langerhans cell histiocytosis.
Autier L, Gaymard B, Bayen E, Del Cul A, Cohen-Aubart F, Martin-Duverneuil N, Haroche J, Mokhtari K, Héritier S, Donadieu J, Hoang-Xuan K, Idbaih A. Autier L, et al. Among authors: gaymard b. Neurol Sci. 2022 Nov;43(11):6539-6546. doi: 10.1007/s10072-022-06180-y. Epub 2022 Jun 28. Neurol Sci. 2022. PMID: 35760933
Motor neuron pathology in CANVAS due to RFC1 expansions.
Huin V, Coarelli G, Guemy C, Boluda S, Debs R, Mochel F, Stojkovic T, Grabli D, Maisonobe T, Gaymard B, Lenglet T, Tard C, Davion JB, Sablonnière B, Monin ML, Ewenczyk C, Viala K, Charles P, Le Ber I, Reilly MM, Houlden H, Cortese A, Seilhean D, Brice A, Durr A. Huin V, et al. Among authors: gaymard b. Brain. 2022 Jun 30;145(6):2121-2132. doi: 10.1093/brain/awab449. Brain. 2022. PMID: 34927205 Free article.
Delayed Benefit From Aggressive Immunotherapy in Waxing and Waning Anti-IgLON5 Disease.
Shambrook P, Hesters A, Marois C, Zemba D, Servan J, Gaymard B, Pico F, Delorme C, Lubetzki C, Arnulf I, Psimaras D, Honnorat J, Gales A, Méneret A. Shambrook P, et al. Among authors: gaymard b. Neurol Neuroimmunol Neuroinflamm. 2021 May 13;8(4):e1009. doi: 10.1212/NXI.0000000000001009. Print 2021 Jul. Neurol Neuroimmunol Neuroinflamm. 2021. PMID: 33986128 Free PMC article. No abstract available.
Further evidence for a distinctive atypical degenerative parkinsonism in the Caribbean: A new cluster in the French West Indian Island of Martinique.
Lannuzel A, Edragas R, Lackmy A, Tressières B, Pelonde V, Kaptué MEN, Mécharles S, Demas A, François B, McGovern E, Vidailhet M, Gaymard B, Roze E. Lannuzel A, et al. Among authors: gaymard b. J Neurol Sci. 2018 May 15;388:214-219. doi: 10.1016/j.jns.2018.02.019. Epub 2018 Feb 6. J Neurol Sci. 2018. PMID: 29525296
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein.
Mariani LL, Rivaud-Péchoux S, Charles P, Ewenczyk C, Meneret A, Monga BB, Fleury MC, Hainque E, Maisonobe T, Degos B, Echaniz-Laguna A, Renaud M, Wirth T, Grabli D, Brice A, Vidailhet M, Stoppa-Lyonnet D, Dubois-d'Enghien C, Le Ber I, Koenig M, Roze E, Tranchant C, Durr A, Gaymard B, Anheim M. Mariani LL, et al. Among authors: gaymard b. Sci Rep. 2017 Nov 10;7(1):15284. doi: 10.1038/s41598-017-15127-9. Sci Rep. 2017. PMID: 29127364 Free PMC article. Clinical Trial.
111 results