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

Year Number of Results
2004 1
2006 1
2010 2
2012 2
2015 2
2016 1
2017 2
2018 1
2019 1
2020 7
2021 5
2022 9
2023 4
2024 1

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33 results

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Page 1
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia.
Pellerin D, Danzi MC, Wilke C, Renaud M, Fazal S, Dicaire MJ, Scriba CK, Ashton C, Yanick C, Beijer D, Rebelo A, Rocca C, Jaunmuktane Z, Sonnen JA, Larivière R, Genís D, Molina Porcel L, Choquet K, Sakalla R, Provost S, Robertson R, Allard-Chamard X, Tétreault M, Reiling SJ, Nagy S, Nishadham V, Purushottam M, Vengalil S, Bardhan M, Nalini A, Chen Z, Mathieu J, Massie R, Chalk CH, Lafontaine AL, Evoy F, Rioux MF, Ragoussis J, Boycott KM, Dubé MP, Duquette A, Houlden H, Ravenscroft G, Laing NG, Lamont PJ, Saporta MA, Schüle R, Schöls L, La Piana R, Synofzik M, Zuchner S, Brais B. Pellerin D, et al. Among authors: massie r. N Engl J Med. 2023 Jan 12;388(2):128-141. doi: 10.1056/NEJMoa2207406. Epub 2022 Dec 14. N Engl J Med. 2023. PMID: 36516086 Free PMC article.
Autoimmune peripheral neuropathies.
Bourque PR, Chardon JW, Massie R. Bourque PR, et al. Among authors: massie r. Clin Chim Acta. 2015 Sep 20;449:37-42. doi: 10.1016/j.cca.2015.02.039. Epub 2015 Mar 4. Clin Chim Acta. 2015. PMID: 25748038 Review.
Canadian Guidelines for Hereditary Transthyretin Amyloidosis Polyneuropathy Management.
Alcantara M, Mezei MM, Baker SK, Breiner A, Dhawan P, Fiander A, Fine NM, Hahn C, Katzberg HD, Khayambashi S, Massie R, Matte G, Putko B, Siddiqi Z, Delgado D, Bril V. Alcantara M, et al. Among authors: massie r. Can J Neurol Sci. 2022 Jan;49(1):7-18. doi: 10.1017/cjn.2021.34. Epub 2021 Feb 26. Can J Neurol Sci. 2022. PMID: 33631091 Review.
Diabetic Cranio-Cervico-Radiculoplexus Neuropathy.
Gupta G, Massie R, Doherty TJ, Bourque PR, Radhakrishna M, Finlayson RJ, Besemann M, Simantirakis E, Dyck PJB. Gupta G, et al. Among authors: massie r. PM R. 2015 Nov;7(11):1189-1193. doi: 10.1016/j.pmrj.2015.05.003. Epub 2015 May 12. PM R. 2015. PMID: 25978945
Scapuloperoneal syndrome with mitochondrial DNA deletion.
Pichette É, O'Ferrall E, Karamchandani J, Savarese M, Udd B, Massie R. Pichette É, et al. Among authors: massie r. J Neurol Sci. 2022 Mar 15;434:120164. doi: 10.1016/j.jns.2022.120164. Epub 2022 Jan 29. J Neurol Sci. 2022. PMID: 35121208 No abstract available.
Teaching NeuroImages: Sneddon syndrome.
Almutlaq A, Alshurem M, Levesque-Roy M, Massie R. Almutlaq A, et al. Among authors: massie r. Neurology. 2019 Sep 17;93(12):e1227-e1228. doi: 10.1212/WNL.0000000000008137. Neurology. 2019. PMID: 31527109 No abstract available.
Polymerase gamma 1 mutations: clinical correlations.
Milone M, Massie R. Milone M, et al. Among authors: massie r. Neurologist. 2010 Mar;16(2):84-91. doi: 10.1097/NRL.0b013e3181c78a89. Neurologist. 2010. PMID: 20220442 Review.
Autoantibody profiles delineate distinct subsets of scleromyositis.
Leclair V, D'Aoust J, Gyger G, Landon-Cardinal O, Meyer A, O'Ferrall E, Karamchandani J, Massie R, Ellezam B, Satoh M, Troyanov Y, Fritzler MJ, Hudson M; Canadian Inflammatory Myopathy Study Group. Leclair V, et al. Among authors: massie r. Rheumatology (Oxford). 2022 Mar 2;61(3):1148-1157. doi: 10.1093/rheumatology/keab492. Rheumatology (Oxford). 2022. PMID: 34146090
33 results