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Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls.
Reimann J, Lehmann D, Hardy SA, Falkous G, Knowles CV, Jones RL, Kunz WS, Taylor RW, Kornblum C. Reimann J, et al. Among authors: jones rl. Neurol Genet. 2017 Apr 5;3(3):e147. doi: 10.1212/NXG.0000000000000147. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28396884 Free PMC article. No abstract available.
Opening One's Eyes to Mosaicism in Progressive External Ophthalmoplegia.
Sommerville EW, Jones RL, Hardy SA, Blakely EL, Pyle A, Schaefer AM, Chinnery PF, Turnbull DM, Gorman GS, Taylor RW. Sommerville EW, et al. Among authors: jones rl. Neurol Genet. 2017 Dec 15;3(6):e202. doi: 10.1212/NXG.0000000000000202. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264394 Free PMC article. No abstract available.
Advancing Systemic Therapy in Chondrosarcoma: New Horizons.
Li KHC, Gulia A, Duffaud F, Jones RL. Li KHC, et al. Among authors: jones rl. Oncol Ther. 2024 Dec 9. doi: 10.1007/s40487-024-00317-z. Online ahead of print. Oncol Ther. 2024. PMID: 39652252 Free article.
International Multicenter Retrospective Study From the Ultra-rare Sarcoma Working Group on Low-grade Fibromyxoid Sarcoma, Sclerosing Epithelioid Fibrosarcoma, and Hybrid Forms: Outcome of Primary Localized Disease.
Giani C, Salawu A, Ljevar S, Denu RA, Napolitano A, Palmerini E, Connolly EA, Ogura K, Wong DD, Scanferla R, Rosenbaum E, Bajpai J, Li ZC, Bae S, D'Ambrosio L, Bialick S, Wagner AJ, Lee ATJ, Koseła-Paterczyk H, Baldi GG, Brunello A, Lee YC, Loong HH, Boikos S, Campos F, Cicala CM, Maki RG, Hindi N, Figura C, Almohsen SS, Patel S, Jones RL, Ibrahim T, Karim R, Kawai A, Carey-Smith R, Boyle R, Taverna SM, Lazar AJ, Demicco EG, Bovee JVMG, Dei Tos AP, Fletcher C, Baumhoer D, Sbaraglia M, Schaefer IM, Miceli R, Gronchi A, Stacchiotti S. Giani C, et al. Among authors: jones rl. Am J Surg Pathol. 2025 Jan 1;49(1):27-34. doi: 10.1097/PAS.0000000000002330. Epub 2024 Oct 28. Am J Surg Pathol. 2025. PMID: 39466087 Free PMC article.
1,375 results