Moore, Ursula RJacobs, MarniFernandez-Torron, RobertoJang, JijiJames, Meredith KMayhew, AnnaRufibach, LauraMittal, PlaviEagle, MichelleCnaan, AvitalCarlier, Pierre GBlamire, AndrewHilsden, HeatherLochmüller, HannsGrieben, UlrikeSpuler, SimoneTesi-Rocha, CarolinaDay, John WJones, Kristi JBharucha-Goebel, Diana XSalort-Campana, EmmanuelleHarms, MatthewPestronk, AlanKrause, SabineSchreiber-Katz, OliviaWalter, Maggie CParadas, CarmenHogrel, Jean-YvesStojkovic, TanyaTakeda, Shin'ichiMori-Yoshimura, MadokaBravver, ElenaSparks, SusanDiaz-Manera, JordiBello, LucaSemplicini, ClaudioPegoraro, ElenaMendell, Jerry RBushby, KateStraub, Volker2023-01-252023-01-252018-11Moore UR, Jacobs M, Fernandez-Torron R, Jang J, James MK, et al. Teenage exercise is associated with earlier symptom onset in dysferlinopathy: a retrospective cohort study. J Neurol Neurosurg Psychiatry. 2018 Nov;89(11):1224-1226.http://hdl.handle.net/10668/12060Dysferlinopathy, an autosomal recessive muscular dystrophy caused by DYSF mutations, demonstrates a variable phenotype and progression rate, with symptom onset ranging from first to eighth decade and some patients requiring wheelchairs for mobility within 10 years, with others remaining minimally affected.1enAttribution 4.0 Internationalhttp://creativecommons.org/licenses/by/4.0/muscular dystrophyneuromuscularDysferlinopathyAdolescent BehaviorAge of OnsetMiddle AgedMuscular Dystrophies, Limb-GirdleAdolescent BehaviorAdultAge FactorsExerciseFemaleHumansMaleRetrospective StudiesSurveys and QuestionnairesYoung Adultletter29378789open accessDistrofias muscularesEnfermedades hereditarias autosómicas recesivasGenes DYSFDebilidad muscularTrastornos neuromuscularesInicio de los síntomasProgresión de la enfermedadLimitación de la movilidad10.1136/jnnp-2017-3173291468-330XPMC6227796https://jnnp.bmj.com/content/jnnp/89/11/1224.full.pdfhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6227796/pdf