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226th ENMC International Workshop:: Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20-22 January 2017, Heemskerk, The Netherlands.
Aartsma-Rus A, Ferlini A, McNally EM, Spitali P, Sweeney HL; workshop participants. Aartsma-Rus A, et al. Among authors: sweeney hl. Neuromuscul Disord. 2018 Jan;28(1):77-86. doi: 10.1016/j.nmd.2017.10.002. Epub 2017 Oct 26. Neuromuscul Disord. 2018. PMID: 29203356 Free PMC article. No abstract available.
Muscle degeneration without mechanical injury in sarcoglycan deficiency.
Hack AA, Cordier L, Shoturma DI, Lam MY, Sweeney HL, McNally EM. Hack AA, et al. Among authors: sweeney hl. Proc Natl Acad Sci U S A. 1999 Sep 14;96(19):10723-8. doi: 10.1073/pnas.96.19.10723. Proc Natl Acad Sci U S A. 1999. PMID: 10485893 Free PMC article.
MRI/MRS evaluation of a female carrier of Duchenne muscular dystrophy.
Forbes SC, Lott DJ, Finkel RS, Senesac C, Byrne BJ, Sweeney HL, Walter GA, Vandenborne K. Forbes SC, et al. Among authors: sweeney hl. Neuromuscul Disord. 2012 Oct 1;22 Suppl 2(Suppl 2):S111-21. doi: 10.1016/j.nmd.2012.05.013. Neuromuscul Disord. 2012. PMID: 22980762 Free PMC article.
Longitudinal measurements of MRI-T2 in boys with Duchenne muscular dystrophy: effects of age and disease progression.
Willcocks RJ, Arpan IA, Forbes SC, Lott DJ, Senesac CR, Senesac E, Deol J, Triplett WT, Baligand C, Daniels MJ, Sweeney HL, Walter GA, Vandenborne K. Willcocks RJ, et al. Among authors: sweeney hl. Neuromuscul Disord. 2014 May;24(5):393-401. doi: 10.1016/j.nmd.2013.12.012. Epub 2014 Jan 11. Neuromuscul Disord. 2014. PMID: 24491484 Free PMC article.
Skeletal muscle magnetic resonance biomarkers correlate with function and sentinel events in Duchenne muscular dystrophy.
Barnard AM, Willcocks RJ, Finanger EL, Daniels MJ, Triplett WT, Rooney WD, Lott DJ, Forbes SC, Wang DJ, Senesac CR, Harrington AT, Finkel RS, Russman BS, Byrne BJ, Tennekoon GI, Walter GA, Sweeney HL, Vandenborne K. Barnard AM, et al. Among authors: sweeney hl. PLoS One. 2018 Mar 19;13(3):e0194283. doi: 10.1371/journal.pone.0194283. eCollection 2018. PLoS One. 2018. PMID: 29554116 Free PMC article.
Modeling disease trajectory in Duchenne muscular dystrophy.
Rooney WD, Berlow YA, Triplett WT, Forbes SC, Willcocks RJ, Wang DJ, Arpan I, Arora H, Senesac C, Lott DJ, Tennekoon G, Finkel R, Russman BS, Finanger EL, Chakraborty S, O'Brien E, Moloney B, Barnard A, Sweeney HL, Daniels MJ, Walter GA, Vandenborne K. Rooney WD, et al. Among authors: sweeney hl. Neurology. 2020 Apr 14;94(15):e1622-e1633. doi: 10.1212/WNL.0000000000009244. Epub 2020 Mar 17. Neurology. 2020. PMID: 32184340 Free PMC article.
Disease-modifying effects of edasalonexent, an NF-κB inhibitor, in young boys with Duchenne muscular dystrophy: Results of the MoveDMD phase 2 and open label extension trial.
Finkel RS, Finanger E, Vandenborne K, Sweeney HL, Tennekoon G, Shieh PB, Willcocks R, Walter G, Rooney WD, Forbes SC, Triplett WT, Yum SW, Mancini M, MacDougall J, Fretzen A, Bista P, Nichols A, Donovan JM. Finkel RS, et al. Among authors: sweeney hl. Neuromuscul Disord. 2021 May;31(5):385-396. doi: 10.1016/j.nmd.2021.02.001. Epub 2021 Feb 4. Neuromuscul Disord. 2021. PMID: 33678513 Free article. Clinical Trial.
281 results