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Autosomal dominant distal myopathy due to a novel ACTA1 mutation.
Liewluck T, Sorenson EJ, Walkiewicz MA, Rumilla KM, Milone M. Liewluck T, et al. Among authors: sorenson ej. Neuromuscul Disord. 2017 Aug;27(8):742-746. doi: 10.1016/j.nmd.2017.05.003. Epub 2017 May 5. Neuromuscul Disord. 2017. PMID: 28606400
Triple Furrowed Atrophic Tongue of Myasthenia Gravis.
Young NP, Sorenson EJ, Milone M, Harper CM. Young NP, et al. Among authors: sorenson ej. J Clin Neuromuscul Dis. 2017 Sep;19(1):47-48. doi: 10.1097/CND.0000000000000171. J Clin Neuromuscul Dis. 2017. PMID: 28827490
Myotonia associated with caveolin-3 mutation.
Milone M, McEvoy KM, Sorenson EJ, Daube JR. Milone M, et al. Among authors: sorenson ej. Muscle Nerve. 2012 Jun;45(6):897-900. doi: 10.1002/mus.23270. Muscle Nerve. 2012. PMID: 22581547
Clinical spectrum of valosin containing protein (VCP)-opathy.
Kazamel M, Sorenson EJ, McEvoy KM, Jones LK Jr, Leep-Hunderfund AN, Mauermann ML, Milone M. Kazamel M, et al. Among authors: sorenson ej. Muscle Nerve. 2016 Jun;54(1):94-9. doi: 10.1002/mus.24980. Epub 2015 Dec 29. Muscle Nerve. 2016. PMID: 26574898
131 results