Shen XM - Search Results

1

Comparison between mono-tacrolimus and mono-glucocorticoid in the treatment of myasthenia gravis.

Fan Z, Lei L, Su S, Zhang S, Xie N, Li L, Lu Y, Di L, Wang M, Xu M, Shen XM, Da Y. Fan Z, et al. Among authors: shen xm. Ann Clin Transl Neurol. 2023 Apr;10(4):589-598. doi: 10.1002/acn3.51746. Epub 2023 Feb 20. Ann Clin Transl Neurol. 2023. PMID: 36808840 Free PMC article.

2

Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patients.

Selcen D, Milone M, Shen XM, Harper CM, Stans AA, Wieben ED, Engel AG. Selcen D, et al. Among authors: shen xm. Ann Neurol. 2008 Jul;64(1):71-87. doi: 10.1002/ana.21408. Ann Neurol. 2008. PMID: 18626973 Free PMC article.

3

Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation.

Di L, Chen H, Da Y, Wang S, Shen XM. Di L, et al. Among authors: shen xm. J Neurol. 2016 Feb;263(2):263-268. doi: 10.1007/s00415-015-7965-3. Epub 2015 Nov 14. J Neurol. 2016. PMID: 26566915

4

A unique case of dysferlinopathy with a large-segment duplication mutation who experienced rapid deterioration after small-dosage corticosteroid treatment.

Di L, Guan Y, Shen XM, Da Y. Di L, et al. Among authors: shen xm. J Neurol Sci. 2017 May 15;376:35-37. doi: 10.1016/j.jns.2017.02.059. Epub 2017 Feb 27. J Neurol Sci. 2017. PMID: 28431623 No abstract available.

5

Monoclonal gammopathy with both nemaline myopathy and amyloid myopathy.

Wang M, Lei L, Chen H, Di L, Pang M, Lu Y, Lu L, Shen XM, Da Y. Wang M, et al. Among authors: shen xm. Neuromuscul Disord. 2017 Oct;27(10):942-946. doi: 10.1016/j.nmd.2017.05.007. Epub 2017 May 11. Neuromuscul Disord. 2017. PMID: 28606401

6

Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain.

Sun Y, Chen H, Lu Y, Duo J, Lei L, OuYang Y, Hao Y, Da Y, Shen XM. Sun Y, et al. Among authors: shen xm. J Neurol. 2019 Feb;266(2):498-506. doi: 10.1007/s00415-018-9165-4. Epub 2019 Jan 2. J Neurol. 2019. PMID: 30604053

7

Presence of antibodies against low-density lipoprotein receptor-related protein 4 and impairment of neuromuscular junction in a Chinese cohort of amyotrophic lateral sclerosis.

Lei L, Shen XM, Wang SY, Lu Y, Wang SB, Chen H, Liu Z, Ouyang YS, Duo JY, Da YW, Chen ZG. Lei L, et al. Among authors: shen xm. Chin Med J (Engl). 2019 Jun 20;132(12):1487-1489. doi: 10.1097/CM9.0000000000000284. Chin Med J (Engl). 2019. PMID: 31205110 Free PMC article.

8

Slow-channel myasthenia due to novel mutation in M2 domain of AChR delta subunit.

Shen XM, Milone M, Wang HL, Banwell B, Selcen D, Sine SM, Engel AG. Shen XM, et al. Ann Clin Transl Neurol. 2019 Oct;6(10):2066-2078. doi: 10.1002/acn3.50902. Epub 2019 Sep 27. Ann Clin Transl Neurol. 2019. PMID: 31560172 Free PMC article.

9

A novel fast-channel myasthenia caused by mutation in β subunit of AChR reveals subunit-specific contribution of the intracellular M1-M2 linker to channel gating.

Shen XM, Di L, Shen S, Zhao Y, Neumeyer AM, Selcen D, Sine SM, Engel AG. Shen XM, et al. Among authors: shen s. Exp Neurol. 2020 Sep;331:113375. doi: 10.1016/j.expneurol.2020.113375. Epub 2020 Jun 3. Exp Neurol. 2020. PMID: 32504635 Free PMC article.

10

Determinants of the repetitive-CMAP occurrence and therapy efficacy in slow-channel myasthenia.

Di L, Chen H, Lu Y, Selcen D, Engel AG, Da Y, Shen XM. Di L, et al. Among authors: shen xm. Neurology. 2020 Nov 17;95(20):e2781-e2793. doi: 10.1212/WNL.0000000000010734. Epub 2020 Sep 9. Neurology. 2020. PMID: 32907971 Free PMC article.

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