Lu J - Search Results

1

Fatty infiltration evaluation and selective pattern characterization of lower limbs in limb-girdle muscular dystrophy type 2A by muscle magnetic resonance imaging.

Feng X, Luo S, Li J, Yue D, Xi J, Zhu W, Gao X, Guan X, Lu J, Liang Z, Zhao C. Feng X, et al. Among authors: lu j. Muscle Nerve. 2018 Oct;58(4):536-541. doi: 10.1002/mus.26169. Epub 2018 Sep 3. Muscle Nerve. 2018. PMID: 29797799

2

Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Xi J, Wen B, Lin J, Zhu W, Luo S, Zhao C, Li D, Lin P, Lu J, Yan C. Xi J, et al. Among authors: lu j. J Inherit Metab Dis. 2014 May;37(3):399-404. doi: 10.1007/s10545-013-9671-6. Epub 2013 Dec 20. J Inherit Metab Dis. 2014. PMID: 24357026

3

Double filtration plasmapheresis benefits myasthenia gravis patients through an immunomodulatory action.

Zhang L, Liu J, Wang H, Zhao C, Lu J, Xue J, Gu Y, Hao C, Lin S, Lv C. Zhang L, et al. Among authors: lu j. J Clin Neurosci. 2014 Sep;21(9):1570-4. doi: 10.1016/j.jocn.2013.11.046. Epub 2014 May 9. J Clin Neurosci. 2014. PMID: 24814857 Clinical Trial.

4

Multiple deep white matter lesions mimic multiple sclerosis as an unusual complication of left atrial myxoma.

Quan C, ZhangBao J, Luo S, Fang K, Xi J, Du Z, Zhao C, Lu J. Quan C, et al. Among authors: lu j. Mult Scler. 2015 Jan;21(1):108-10. doi: 10.1177/1352458514535677. Epub 2014 May 22. Mult Scler. 2015. PMID: 24852922

5

Giant cell polymyositis associated with myasthenia gravis and thymoma.

Lin J, Lu J, Zhao C, Qiao K, Zhu W, Yue D, Luo S, Wang Y, Fang W, Lu J. Lin J, et al. Among authors: lu j. J Clin Neurosci. 2014 Dec;21(12):2252-4. doi: 10.1016/j.jocn.2014.04.027. Epub 2014 Aug 2. J Clin Neurosci. 2014. PMID: 25096712

6

New disease allele and de novo mutation indicate mutational vulnerability of titin exon 343 in hereditary myopathy with early respiratory failure.

Yue D, Gao M, Zhu W, Luo S, Xi J, Wang B, Li Y, Cai S, Li J, Wang Y, Lu J, Zhao C. Yue D, et al. Among authors: lu j. Neuromuscul Disord. 2015 Feb;25(2):172-6. doi: 10.1016/j.nmd.2014.11.005. Epub 2014 Nov 18. Neuromuscul Disord. 2015. PMID: 25500009

7

Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathy.

Xi J, Blandin G, Lu J, Luo S, Zhu W, Béroud C, Pécheux C, Labelle V, Lévy N, Urtizberea JA, Zhao C, Krahn M. Xi J, et al. Among authors: lu j. Neurol India. 2014 Nov-Dec;62(6):635-9. doi: 10.4103/0028-3886.149386. Neurol India. 2014. PMID: 25591676 Free article.

8

The immune balance between memory and regulatory B cells in NMO and the changes of the balance after methylprednisolone or rituximab therapy.

Quan C, ZhangBao J, Lu J, Zhao C, Cai T, Wang B, Yu H, Qiao J, Lu C. Quan C, et al. Among authors: lu j, lu c. J Neuroimmunol. 2015 May 15;282:45-53. doi: 10.1016/j.jneuroim.2015.03.016. Epub 2015 Mar 21. J Neuroimmunol. 2015. PMID: 25903728

9

Muscle pathology and whole-body MRI in a polyglucosan myopathy associated with a novel glycogenin-1 mutation.

Luo S, Zhu W, Yue D, Lin J, Wang Y, Zhu Z, Qiu W, Lu J, Hedberg-Oldfors C, Oldfors A, Zhao C. Luo S, et al. Among authors: lu j. Neuromuscul Disord. 2015 Oct;25(10):780-5. doi: 10.1016/j.nmd.2015.07.007. Epub 2015 Jul 15. Neuromuscul Disord. 2015. PMID: 26255073

10

Clinical features and long exercise test in Chinese patients with Andersen-Tawil syndrome.

Song J, Luo S, Cheng X, Yue D, Zhu W, Lin J, Huang J, Lu J, Zhao C, Qiao K. Song J, et al. Among authors: lu j. Muscle Nerve. 2016 Dec;54(6):1059-1063. doi: 10.1002/mus.25169. Epub 2016 Oct 11. Muscle Nerve. 2016. PMID: 27145478

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