Yue D - Search Results

1

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. 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

2

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: yue d. 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

3

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: yue d. 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

4

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: yue d. Muscle Nerve. 2016 Dec;54(6):1059-1063. doi: 10.1002/mus.25169. Epub 2016 Oct 11. Muscle Nerve. 2016. PMID: 27145478

5

Novel mutations in the C-terminal region of GMPPB causing limb-girdle muscular dystrophy overlapping with congenital myasthenic syndrome.

Luo S, Cai S, Maxwell S, Yue D, Zhu W, Qiao K, Zhu Z, Zhou L, Xi J, Lu J, Beeson D, Zhao C. Luo S, et al. Among authors: yue d. Neuromuscul Disord. 2017 Jun;27(6):557-564. doi: 10.1016/j.nmd.2017.03.004. Epub 2017 Mar 10. Neuromuscul Disord. 2017. PMID: 28433477

6

Exertional myalgia, contractures and annular erythema in a patient with muscle lactate dehydrogenase (LDH) deficiency.

Yue D, Zhu W, Zhao C. Yue D, et al. Neuromuscul Disord. 2018 Jan;28(1):59. doi: 10.1016/j.nmd.2017.09.013. Epub 2017 Oct 5. Neuromuscul Disord. 2018. PMID: 29198466 No abstract available.

7

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: yue d. Muscle Nerve. 2018 Oct;58(4):536-541. doi: 10.1002/mus.26169. Epub 2018 Sep 3. Muscle Nerve. 2018. PMID: 29797799

8

Statin-naïve anti-HMGCR antibody-mediated necrotizing myopathy in China.

Jiao Y, Cai S, Lin J, Zhu W, Xi J, Li J, Yue D, Zhang T, Qiao K, Wang Y, Zhao C, Lu J. Jiao Y, et al. Among authors: yue d. J Clin Neurosci. 2018 Nov;57:13-19. doi: 10.1016/j.jocn.2018.08.010. Epub 2018 Sep 8. J Clin Neurosci. 2018. PMID: 30205933

9

GNE myopathy in Chinese population: hotspot and novel mutations.

Chen Y, Xi J, Zhu W, Lin J, Luo S, Yue D, Cai S, Sun C, Zhao C, Mitsuhashi S, Nishino I, Xu M, Lu J. Chen Y, et al. Among authors: yue d. J Hum Genet. 2019 Jan;64(1):11-16. doi: 10.1038/s10038-018-0525-9. Epub 2018 Nov 2. J Hum Genet. 2019. PMID: 30390020

10

Correction: GNE myopathy in Chinese population: hotspot and novel mutations.

Chen Y, Xi J, Zhu W, Lin J, Luo S, Yue D, Cai S, Sun C, Zhao C, Mitsuhashi S, Nishino I, Xu M, Lu J. Chen Y, et al. Among authors: yue d. J Hum Genet. 2019 Mar;64(3):269. doi: 10.1038/s10038-018-0547-3. J Hum Genet. 2019. PMID: 30585253

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