Yu M - Search Results

1

Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa.

Li Z, Li Y, Chu X, Du K, Tang Y, Xie Z, Yu M, Deng J, Lv H, Zhang W, Wang Z, Meng L, Yuan Y. Li Z, et al. Among authors: yu m. Neuropathology. 2024 Apr;44(2):87-95. doi: 10.1111/neup.12936. Epub 2023 Jul 19. Neuropathology. 2024. PMID: 37469134

2

Clinical and Brain Magnetic Resonance Imaging Features in a Cohort of Chinese Patients with Kearns-Sayre Syndrome.

Yu M, Zhang Z, Wang QQ, Liu J, Zuo YH, Yu L, Xiao JX, Zhang W, Yuan Y, Wang ZX. Yu M, et al. Among authors: yu l. Chin Med J (Engl). 2016 Jun 20;129(12):1419-24. doi: 10.4103/0366-6999.183417. Chin Med J (Engl). 2016. PMID: 27270536 Free PMC article.

3

Dysferlin Gene Mutation Spectrum in a Large Cohort of Chinese Patients with Dysferlinopathy.

Jin SQ, Yu M, Zhang W, Lyu H, Yuan Y, Wang ZX. Jin SQ, et al. Among authors: yu m. Chin Med J (Engl). 2016 Oct 5;129(19):2287-93. doi: 10.4103/0366-6999.190671. Chin Med J (Engl). 2016. PMID: 27647186 Free PMC article.

4

Diagnosis and Management of Kearns-Sayre Syndrome Rely on Comprehensive Clinical Evaluation.

Yu M, Yu L, Wang ZX. Yu M, et al. Among authors: yu l. Chin Med J (Engl). 2016 Oct 20;129(20):2519-2520. doi: 10.4103/0366-6999.191855. Chin Med J (Engl). 2016. PMID: 27748354 Free PMC article. No abstract available.

5

Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing.

Yu M, Zheng Y, Jin S, Gang Q, Wang Q, Yu P, Lv H, Zhang W, Yuan Y, Wang Z. Yu M, et al. Among authors: yu p. PLoS One. 2017 Apr 12;12(4):e0175343. doi: 10.1371/journal.pone.0175343. eCollection 2017. PLoS One. 2017. PMID: 28403181 Free PMC article.

6

Study of Enhanced Depth Imaging Optical Coherence Tomography in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.

Fang XJ, Yu M, Wu Y, Zhang ZH, Wang WW, Wang ZX, Yuan Y. Fang XJ, et al. Among authors: yu m. Chin Med J (Engl). 2017 May 5;130(9):1042-1048. doi: 10.4103/0366-6999.204935. Chin Med J (Engl). 2017. PMID: 28469098 Free PMC article.

7

AARS2 Compound Heterozygous Variants in a Case of Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia.

Wang D, Yu M, Zhang W, Wang Z, Yuan Y. Wang D, et al. Among authors: yu m. J Neuropathol Exp Neurol. 2018 Nov 1;77(11):997-1000. doi: 10.1093/jnen/nly087. J Neuropathol Exp Neurol. 2018. PMID: 30272204

8

Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients.

Xie Z, Hou Y, Yu M, Liu Y, Fan Y, Zhang W, Wang Z, Xiong H, Yuan Y. Xie Z, et al. Among authors: yu m. Orphanet J Rare Dis. 2019 Feb 14;14(1):43. doi: 10.1186/s13023-019-1021-9. Orphanet J Rare Dis. 2019. PMID: 30764848 Free PMC article.

9

Novel TTN mutations and muscle imaging characteristics in congenital titinopathy.

Yu M, Zhu Y, Xie Z, Zheng Y, Xiao J, Zhang W, Nishino I, Yuan Y, Wang Z. Yu M, et al. Ann Clin Transl Neurol. 2019 Jul;6(7):1311-1318. doi: 10.1002/acn3.50831. Epub 2019 Jul 1. Ann Clin Transl Neurol. 2019. PMID: 31353864 Free PMC article.

10

Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex.

Xie Z, Xie Z, Yu M, Zheng Y, Sun C, Liu Y, Ling C, Zhu Y, Zhang W, Xiao J, Wang Z, Yuan Y. Xie Z, et al. Among authors: yu m. Orphanet J Rare Dis. 2019 Nov 12;14(1):250. doi: 10.1186/s13023-019-1242-y. Orphanet J Rare Dis. 2019. PMID: 31747956 Free PMC article.

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