M. Ma

发表

Lower limb muscle magnetic resonance imaging in Chinese patients with myotonic dystrophy type 1

Jiewen Zhang, Jia Song, Gang Li, 2020, Neurological research.

Reduced cerebral blood flow in genetic prion disease with PRNP D178N–129M mutation: An arterial spin labeling MRI study

M. Guan, Jiewen Zhang, Shuai Chen, 2015, Journal of Clinical Neuroscience.

Clinical and Genetic Features of Chinese Patients With NIPA1-Related Hereditary Spastic Paraplegia Type 6

Jiewen Zhang, Gang Li, Jun Fu, 2022, Frontiers in Genetics.

Novel mutations in DPM3 cause dystroglycanopathy with central nervous system involvement

Jiewen Zhang, Jia Song, Gang Li, 2019, Clinical genetics.

Heterozygous Seryl‐tRNA Synthetase 1 Variants Cause Charcot–Marie–Tooth Disease

M. Kennerson, Jin He, Jing Zhang, 2022, Annals of neurology.

Spreading of TDP-43 pathology via pyramidal tract induces ALS-like phenotypes in TDP-43 transgenic mice

Xuebing Ding, Xue-Jing Wang, Jia Song, 2021, Acta Neuropathologica Communications.

Association between pretreatment lymphocyte count and efficacy of immune-enhancing therapy in acute necrotising pancreatitis: a post-hoc analysis of the multicentre, randomised, placebo-controlled TRACE trial

Zhenping, Tao Chen, Gang Li, 2023, EClinicalMedicine.

BAG3 p.Pro209Ser mutation identified in a Chinese family with Charcot–Marie–Tooth disease

Jiewen Zhang, Jia Song, Gang Li, 2019, Journal of Neurology.

Effects of transcranial magnetic stimulation on the cognitive ability of patients with cognitive impairment after cerebral venous thrombosis

Changshui Xu, Jia Song, Gang Li, 2017 .

High-risk screening for late-onset Pompe disease in China: An expanded multicenter study.

Lijun Du, J. Xi, Zhe Zhao, 2024, Journal of inherited metabolic disease.