Yuwei Da

The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4

Jiaxi Yu, Jingli Shan, Meng Yu et al. · The American Journal of Human Genetics · 2022 · 77 citations · Full text

Cgg Repeat Expansion, Autoimmune Disease, Genetic Disorder +4

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

Yanan Sun, Yan Lü, Jianying Duo et al. · Journal of Neurology · 2019 · 53 citations

Distal Muscle Weakness, Rare Diseases, Chinese Family +9

Brain MRI features and scoring of leukodystrophy in adult-onset Krabbe disease

Louis Cousyn, Bruno Law-Ye, Nadya Pyatigorskaya et al. · Neurology · 2019 · 36 citations

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

Di Li, Hai Chen, Yuwei Da et al. · Journal of Neurology · 2015 · 28 citations

Vapb-p56s Mutation, Chinese Family, Neurobiology Of Disease +10

Favorable Effects of Tacrolimus Monotherapy on Myasthenia Gravis Patients

Zhirong Fan, Zunbo Li, Faxiu Shen et al. · Frontiers in Neurology · 2020 · 26 citations · Full text