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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Pu Miao

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Neurogenetics|March 31, 2020

Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1Jianda Wang, Yanqi Hou, Lina Qi, et al.

Chinese Medical Journal|June 18, 2019

Diagnosis of intellectual disability/global developmental delay via genetic analysis in a central region of ChinaLi-Hong Liao, Chen Chen, Jing Peng, et al.

Epilepsia Open|October 24, 2025

Differential glymphatic dysfunction and memory correlation in temporal lobe epilepsy subtypesRuotong Chen, Hong Li, Pu Miao, et al.

Clinical and Translational Gastroenterology|May 26, 2023

Efficacy and Safety of Keverprazan Compared With Lansoprazole in the Treatment of Duodenal Ulcer: A Phase III, Randomized, Double-Blind, Multicenter TrialNian-di Tan, Xin-Pu Miao, Ai-Jun Liao, et al.

Pageof 5

Search research articles

Showing results (41-50 of 44) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 44 results.

Neurogenetics|March 31, 2020

Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1Jianda Wang, Yanqi Hou, Lina Qi, et al.

Chinese Medical Journal|June 18, 2019

Diagnosis of intellectual disability/global developmental delay via genetic analysis in a central region of ChinaLi-Hong Liao, Chen Chen, Jing Peng, et al.

Epilepsia Open|October 24, 2025

Differential glymphatic dysfunction and memory correlation in temporal lobe epilepsy subtypesRuotong Chen, Hong Li, Pu Miao, et al.

Clinical and Translational Gastroenterology|May 26, 2023

Efficacy and Safety of Keverprazan Compared With Lansoprazole in the Treatment of Duodenal Ulcer: A Phase III, Randomized, Double-Blind, Multicenter TrialNian-di Tan, Xin-Pu Miao, Ai-Jun Liao, et al.

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