Search research articles
Contact Us
Filters
Showing results (91-100 of 102) with videos related to
Page
of 11
Sort By:
Frontiers in Genetics
|
March 4, 2022
The Follow-Up of Chinese Patients in cblC Type Methylmalonic Acidemia Identified Through Expanded Newborn Screening
Shiying Ling, Shengnan Wu, Ruixue Shuai, et al.
Journal of Clinical Apheresis
|
August 14, 2014
Early plasma exchange for treating ricin toxicity in children after castor bean ingestion
Cheng-feng Wang, Xiao-jing Nie, Guang-ming Chen, et al.
Journal of Medical Genetics
|
June 14, 2023
Evaluation of the clinical, biochemical, genotype and prognosis of <i>mut</i>-type methylmalonic acidemia in 365 Chinese cases
Lili Liang, Shiying Ling, Yue Yu, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology
|
June 27, 2025
Total glucosides of paeony ameliorates lupus nephritis by suppressing ZBP1-mediated PANoptosis in podocytes
Yi Wang, Qian-Qian He, Yan-Ting Zhu, et al.
Molecular Genetics & Genomic Medicine
|
October 20, 2021
Different mutations in the MMUT gene are associated with the effect of vitamin B12 in a cohort of 266 Chinese patients with mut-type methylmalonic acidemia: A retrospective study
Yue Yu, Ruixue Shuai, Lili Liang, et al.
Orphanet Journal of Rare Diseases
|
January 8, 2021
A rare mutation c.1663G > A (p.A555T) in the MMUT gene associated with mild clinical and biochemical phenotypes of methylmalonic acidemia in 30 Chinese patients
Lili Liang, Ruixue Shuai, Yue Yu, et al.
Brain Imaging and Behavior
|
July 25, 2020
Altered structural and functional connectivity in CSF1R-related leukoencephalopathy
Fei-Xia Zhan, Ze-Yu Zhu, Qing Liu, et al.
Eclinicalmedicine
|
October 27, 2025
Deep learning algorithms for identifying developmental dysplasia of the hip based on sonographic images: a retrospective, prospective, multicenter study in China
Na Xu, Tong Han, Bingxuan Huang, et al.
Translational Neurodegeneration
|
December 13, 2019
Clinicopathologic characterization and abnormal autophagy of <i>CSF1R</i>-related leukoencephalopathy
Wo-Tu Tian, Fei-Xia Zhan, Qing Liu, et al.
World Journal of Pediatrics : WJP
|
December 9, 2023
Variable phenotypes and outcomes associated with the MMACHC c.482G > A mutation: follow-up in a large CblC disease cohort
Sheng-Nan Wu, Hui-Shu E, Yue Yu, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 102) with videos related to
Sort By:
Page
of 11
Frontiers in Genetics
|
March 4, 2022
The Follow-Up of Chinese Patients in cblC Type Methylmalonic Acidemia Identified Through Expanded Newborn Screening
Shiying Ling, Shengnan Wu, Ruixue Shuai, et al.
Journal of Clinical Apheresis
|
August 14, 2014
Early plasma exchange for treating ricin toxicity in children after castor bean ingestion
Cheng-feng Wang, Xiao-jing Nie, Guang-ming Chen, et al.
Journal of Medical Genetics
|
June 14, 2023
Evaluation of the clinical, biochemical, genotype and prognosis of <i>mut</i>-type methylmalonic acidemia in 365 Chinese cases
Lili Liang, Shiying Ling, Yue Yu, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology
|
June 27, 2025
Total glucosides of paeony ameliorates lupus nephritis by suppressing ZBP1-mediated PANoptosis in podocytes
Yi Wang, Qian-Qian He, Yan-Ting Zhu, et al.
Molecular Genetics & Genomic Medicine
|
October 20, 2021
Different mutations in the MMUT gene are associated with the effect of vitamin B12 in a cohort of 266 Chinese patients with mut-type methylmalonic acidemia: A retrospective study
Yue Yu, Ruixue Shuai, Lili Liang, et al.
Orphanet Journal of Rare Diseases
|
January 8, 2021
A rare mutation c.1663G > A (p.A555T) in the MMUT gene associated with mild clinical and biochemical phenotypes of methylmalonic acidemia in 30 Chinese patients
Lili Liang, Ruixue Shuai, Yue Yu, et al.
Brain Imaging and Behavior
|
July 25, 2020
Altered structural and functional connectivity in CSF1R-related leukoencephalopathy
Fei-Xia Zhan, Ze-Yu Zhu, Qing Liu, et al.
Eclinicalmedicine
|
October 27, 2025
Deep learning algorithms for identifying developmental dysplasia of the hip based on sonographic images: a retrospective, prospective, multicenter study in China
Na Xu, Tong Han, Bingxuan Huang, et al.
Translational Neurodegeneration
|
December 13, 2019
Clinicopathologic characterization and abnormal autophagy of <i>CSF1R</i>-related leukoencephalopathy
Wo-Tu Tian, Fei-Xia Zhan, Qing Liu, et al.
World Journal of Pediatrics : WJP
|
December 9, 2023
Variable phenotypes and outcomes associated with the MMACHC c.482G > A mutation: follow-up in a large CblC disease cohort
Sheng-Nan Wu, Hui-Shu E, Yue Yu, et al.
Page
of 11