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Jiuwei Li

Showing results (41-50 of 45) with videos related to

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Orphanet Journal of Rare Diseases|January 24, 2026
Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial diseaseChaolong Xu, Hong Jin, Jiuwei Li, et al.
Molecular Genetics and Genomics : MGG|October 26, 2024
A novel m.5906G > a variant in MT-CO1 causes MELAS/Leigh overlap syndromeZhimei Liu, Yaojun Xie, Xiaoting Lou, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 16, 2021
Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center studyWeihua Zhang, Changhong Ren, Xiaohui Wang, et al.
Chemosphere|January 12, 2024
Hydrolytic degradation and biodegradation of polylactic acid electrospun fibersXiang Yun Debbie Soo, Linran Jia, Qi Feng Lim, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|August 2, 2021
HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respirationYu Sun, Xiujuan Wei, Fang Fang, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Orphanet Journal of Rare Diseases|January 24, 2026
Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial diseaseChaolong Xu, Hong Jin, Jiuwei Li, et al.
Molecular Genetics and Genomics : MGG|October 26, 2024
A novel m.5906G > a variant in MT-CO1 causes MELAS/Leigh overlap syndromeZhimei Liu, Yaojun Xie, Xiaoting Lou, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 16, 2021
Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center studyWeihua Zhang, Changhong Ren, Xiaohui Wang, et al.
Chemosphere|January 12, 2024
Hydrolytic degradation and biodegradation of polylactic acid electrospun fibersXiang Yun Debbie Soo, Linran Jia, Qi Feng Lim, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|August 2, 2021
HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respirationYu Sun, Xiujuan Wei, Fang Fang, et al.
Pageof 5