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Rui Han Liu

Showing results (11-20 of 28) with videos related to

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Insights Into Imaging|April 8, 2024
Geospatial evaluation of radiologic access in RwandaRui Han Liu, Michael Lindeborg, Isaie Ncogoza, et al.
Aesthetic Plastic Surgery|August 23, 2024
A Scoping Review on Complications in Modern Hair Transplantation: More than Just Splitting HairsRui Han Liu, Lucy J Xu, Justin C McCarty, et al.
Annals of Vascular Surgery|June 11, 2018
Removal of Noninfected Arteriovenous Fistulae after Kidney Transplantation is a Safe and Beneficial Management Strategy for Unused Dialysis AccessCharles D Fraser, Joshua C Grimm, Rui Han Liu, et al.
World Journal of Clinical Cases|November 7, 2022
Child with adenylosuccinate lyase deficiency caused by a novel complex heterozygous mutation in the <i>ADSL</i> gene: A case reportXing-Chen Wang, Ting Wang, Rui-Han Liu, et al.
Facial Plastic Surgery & Aesthetic Medicine|August 8, 2020
Free Functional Gracilis Flaps for Facial Reanimation in Elderly PatientsAndrew H Lee, Rui Han Liu, Lisa E Ishii, et al.
Probiotics and Antimicrobial Proteins|September 8, 2022
Lactiplantibacillus plantarum Regulated Intestinal Microbial Community and Cytokines to Inhibit Salmonella typhimurium InfectionRui-Han Liu, An-Qi Sun, Ye Liao, et al.
Experimental and Therapeutic Medicine|April 9, 2024
Eukaryotic translation initiation factor <i>EIF4G1</i> p.Ser637Cys mutation in a family with Parkinson's disease with antecedent essential tremorRui-Han Liu, Xiang-Yu Xiao, Lei Yao, et al.
The Annals of Thoracic Surgery|January 25, 2018
Coronary Button Pseudoaneurysms After Aortic Root Replacement in a Child With Loeys-Deitz SyndromeCharles D Fraser, Xun Zhou, Rui Han Liu, et al.
JAMA Otolaryngology-- Head & Neck Surgery|January 10, 2020
Association of Hypocalcemia and Magnesium Disorders With Thyroidectomy in Commercially Insured PatientsRui Han Liu, Christopher R Razavi, Hsien-Yen Chang, et al.
World Journal of Clinical Cases|October 30, 2023
Compound heterozygous mutations in tripeptidyl peptidase 1 cause rare autosomal recessive spinocerebellar ataxia type 7: A case reportRui-Han Liu, Xin-Yu Wang, Yuan-Yuan Jia, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Insights Into Imaging|April 8, 2024
Geospatial evaluation of radiologic access in RwandaRui Han Liu, Michael Lindeborg, Isaie Ncogoza, et al.
Aesthetic Plastic Surgery|August 23, 2024
A Scoping Review on Complications in Modern Hair Transplantation: More than Just Splitting HairsRui Han Liu, Lucy J Xu, Justin C McCarty, et al.
Annals of Vascular Surgery|June 11, 2018
Removal of Noninfected Arteriovenous Fistulae after Kidney Transplantation is a Safe and Beneficial Management Strategy for Unused Dialysis AccessCharles D Fraser, Joshua C Grimm, Rui Han Liu, et al.
World Journal of Clinical Cases|November 7, 2022
Child with adenylosuccinate lyase deficiency caused by a novel complex heterozygous mutation in the <i>ADSL</i> gene: A case reportXing-Chen Wang, Ting Wang, Rui-Han Liu, et al.
Facial Plastic Surgery & Aesthetic Medicine|August 8, 2020
Free Functional Gracilis Flaps for Facial Reanimation in Elderly PatientsAndrew H Lee, Rui Han Liu, Lisa E Ishii, et al.
Probiotics and Antimicrobial Proteins|September 8, 2022
Lactiplantibacillus plantarum Regulated Intestinal Microbial Community and Cytokines to Inhibit Salmonella typhimurium InfectionRui-Han Liu, An-Qi Sun, Ye Liao, et al.
Experimental and Therapeutic Medicine|April 9, 2024
Eukaryotic translation initiation factor <i>EIF4G1</i> p.Ser637Cys mutation in a family with Parkinson's disease with antecedent essential tremorRui-Han Liu, Xiang-Yu Xiao, Lei Yao, et al.
The Annals of Thoracic Surgery|January 25, 2018
Coronary Button Pseudoaneurysms After Aortic Root Replacement in a Child With Loeys-Deitz SyndromeCharles D Fraser, Xun Zhou, Rui Han Liu, et al.
JAMA Otolaryngology-- Head & Neck Surgery|January 10, 2020
Association of Hypocalcemia and Magnesium Disorders With Thyroidectomy in Commercially Insured PatientsRui Han Liu, Christopher R Razavi, Hsien-Yen Chang, et al.
World Journal of Clinical Cases|October 30, 2023
Compound heterozygous mutations in tripeptidyl peptidase 1 cause rare autosomal recessive spinocerebellar ataxia type 7: A case reportRui-Han Liu, Xin-Yu Wang, Yuan-Yuan Jia, et al.
Pageof 3