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Xiaoliu Shi

Showing results (11-20 of 49) with videos related to

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Frontiers in Medicine|December 25, 2018
Next-Generation Sequencing in Early Diagnosis of Dent Disease 1: Two Case ReportsMin Wen, Tian Shen, Ying Wang, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|June 29, 2023
Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosisLihong Bai, Liping Zheng, Binyuan Li, et al.
Molecular Medicine Reports|November 9, 2017
Genetic diagnosis and pathogenic analysis of an atypical hereditary spherocytosis combined with UGT1A1 partial deficiency: A case reportYan Yi, Xiqiang Dang, Yonggui Li, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|July 19, 2018
Serum level of brain-derived neurotrophic factor in Parkinson's disease: a meta-analysisLina Jiang, Hainan Zhang, Chunyu Wang, et al.
Revista Espanola De Enfermedades Digestivas|November 20, 2020
A novel large deletion in the APC gene associated with Gardner syndrome in a Chinese familyJunfeng Zhou, Chengbo Liang, Duxin Qing, et al.
BMC Nursing|August 22, 2022
Factors associated with instrumental support in transitional care among older people with chronic disease: a cross-sectional studyMin Cui, Jianing Hua, Xiaoliu Shi, et al.
United European Gastroenterology Journal|August 22, 2024
Immune profiling of premalignant lesions in patients with Peutz-Jeghers syndromeZhongyue Liu, Boda Wu, Xiaoliu Shi, et al.
Molecular Genetics & Genomic Medicine|July 29, 2021
Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identifiedZhongyan Xiao, Yuan Yang, Hui Huang, et al.
BMC Neurology|May 3, 2022
Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case reportJia Fang, Hui Huang, Qiang Lei, et al.
Digestive Diseases and Sciences|October 1, 2020
Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 GeneHui Huang, Xuehong Wang, Dalian Ou, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Frontiers in Medicine|December 25, 2018
Next-Generation Sequencing in Early Diagnosis of Dent Disease 1: Two Case ReportsMin Wen, Tian Shen, Ying Wang, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|June 29, 2023
Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosisLihong Bai, Liping Zheng, Binyuan Li, et al.
Molecular Medicine Reports|November 9, 2017
Genetic diagnosis and pathogenic analysis of an atypical hereditary spherocytosis combined with UGT1A1 partial deficiency: A case reportYan Yi, Xiqiang Dang, Yonggui Li, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|July 19, 2018
Serum level of brain-derived neurotrophic factor in Parkinson's disease: a meta-analysisLina Jiang, Hainan Zhang, Chunyu Wang, et al.
Revista Espanola De Enfermedades Digestivas|November 20, 2020
A novel large deletion in the APC gene associated with Gardner syndrome in a Chinese familyJunfeng Zhou, Chengbo Liang, Duxin Qing, et al.
BMC Nursing|August 22, 2022
Factors associated with instrumental support in transitional care among older people with chronic disease: a cross-sectional studyMin Cui, Jianing Hua, Xiaoliu Shi, et al.
United European Gastroenterology Journal|August 22, 2024
Immune profiling of premalignant lesions in patients with Peutz-Jeghers syndromeZhongyue Liu, Boda Wu, Xiaoliu Shi, et al.
Molecular Genetics & Genomic Medicine|July 29, 2021
Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identifiedZhongyan Xiao, Yuan Yang, Hui Huang, et al.
BMC Neurology|May 3, 2022
Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case reportJia Fang, Hui Huang, Qiang Lei, et al.
Digestive Diseases and Sciences|October 1, 2020
Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 GeneHui Huang, Xuehong Wang, Dalian Ou, et al.
Pageof 5