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Guorui Hu

Showing results (1-10 of 30) with videos related to

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Translational Pediatrics|November 11, 2024
Significance of binocular fusion in enhancing visual acuity during amblyopia treatmentZongyue Lv, Zhengyang Tao, Guorui Hu, et al.
BMC Pediatrics|October 17, 2014
Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysisBixia Zheng, Guorui Hu, Jin Yu, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|April 13, 2022
Machine Learning-Based Perihematomal Tissue Features to Predict Clinical Outcome after Spontaneous Intracerebral HemorrhageXin Qi, Guorui Hu, Haiyan Sun, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 25, 2022
[Genetic analysis of PYGL gene variants for a child with Glycogen storage disease VI]Yucan Zheng, Guiping Kong, Guorui Hu, et al.
Gene|March 1, 2026
A novel variant in ARID2 causes Coffin-Siris syndrome 6 with liver cirrhosisXueying Qian, Yvcan Zheng, Liqian Zhao, et al.
Molecular Medicine Reports|June 28, 2014
Diagnosis of ABCB11 gene mutations in children with intrahepatic cholestasis using high resolution melting analysis and direct sequencingGuorui Hu, Ping He, Zhifeng Liu, et al.
Journal of Colloid and Interface Science|December 17, 2025
Catalytic vs. thermal Si - H crosslinking polydimethylsiloxane (PDMS) elastomers: Network heterogeneity drives interfacial performanceZiheng Chen, Yongjie Gao, Guorui Hu, et al.
Photodiagnosis and Photodynamic Therapy|May 29, 2026
Sleep Quality, Sleep Duration, and Adolescent Myopia: A NHANES Cross-Sectional Study with Implications for Ocular Photodiagnostic ScreeningZhixing Xu, Dingyan Chen, Zhengyang Tao, et al.
Frontiers in Pediatrics|April 16, 2020
A Synonymous Variant c.579A>G in the ETFDH Gene Caused Exon Skipping in a Patient With Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Case ReportGuorui Hu, Jingxia Zeng, Chunli Wang, et al.
Annals of Medicine|October 1, 2025
Tracking myopia development through axial length progression: a retrospective longitudinal studyZhengyang Tao, Jiao Wang, Zongyue Lv, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Translational Pediatrics|November 11, 2024
Significance of binocular fusion in enhancing visual acuity during amblyopia treatmentZongyue Lv, Zhengyang Tao, Guorui Hu, et al.
BMC Pediatrics|October 17, 2014
Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysisBixia Zheng, Guorui Hu, Jin Yu, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|April 13, 2022
Machine Learning-Based Perihematomal Tissue Features to Predict Clinical Outcome after Spontaneous Intracerebral HemorrhageXin Qi, Guorui Hu, Haiyan Sun, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 25, 2022
[Genetic analysis of PYGL gene variants for a child with Glycogen storage disease VI]Yucan Zheng, Guiping Kong, Guorui Hu, et al.
Gene|March 1, 2026
A novel variant in ARID2 causes Coffin-Siris syndrome 6 with liver cirrhosisXueying Qian, Yvcan Zheng, Liqian Zhao, et al.
Molecular Medicine Reports|June 28, 2014
Diagnosis of ABCB11 gene mutations in children with intrahepatic cholestasis using high resolution melting analysis and direct sequencingGuorui Hu, Ping He, Zhifeng Liu, et al.
Journal of Colloid and Interface Science|December 17, 2025
Catalytic vs. thermal Si - H crosslinking polydimethylsiloxane (PDMS) elastomers: Network heterogeneity drives interfacial performanceZiheng Chen, Yongjie Gao, Guorui Hu, et al.
Photodiagnosis and Photodynamic Therapy|May 29, 2026
Sleep Quality, Sleep Duration, and Adolescent Myopia: A NHANES Cross-Sectional Study with Implications for Ocular Photodiagnostic ScreeningZhixing Xu, Dingyan Chen, Zhengyang Tao, et al.
Frontiers in Pediatrics|April 16, 2020
A Synonymous Variant c.579A>G in the ETFDH Gene Caused Exon Skipping in a Patient With Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Case ReportGuorui Hu, Jingxia Zeng, Chunli Wang, et al.
Annals of Medicine|October 1, 2025
Tracking myopia development through axial length progression: a retrospective longitudinal studyZhengyang Tao, Jiao Wang, Zongyue Lv, et al.
Pageof 3