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Shan Tang

Showing results (581-590 of 595) with videos related to

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Epilepsia|November 6, 2015
The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndromeJan Larsen, Katrine Marie Johannesen, Jakob Ek, et al.
Cell Calcium|January 13, 2022
Mutations and clinical significance of calcium voltage-gated channel subunit alpha 1E (CACNA1E) in non-small cell lung cancerSan-Hui Gao, Gui-Zhen Wang, Li-Peng Wang, et al.
Epilepsy & Behavior : E&B|November 19, 2015
Risk factors for reading disability in families with rolandic epilepsyYaiza Hernández Vega, Anna Smith, Hannah Cockerill, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|November 21, 2020
Impact of 9-Minute Withdrawal Time on the Adenoma Detection Rate: A Multicenter Randomized Controlled TrialShengbing Zhao, Xia Yang, Shuling Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 22, 2022
Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort studyJia-Lu Liu, Xiao-Wen Wang, Cui-Hua Liu, et al.
BMJ Open|December 3, 2025
Steerable versus Conventional flexible and navigable suction ureteral access sheath (FANS) flexible Ureteroscopy for Lower Pole stones Treatment: study protocol for a multicentre, randomised superiority trial (SCULPT trial)Steffi Kar Kei Yuen, Shusheng Liu, Vineet Gauhar, et al.
Epilepsia|May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizuresShan Tang, Laura Addis, Anna Smith, et al.
Cancers|August 30, 2020
Systems Biology Approach Identifies Prognostic Signatures of Poor Overall Survival and Guides the Prioritization of Novel BET-CHK1 Combination Therapy for OsteosarcomaPankita H Pandya, Lijun Cheng, M Reza Saadatzadeh, et al.
World Journal of Pediatrics : WJP|June 1, 2021
Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease DatabaseJia-Lu Liu, Qian Shen, Ming-Yan Wu, et al.
Cell Proliferation|October 19, 2023
Human neural stem cellsYu-Kai Wang, Juan Yu, Ting-Ting Zhang, et al.
Pageof 60

Showing results (581-590 of 595) with videos related to

Sort By:
Pageof 60
Epilepsia|November 6, 2015
The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndromeJan Larsen, Katrine Marie Johannesen, Jakob Ek, et al.
Cell Calcium|January 13, 2022
Mutations and clinical significance of calcium voltage-gated channel subunit alpha 1E (CACNA1E) in non-small cell lung cancerSan-Hui Gao, Gui-Zhen Wang, Li-Peng Wang, et al.
Epilepsy & Behavior : E&B|November 19, 2015
Risk factors for reading disability in families with rolandic epilepsyYaiza Hernández Vega, Anna Smith, Hannah Cockerill, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|November 21, 2020
Impact of 9-Minute Withdrawal Time on the Adenoma Detection Rate: A Multicenter Randomized Controlled TrialShengbing Zhao, Xia Yang, Shuling Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 22, 2022
Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort studyJia-Lu Liu, Xiao-Wen Wang, Cui-Hua Liu, et al.
BMJ Open|December 3, 2025
Steerable versus Conventional flexible and navigable suction ureteral access sheath (FANS) flexible Ureteroscopy for Lower Pole stones Treatment: study protocol for a multicentre, randomised superiority trial (SCULPT trial)Steffi Kar Kei Yuen, Shusheng Liu, Vineet Gauhar, et al.
Epilepsia|May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizuresShan Tang, Laura Addis, Anna Smith, et al.
Cancers|August 30, 2020
Systems Biology Approach Identifies Prognostic Signatures of Poor Overall Survival and Guides the Prioritization of Novel BET-CHK1 Combination Therapy for OsteosarcomaPankita H Pandya, Lijun Cheng, M Reza Saadatzadeh, et al.
World Journal of Pediatrics : WJP|June 1, 2021
Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease DatabaseJia-Lu Liu, Qian Shen, Ming-Yan Wu, et al.
Cell Proliferation|October 19, 2023
Human neural stem cellsYu-Kai Wang, Juan Yu, Ting-Ting Zhang, et al.
Pageof 60