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Tian-Fu Li

Showing results (11-20 of 27) with videos related to

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World Neurosurgery|May 20, 2018
Asymmetry of Cerebral Peduncles for Predicting Motor Function Restoration in Young Patients Before HemispherectomyXiu-Yu Du, Si-Chang Chen, Yu-Guang Guan, et al.
Epilepsia Open|September 9, 2022
The long-term surgical outcomes of low-grade epilepsy-associated neuroepithelial tumorsMing-Guo Xie, Xiong-Fei Wang, Jiao Qiao, et al.
BMC Urology|December 23, 2014
46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literatureTian-Fu Li, Qiu-Yue Wu, Cui Zhang, et al.
Molecular Medicine Reports|August 12, 2015
A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature reviewXin-Yi Xia, Cui Zhang, Tian-Fu Li, et al.
Epilepsy & Behavior : E&B|June 11, 2021
Regulation of TWIK-related K<sup>+</sup> channel 1 in the anterior hippocampus of patients with temporal lobe epilepsy with comorbid depressionXiao-Li Li, Chong-Yang Tang, Shu Wang, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|June 10, 2014
[Therapeutic efficacy of compound Xuanju capsule on autoimmune prostatitis in rats: an experimental study]Tian-Fu Li, Qiu-Yue Wu, Wei-Wei Li, et al.
Cancer Cell International|April 24, 2020
Overexpression of kinesin superfamily members as prognostic biomarkers of breast cancerTian-Fu Li, Hui-Juan Zeng, Zhen Shan, et al.
Clinical Neurology and Neurosurgery|August 6, 2024
The long-term outcomes in drug-resistant epilepsy patients who underwent subtotal hemispherotomy: A single-center retrospective cohort studyTian-Yi Cui, Wei Luan, Chong-Yang Tang, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|December 18, 2013
[Detection of DPY19L2 gene mutation in a globozoospermia patient]Qiu-Yue Wu, Na Li, Tian-Fu Li, et al.
BMC Medical Genetics|August 16, 2014
A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese familyXin-Yi Xia, Na Li, Xiang Cao, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
World Neurosurgery|May 20, 2018
Asymmetry of Cerebral Peduncles for Predicting Motor Function Restoration in Young Patients Before HemispherectomyXiu-Yu Du, Si-Chang Chen, Yu-Guang Guan, et al.
Epilepsia Open|September 9, 2022
The long-term surgical outcomes of low-grade epilepsy-associated neuroepithelial tumorsMing-Guo Xie, Xiong-Fei Wang, Jiao Qiao, et al.
BMC Urology|December 23, 2014
46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literatureTian-Fu Li, Qiu-Yue Wu, Cui Zhang, et al.
Molecular Medicine Reports|August 12, 2015
A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature reviewXin-Yi Xia, Cui Zhang, Tian-Fu Li, et al.
Epilepsy & Behavior : E&B|June 11, 2021
Regulation of TWIK-related K<sup>+</sup> channel 1 in the anterior hippocampus of patients with temporal lobe epilepsy with comorbid depressionXiao-Li Li, Chong-Yang Tang, Shu Wang, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|June 10, 2014
[Therapeutic efficacy of compound Xuanju capsule on autoimmune prostatitis in rats: an experimental study]Tian-Fu Li, Qiu-Yue Wu, Wei-Wei Li, et al.
Cancer Cell International|April 24, 2020
Overexpression of kinesin superfamily members as prognostic biomarkers of breast cancerTian-Fu Li, Hui-Juan Zeng, Zhen Shan, et al.
Clinical Neurology and Neurosurgery|August 6, 2024
The long-term outcomes in drug-resistant epilepsy patients who underwent subtotal hemispherotomy: A single-center retrospective cohort studyTian-Yi Cui, Wei Luan, Chong-Yang Tang, et al.
Zhonghua Nan Ke Xue = National Journal of Andrology|December 18, 2013
[Detection of DPY19L2 gene mutation in a globozoospermia patient]Qiu-Yue Wu, Na Li, Tian-Fu Li, et al.
BMC Medical Genetics|August 16, 2014
A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese familyXin-Yi Xia, Na Li, Xiang Cao, et al.
Pageof 3