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Sha Tang

Showing results (101-110 of 448) with videos related to

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Frontiers in Medicine|November 4, 2022
Clinical features and prognostic factors of pulmonary carcinosarcoma: A nomogram development and validation based on surveillance epidemiology and end results databaseMing-Yi Zhang, Lian-Sha Tang, Zhao-Juan Qin, et al.
Clinical Case Reports|July 11, 2018
Diagnostic exome sequencing identifies <i>GLI2</i> haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomaliesSamin A Sajan, Zöe Powis, Katherine L Helbig, et al.
Zhonghua Nei Ke Za Zhi|July 13, 2005
[The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family]Ya-wei Shen, Bei-sha Tang, Xin-xiang Yan, et al.
International Journal of Colorectal Disease|July 5, 2022
Clinical characteristics and prognostic factors of anal adenocarcinoma: a nomogram development based on SEER database and validation in the WCH databaseYu-Wen Zhou, Gui-Xia Wei, Lian-Sha Tang, et al.
Chinese Medical Journal|September 14, 2020
Clinical and genetic features of transthyretin-related familial amyloid polyneuropathy in ChinaLei Liu, Xiao-Bo Li, Zheng-Mao Hu, et al.
Neurobiology of Aging|September 6, 2014
Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2Chaodong Wang, Yanming Xu, Xiuli Feng, et al.
Rare Diseases (Austin, Tex.)|July 9, 2014
Mutation in SNAP25 as a novel genetic cause of epilepsy and intellectual disabilityLuis Rohena, Julie Neidich, Megan Truitt Cho, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 9, 2015
The contribution of GIGYF2 to Parkinson's disease: a meta-analysisYuan Zhang, Qi-Ying Sun, Ren-He Yu, et al.
Chinese Medical Journal|July 22, 2004
Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese casesBei-sha Tang, Xin Chen, Guo-hua Zhao, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 27, 2014
Non-motor symptoms in Chinese Parkinson's disease patients with and without LRRK2 G2385R and R1628P variantsDa-Wei Li, Zhuqin Gu, Chaodong Wang, et al.
Pageof 45

Showing results (101-110 of 448) with videos related to

Sort By:
Pageof 45
Frontiers in Medicine|November 4, 2022
Clinical features and prognostic factors of pulmonary carcinosarcoma: A nomogram development and validation based on surveillance epidemiology and end results databaseMing-Yi Zhang, Lian-Sha Tang, Zhao-Juan Qin, et al.
Clinical Case Reports|July 11, 2018
Diagnostic exome sequencing identifies <i>GLI2</i> haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomaliesSamin A Sajan, Zöe Powis, Katherine L Helbig, et al.
Zhonghua Nei Ke Za Zhi|July 13, 2005
[The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family]Ya-wei Shen, Bei-sha Tang, Xin-xiang Yan, et al.
International Journal of Colorectal Disease|July 5, 2022
Clinical characteristics and prognostic factors of anal adenocarcinoma: a nomogram development based on SEER database and validation in the WCH databaseYu-Wen Zhou, Gui-Xia Wei, Lian-Sha Tang, et al.
Chinese Medical Journal|September 14, 2020
Clinical and genetic features of transthyretin-related familial amyloid polyneuropathy in ChinaLei Liu, Xiao-Bo Li, Zheng-Mao Hu, et al.
Neurobiology of Aging|September 6, 2014
Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2Chaodong Wang, Yanming Xu, Xiuli Feng, et al.
Rare Diseases (Austin, Tex.)|July 9, 2014
Mutation in SNAP25 as a novel genetic cause of epilepsy and intellectual disabilityLuis Rohena, Julie Neidich, Megan Truitt Cho, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 9, 2015
The contribution of GIGYF2 to Parkinson's disease: a meta-analysisYuan Zhang, Qi-Ying Sun, Ren-He Yu, et al.
Chinese Medical Journal|July 22, 2004
Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese casesBei-sha Tang, Xin Chen, Guo-hua Zhao, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 27, 2014
Non-motor symptoms in Chinese Parkinson's disease patients with and without LRRK2 G2385R and R1628P variantsDa-Wei Li, Zhuqin Gu, Chaodong Wang, et al.
Pageof 45