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Human Vaccines & Immunotherapeutics
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March 30, 2026
DTaP-induced infantile epileptic spasms syndrome high-risk window: Insights from school-age children
Qi Zhang, Wen He, Meng-Na Zhang, et al.
Medicine
|
January 26, 2017
Clinical features of benign epilepsy of childhood with centrotemporal spikes in chinese children
Meng-Jia Liu, Xiao-Jun Su, Xiu-Yu Shi Md, et al.
Science Bulletin
|
July 18, 2024
Phase I clinical trial of intracerebral injection of lentiviral-ABCD1 for the treatment of cerebral adrenoleukodystrophy
Qiu-Hong Wang, Jing Wang, Zhi-Pei Ling, et al.
Environmental Health and Preventive Medicine
|
November 19, 2009
A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians
Wanyang Liu, Hirokuni Hashikata, Kayoko Inoue, et al.
Radiology
|
March 28, 2018
Alterations of White Matter Connectivity in Preschool Children with Autism Spectrum Disorder
Shi-Jun Li, Yi Wang, Long Qian, et al.
Orphanet Journal of Rare Diseases
|
August 15, 2024
Long-term safety and influence on growth in patients receiving sirolimus: a pooled analysis
Yang-Yang Wang, Li-Ping Zou, Kai-Feng Xu, et al.
Chinese Medical Journal
|
November 18, 2011
Prospective, naturalistic study of open-label OROS methylphenidate treatment in Chinese school-aged children with attention-deficit/hyperactivity disorder
Yi Zheng, Yu-Feng Wang, Jiong Qin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 26, 2018
Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorder
Shi-Jun Li, Shan-Shan Yu, Hong-Yu Luo, et al.
Ebiomedicine
|
June 25, 2020
Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population
Xiu-Yu Shi, Geng Wang, Ting Li, et al.
Brain : a Journal of Neurology
|
March 4, 2023
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment
Fang Liu, Chen Liang, Zhengchang Li, et al.
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Search research articles
Search
Showing results (171-180 of 181) with videos related to
Sort By:
Page
of 19
Human Vaccines & Immunotherapeutics
|
March 30, 2026
DTaP-induced infantile epileptic spasms syndrome high-risk window: Insights from school-age children
Qi Zhang, Wen He, Meng-Na Zhang, et al.
Medicine
|
January 26, 2017
Clinical features of benign epilepsy of childhood with centrotemporal spikes in chinese children
Meng-Jia Liu, Xiao-Jun Su, Xiu-Yu Shi Md, et al.
Science Bulletin
|
July 18, 2024
Phase I clinical trial of intracerebral injection of lentiviral-ABCD1 for the treatment of cerebral adrenoleukodystrophy
Qiu-Hong Wang, Jing Wang, Zhi-Pei Ling, et al.
Environmental Health and Preventive Medicine
|
November 19, 2009
A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians
Wanyang Liu, Hirokuni Hashikata, Kayoko Inoue, et al.
Radiology
|
March 28, 2018
Alterations of White Matter Connectivity in Preschool Children with Autism Spectrum Disorder
Shi-Jun Li, Yi Wang, Long Qian, et al.
Orphanet Journal of Rare Diseases
|
August 15, 2024
Long-term safety and influence on growth in patients receiving sirolimus: a pooled analysis
Yang-Yang Wang, Li-Ping Zou, Kai-Feng Xu, et al.
Chinese Medical Journal
|
November 18, 2011
Prospective, naturalistic study of open-label OROS methylphenidate treatment in Chinese school-aged children with attention-deficit/hyperactivity disorder
Yi Zheng, Yu-Feng Wang, Jiong Qin, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 26, 2018
Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorder
Shi-Jun Li, Shan-Shan Yu, Hong-Yu Luo, et al.
Ebiomedicine
|
June 25, 2020
Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population
Xiu-Yu Shi, Geng Wang, Ting Li, et al.
Brain : a Journal of Neurology
|
March 4, 2023
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment
Fang Liu, Chen Liang, Zhengchang Li, et al.
Page
of 19