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BMC Ophthalmology|October 27, 2016
Bilateral abducens nerve palsy in an infant case of fulminant acute disseminated encephalomyelitis: a case reportZhiliang Yang, Guilian SunScientific Reports|October 25, 2017
High-frequency, low-coverage "false positives" mutations may be true in GS Junior sequencing studiesZhiliang Yang, Guilian SunEpilepsy & Behavior Case Reports|November 11, 2016
Headache maybe the initial symptom in Rasmussen's syndrome: A child case reportZhiliang Yang, Guilian SunJournal of Neural Transmission (Vienna, Austria : 1996)|February 21, 2014
Association of MDR1 gene C3435T polymorphism with childhood intractable epilepsy: a meta-analysisGuilian Sun, Xue Sun, Limei GuanJournal of Pediatric Hematology/Oncology|November 6, 2019
A Pediatric Case Report of Epstein-Barr Virus-associated Hemophagocytic Lymphohistiocytosis With Pericardial Effusion and Multiple Coronary Artery AneurysmsGuilian Sun, Fang Yao, Zhiliang YangPlants (Basel, Switzerland)|October 14, 2023
Transcriptome Analysis Reveals Candidate Genes Involved in Gibberellin-Induced Fruit Development in <i>Rosa roxburghii</i>Xiaolong Huang, Xiaoai Wu, Guilian Sun, et al.BMC Medical Genetics|October 5, 2018
A first CLN6 variant case of late infantile neuronal ceroid lipofuscinosis caused by a homozygous mutation in a boy from China: a case reportGuilian Sun, Fang Yao, Zhuoling Tian, et al.BMC Medical Genetics|October 8, 2017
A novel compound mutation in GLRA1 cause hyperekplexia in a Chinese boy- a case report and review of the literatureZhiliang Yang, Guilian Sun, Fang Yao, et al.The Journal of Pathology|September 2, 2003
Platelet-derived growth factor and its receptors are related to the progression of human muscular dystrophy: an immunohistochemical studyYajuan Zhao, Kazuhiro Haginoya, Guilian Sun, et al.Carbohydrate Polymers|June 15, 2023
Human milk oligosaccharide lacto-N-tetraose: Physiological functions and synthesis methodsMiaomiao Hu, Ming Miao, Kewen Li, et al.Pageof 3