Search Results - Kaili Shi

CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of Phenotypes by Linxia Zhang, Linxia Zhang, Yongxin Wen, Qingping Zhang, Yan Chen, Jiaping Wang, Kaili Shi, Lijun Du, Xinhua Bao

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Crohn's disease after multiple doses of rituximab treatment in a child with refractory nephrotic syndrome and an ATG2A mutation: a case report by Kaili Shi, Mengzhen Fu, Wei Xia, Pei Zhang, Pei Zhang, Chunlin Gao, Chunlin Gao, Zhengkun Xia, Zhengkun Xia

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A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: clinical course and response to riboflavin by Kaili Shi, Zhen Shi, Huifang Yan, Xiaodong Wang, Yanling Yang, Hui Xiong, Qiang Gu, Ye Wu, Yuwu Jiang, Jingmin Wang

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Levetiracetam may be an unsuitable choice for patients with PRRT2-associated self-limited infantile epilepsy by Yang Tian, Zhen Shi, Jiahao Cai, Chi Hou, Xiuying Wang, Haixia Zhu, Binwei Peng, Kaili Shi, Xiaojing Li, Sitang Gong, Wen-Xiong Chen

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Serum IgE levels are a risk factor with prognosis of pediatric minimal change disease by Tingting Han, Tingting Han, Mei Xue, Yafei Guan, Yafei Guan, Tao Ju, Kaili Shi, Mengzhen Fu, Lili Jia, Chunlin Gao, Chunlin Gao, Zhengkun Xia, Zhengkun Xia

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