Search Results - Chunquan Cai

Review on neuroimaging in pediatric-type diffuse low-grade gliomas by Jing Chen, Xin Qi, Mengjie Zhang, Jing Zhang, Tong Han, Chunxiang Wang, Chunquan Cai, Chunquan Cai

Connect to this object online.

Case Report: Recurrent Hemiplegic Migraine Attacks Accompanied by Intractable Hypomagnesemia Due to a de novo TRPM7 Gene Variant by Meifang Lei, Ping Wang, Ping Wang, Hong Li, Xiaojun Liu, Jianbo Shu, Jianbo Shu, Qianqian Zhang, Chunquan Cai, Chunquan Cai, Chunquan Cai, Dong Li, Yuqin Zhang

Connect to this object online.

Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients by Ping Wang, Ping Wang, Jianbo Shu, Jianbo Shu, Chunyu Gu, Chunyu Gu, Chunyu Gu, Xiaoli Yu, Jie Zheng, Jie Zheng, Chunhua Zhang, Chunquan Cai, Chunquan Cai, Chunquan Cai

Connect to this object online.

Case Report: A Case of β-Ureidopropionase Deficiency Complicated With MELAS Syndrome Caused by UPB1 Variant and Mitochondrial Gene Variant by Jianbo Shu, Jianbo Shu, Jianbo Shu, Xiufang Zhi, Xiufang Zhi, Jing Chen, Jing Chen, Meifang Lei, Meifang Lei, Jie Zheng, Jie Zheng, Wenchao Sheng, Wenchao Sheng, Chunhua Zhang, Dong Li, Dong Li, Chunquan Cai, Chunquan Cai, Chunquan Cai, Chunquan Cai

Connect to this object online.

Case Report: A developmental and epileptic encephalopathy 45 due to de novo variant of GABRB1 by Lu Wang, Lu Wang, Haiquan Xu, Jianbo Shu, Jianbo Shu, Dandan Yan, Dandan Yan, Dong Li, Chunquan Cai, Chunquan Cai

Connect to this object online.

Clinical and Magnetic Resonance Imaging Characteristics of Pediatric Acute Disseminating Encephalomyelitis With and Without Antibodies to Myelin Oligodendrocyte Glycoprotein by Meifang Lei, Yaqiong Cui, Yaqiong Cui, Zhaoying Dong, Xiufang Zhi, Xiufang Zhi, Jianbo Shu, Jianbo Shu, Chunquan Cai, Chunquan Cai, Dong Li

Connect to this object online.

Vitamin D levels and Vitamin D-related gene polymorphisms in Chinese children with type 1 diabetes by Xiaofang Chen, Xiaofang Chen, Jia Fu, Jia Fu, Ying Qian, Ying Qian, Xiufang Zhi, Xiufang Zhi, Linjie Pu, Linjie Pu, Chunyu Gu, Chunyu Gu, Jianbo Shu, Jianbo Shu, Jianbo Shu, Ling Lv, Ling Lv, Chunquan Cai, Chunquan Cai, Chunquan Cai

Connect to this object online.

High-throughput screening reveals novel mutations in spinal muscular atrophy patients by Ruiping Zhang, Chunyu Gu, Linjie Pu, Yingtao Meng, Jianbo Shu, Chunquan Cai

Connect to this object online.

Case Report: Cardiac Multiple Thrombus and Pulmonary Embolism Associated With Mycoplasma Pneumonia Infection in a Child by Tongqiang Zhang, Jiafeng Zheng, Hongbo Wang, Yongsheng Xu, Jing Ning, Chunquan Cai

Connect to this object online.

Complicated Hereditary Spastic Paraplegia Caused by SERAC1 Variants in a Chinese Family by Dandan Yan, Dandan Yan, Shaopei Chen, Fengying Cai, Jianbo Shu, Jianbo Shu, Xiufang Zhi, Xiufang Zhi, Jie Zheng, Jie Zheng, Chunhua Zhang, Dong Li, Chunquan Cai, Chunquan Cai

Connect to this object online.

Case Report: Clinical Analysis of Fulminant Mycoplasma pneumoniae Pneumonia in Children by Tongqiang Zhang, Chunjiao Han, Wei Guo, Wei Guo, Jing Ning, Chunquan Cai, Yongsheng Xu

Connect to this object online.

Correlation of tuberculosis-related anemia severity with tuberculosis-induced inflammation in children: a six-year retrospective study by Chunjiao Han, Yulian Fang, Lili Dong, Detong Guo, Min Lei, Wei Guo, Chunquan Cai

Connect to this object online.

The biallelic novel pathogenic variants in AGL gene in a chinese patient with glycogen storage disease type III by Jing Wang, Yuping Yu, Chunquan Cai, Xiufang Zhi, Ying Zhang, Yu Zhao, Jianbo Shu

Connect to this object online.

A novel missense in GLI3 possibly affecting one of the zinc finger domains may lead to postaxial synpolydactyly: case report by Qianqian Zou, Zhigang Tian, Jie Zheng, Xiufang Zhi, Xiaojie Du, Jianbo Shu, Chunquan Cai

Connect to this object online.

Beware of missed diagnosis in patients with multiple genetic diseases: a case report by Detong Guo, Xuemei Li, Nan Liu, Xiaoli Yu, Jianbo Shu, Wenchao Sheng, Dong Li, Chunquan Cai

Connect to this object online.

What is the impact of a novel DEPDC5 variant on an infant with focal epilepsy: a case report by Chunyu Gu, Xiaowei Lu, Jinhui Ma, Linjie Pu, Xiufang Zhi, Jianbo Shu, Dong Li, Chunquan Cai

Connect to this object online.

Whole-exome sequencing as the first-tier test for patients in neonatal intensive care unit: a Chinese single-center study by Ruiping Zhang, Xiaoyu Cui, Yan Zhang, Huiqing Ma, Jing Gao, Ying Zhang, Jianbo Shu, Chunquan Cai, Yang Liu

Connect to this object online.

Successful treatment of pleural empyema and necrotizing pneumonia caused by methicillin-resistant Staphylococcus aureus infection following influenza A virus infection: A case repo... by Chunjiao Han, Chunjiao Han, Tongqiang Zhang, Yidi Zhao, Lili Dong, Xiaole Li, Jiafeng Zheng, Wei Guo, Yongsheng Xu, Chunquan Cai

Connect to this object online.

Clinical diagnosis and mutation analysis of four Chinese families with succinic semialdehyde dehydrogenase deficiency by Ping Wang, Fengying Cai, Lirong Cao, Yizheng Wang, Qianqian Zou, Peng Zhao, Chao Wang, Yuqin Zhang, Chunquan Cai, Jianbo Shu

Connect to this object online.

Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of <i>CTTNBP2</i> in a Quad Family Affected by Autism Spectrum Disorder by Yingmei Xie, Hui Wang, Bing Hu, Xueli Zhang, Aiping Liu, Chunquan Cai, Shijun Li, Cheng Chen, Zhangxing Wang, Zhaoqing Yin, Mingbang Wang

Connect to this object online.