Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Ji-qing Cao"'
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 20, Iss 6, Pp 534-540 (2020)
Objective To explore the diversity of clinical manifestations and gene mutations of riboflavin⁃responsive multiple acyl⁃coenzyme A dehydrogenase deficiency (MADD). Methods and Results The clinical, blood biochemical, EMG, muscle biopsy and geneti
Externí odkaz:
https://doaj.org/article/045033e3909e49f4b097627d3d3025a0
Autor:
Ji-qing Cao, Ying-yin Liang, Ya-qin Li, Hui-li Zhang, Yu-ling Zhu, Jia Geng, Li-qing Yang, Shan-wei Feng, Juan Yang, Jie Kong, Cheng Zhang
Publikováno v:
Neural Regeneration Research, Vol 11, Iss 10, Pp 1638-1643 (2016)
Adipose-derived stem cells have been shown to promote peripheral nerve regeneration through the paracrine secretion of neurotrophic factors. However, it is unclear whether these cells can promote myogenic differentiation in muscular dystrophy. Adipos
Externí odkaz:
https://doaj.org/article/389b50d152e84bfa895a42550bca8a41
Autor:
Juan YANG, Hui-fang XIE, Ji-qing CAO, Hui ZHENG, Can-quan ZHOU, Zhen-hua LIU, Yu-ling ZHU, Yi-xin ZHAN, Xiao-ting SHEN, Ya-qin LI, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 15, Iss 6, Pp 458-463 (2015)
Objective To carry out preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) carrier, so as to prevent the birth of affected infants with DMD. Methods One DMD gene carrier with a deletion of exon 10-30 received fertilization w
Externí odkaz:
https://doaj.org/article/48f9fa8c71004e839157878b42ad66e2
Autor:
Ji-qing CAO, Juan YANG, Ya-qin LI, Shan-wei FENG, Fei CHEN, Hui ZHENG, Ying-yin LIANG, Bao-jian ZHAO, Xu ZHANG, Hui-li ZHANG, Yu-ling ZHU, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 15, Iss 6, Pp 442-447 (2015)
Background DMD gene point mutation, mainly nonsense mutation, always cause the most severe Duchenne muscular dystrophy (DMD). However, we also observed some cases of Becker muscular dystrophy (BMD) carrying DMD point mutation. This paper aims to expl
Externí odkaz:
https://doaj.org/article/50a62ecc4b2d4cb3a357677a35a5ef25
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 15, Iss 6, Pp 437-441 (2015)
Objective Use T2 mapping to evaluate the fatty infiltration of thigh muscles in Duchenne muscular dystrophy (DMD) patients, so as to analyze the value of T2 mapping and T2 relaxation time in the diagnosis of DMD. Methods Sixteen DMD patients who were
Externí odkaz:
https://doaj.org/article/be7ee3b57b174b50a149b375eb4cf886
Autor:
Ji-qing CAO, Cheng ZHANG, Ya-qin LI, Juan YANG, Ying-yin LIANG, Shan-wei FENG, Xu ZHANG, Jing LI, Hui-li ZHANG, Yu-ling ZHU, Jia GENG, Li-qing YANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 14, Iss 6, Pp 479-484 (2014)
Objective The clinical manifestation and electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation of riboflavin-responsive lipid storage myopathy were analyzed for early diagnosis and treatment.mutation of riboflavin-responsive lipid storag
Externí odkaz:
https://doaj.org/article/fe0465402f494326bae6a2d1de7d572d
Autor:
Hui-li ZHANG, Yi-ming SUN, Min-ying ZHENG, Yu-ling ZHU, Ji-qing CAO, Yu ZHANG, Ya-qin LI, Lang-hui DENG, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 14, Iss 6, Pp 490-495 (2014)
Background To investigate the gene mutation and clinical features of hypokalemic periodic paralysis (HypoPP) in a Han family. Methods Mutation analyses of CACNA1S, SCN4A and KCNE3 gene were screened by DNA direct sequencing in the proband (Ⅲ3). The
Externí odkaz:
https://doaj.org/article/ca4ff0eeda5b47868b5400eebd75b0a4
Autor:
Juan YANG, Ji-qing CAO, Zhen-hua LIU, Yi-xin ZHAN, Ying-yin LIANG, Gui-ling MO, Ya-qin LI, Yi-ming SUN, Min-zi LI, Jing LI, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 14, Iss 5, Pp 405-410 (2014)
Objective In order to make a well understanding on glycogen storage disease typeⅡ (GSDⅡ), this paper explored clinical features and genetic analysis of 7 patients with late-onset glycogen storage disease typeⅡ. Methods Clinical data of 7 patien
Externí odkaz:
https://doaj.org/article/e6308a0d0ff94917b03389c7e0c5554b
Autor:
Juan YANG, Wei-xun FENG, Ji-qing CAO, Yan-yun WANG, Ya-qin LI, Shi-biao HUANG, Yan-jun LUO, Zhuo-lin LIU, Yi-ming SUN, Zhen-hua LIU, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 14, Iss 5, Pp 411-415 (2014)
Objective To evaluate the effect of Myozyme on one ventilator dependent patient with late-onset glycogen storage disease typeⅡ (GSDⅡ). Methods Myozyme infusion was administered based on manufacturer's recommendations at 20 mg/kg every 2 to 4 week
Externí odkaz:
https://doaj.org/article/23360398e24f4b08b64ef03b08b65103
Autor:
Jing LI, Cheng ZHANG, Yi⁃xin ZHANG, Shan⁃wei FENG, Juan YANG, Ji⁃qing CAO, Chang⁃shun YU, Ya⁃qin LI, Yan⁃yun WANG, Fei CHEN, Jie KONG, Min⁃ying ZHENG, Ling LIAO
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 12, Iss 3, Pp 282-287 (2012)
Objective To explore the clinical features, genetic characters and the importance of prenatal diagnosis in spinocerebellar ataxia 3 (SCA3) patients. Methods SCA3/ATXN3 gene was determined by using PCR and segmental analysis techniques in 2 patients a
Externí odkaz:
https://doaj.org/article/8976d63864d64f41bb273f938c0e28a5