Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Guo‐Rong Xu"'
Autor:
Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Hai-Zhu Chen, Min-Ting Lin, Nai-Qing Cai, Ming Jin, Liu-Qing Xu, Wei Hu, Ning Wang, Zhi-Qiang Wang, Li-Shao Guo
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 22, Pp 2753-2755 (2021)
Externí odkaz:
https://doaj.org/article/eecb6fd1948e4082a8be5b5932908fe6
Autor:
Hai-Zhu Chen, Ming Jin, Nai-Qing Cai, Xiao-Dan Lin, Xin-Yi Liu, Liu-Qing Xu, Min-Ting Lin, Feng Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu, Yi Cui
Publikováno v:
Chinese Medical Journal, Vol 132, Iss 13, Pp 1615-1618 (2019)
Externí odkaz:
https://doaj.org/article/2fff0e1a423c42e1902353678b37ef51
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Objective: To explore the associations between serum uric acid levels with survival in male and female ALS patients.Methods: A longitudinal cohort study was carried out including 313 sporadic and 16 familial ALS patients with repeated serum uric acid
Externí odkaz:
https://doaj.org/article/dcb1a947685a4256a95bb00b01740b86
Autor:
Liu-Qing Xu, Wei Hu, Qi-Fu Guo, Lu-Lu Lai, Guo-Rong Xu, Wan-Jin Chen, Ning Wang, Qi-Jie Zhang
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Objective: This study aims to explore the association between median nerve-neurophysiological index (NI) and survival of patients with amyotrophic lateral sclerosis (ALS).Methods: A retrospective case series with a prospective follow-up study was per
Externí odkaz:
https://doaj.org/article/11977fb54d8d4024b843a0dcf9799bf4
Autor:
Guo-rong Xu, Wei Hu, Ling-Ling Zhan, Chong Wang, Liu-Qing Xu, Min-Ting Lin, Wan-Jin Chen, Ning Wang, Qi-Jie Zhang
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Amyotrophic lateral sclerosis (ALS) is a devastating motor neuron disease characterized by substantial clinical and genetic heterogeneity. Thus far, only a few TARDBP-ALS families have been reported in China, and no mutation analy
Externí odkaz:
https://doaj.org/article/8bbc57cb79074505866eef6165591f24
Autor:
Xiao-Dan Lin, Jun-Jie He, Feng Lin, Hai-Zhu Chen, Liu-Qing Xu, Wei Hu, Nai-Qing Cai, Min-Ting Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 18, Pp 2164-2171 (2018)
Background: Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric muscular deficit of facial, shoulder-girdle muscles, and descending to lower limb muscles, but it exists in several extramuscular manifestations or overlapping s
Externí odkaz:
https://doaj.org/article/e16c5af090ef4ddcb0ee68da2b7a287f
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 17, Iss 8, Pp 603-608 (2017)
Background Owing to the clinical variability and molecular heterogeneity, the traditional Sanger sequencing takes time and effort and is inefficient. In this paper, target region capture sequencing in the diagnosing of autosomal recessive Charcot-Mar
Externí odkaz:
https://doaj.org/article/dd8b6b4927e2422487545c6a92d67d73
Biallelic variants in the COQ7 gene cause distal hereditary motor neuropathy in two Chinese families
Autor:
Xiao-xuan Liu, Ning Wang, Yi-kun Chen, Wen-qi Lv, Jing-Mei Hong, Guo-Rong Xu, Lin-Ying Zhou, Wan-Jin Chen, Dong-Sheng Fan, Jin He
Publikováno v:
Brain. 146:e27-e30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8174fae661356b204cf7f6da267c0334
https://doi.org/10.1093/brain/awad040
https://doi.org/10.1093/brain/awad040
Autor:
Yi‐Heng Zeng, Kang Yang, Gan‐Qin Du, Yi‐Kun Chen, Chun‐Yan Cao, Yu‐Sen Qiu, Jin He, Hai‐Dong Lv, Qian‐Qian Qu, Jian‐Nan Chen, Guo‐Rong Xu, Long Chen, Fu‐Ze Zheng, Miao Zhao, Min‐Ting Lin, Wan‐Jin Chen, Jing Hu, Zhi‐Qiang Wang, Ning Wang
Publikováno v:
Annals of Neurology. 92:512-526
Oculopharyngodistal myopathy (OPDM) is an adult-onset neuromuscular disease characterized by progressive ptosis, dysarthria, ophthalmoplegia, and distal muscle weakness. Recent studies revealed that GGC repeat expansions in 5'-UTR of LRP12, GIPC1, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd83a57931a3880691cc67a60eed3ee9
https://doi.org/10.1002/ana.26436
https://doi.org/10.1002/ana.26436
Autor:
Jin He, Xiao‐Xuan Liu, Ming‐Ming Ma, Jing‐Jing Lin, Jun Fu, Yi‐Kun Chen, Guo‐Rong Xu, Liu‐Qing Xu, Zhi‐Fei Fu, Dan Xu, Wen‐Feng Chen, Chun‐Yan Cao, Yan Shi, Yi‐Heng Zeng, Jing Zhang, Xiao‐Chun Chen, Ru‐Xu Zhang, Ning Wang, Marina Kennerson, Dong‐Sheng Fan, Wan‐Jin Chen
Publikováno v:
Annals of neurologyReferences.
Despite the increasing number of genes associated with Charcot-Marie-Tooth (CMT) disease, many patients currently still lack appropriate genetic diagnosis for this disease. Autosomal dominant mutations in aminoacyl-tRNA synthetases (ARSs) have been i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a94aaebeb3fb265fbe72b211e64e423
https://pubmed.ncbi.nlm.nih.gov/36088542
https://pubmed.ncbi.nlm.nih.gov/36088542