Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ling-Chao MENG"'
Autor:
Hao-quan WANG, Wei-min DAI, Zi-xu ZHANG, Meng-shuo LI, Ling-chao MENG, Zheng ZHANG, Huan LU, Xiao-ling SONG, Sheng QIANG
Publikováno v:
Journal of Integrative Agriculture, Vol 22, Iss 1, Pp 149-169 (2023)
Rice, the main food crop in China, has been sporadically reported to suffer from weedy rice infestation. However, the overall occurrence and distribution pattern of Chinese weedy rice remains unclear because a systematic survey has not been conducted
Externí odkaz:
https://doaj.org/article/5515d833a3094c0fb8ecbd3c1f4ca059
Autor:
Yan-Yan Xue, Hao-Ling Cheng, Hai-Lin Dong, Hou-Min Yin, Yun Yuan, Ling-Chao Meng, Zhi-Ying Wu, Hao Yu
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Charcot-Marie-Tooth (CMT) disease is a group of inherited peripheral neuropathies, which are subdivided into demyelinating and axonal forms. Biallelic mutations in POLR3B are the well-established cause of hypomyelinating leukodyst
Externí odkaz:
https://doaj.org/article/4d3ac404a0f84e209fcda2b393229cf9
Clinical features of autoimmune autonomic neuropathy with onset of acute autonomic nerve dysfunction
Autor:
Fan LI, Ling⁃chao MENG, Jing BAI, Yun⁃chuang SUN, Ru⁃jie LI, Xin SHI, Hong⁃jun HAO, Feng GAO, Zhi⁃rong JIA, Yi⁃ning HUANG, Yun YUAN, Zhao⁃xia WANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 20, Iss 10, Pp 868-876 (2020)
Background Autoimmune autonomic neuropathy with onset of acute autonomic nerve dysfunction is often misdiagnosed because its main symptoms are syncope and gastrointestinal motility disorder. This study summarized the clinical, electrophysiological an
Externí odkaz:
https://doaj.org/article/6972d59048ca4bcba1fe8ba64bc078f8
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 19, Iss 6, Pp 405-410 (2019)
Objective To investigate the clinical and neuropathological features of N-hexane toxic peripheral neuropathy which was misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Methods and Results Two patients presented with s
Externí odkaz:
https://doaj.org/article/2260b16206b449b2afa94ee3be6868f0
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 16, Iss 10, Pp 689-695 (2016)
Objective To investigate the clinical manifestations and auxiliary examination features of necrotizing autoimmune myopathy (NAM). Methods According to the inclusion criteria from European Neuromuscular Center (ENMC) International Workshop on idiopath
Externí odkaz:
https://doaj.org/article/b4a4b2db5e654e60b0c2b52682282065
Publikováno v:
Chinese Medical Journal, Vol 128, Iss 21, Pp 2902-2905 (2015)
Background: Mutations of transthyretin (TTR) cause the most common type of autosomal-dominant hereditary systemic amyloidosis, which occurs worldwide. To date, more and more mutations in the TTR gene have been reported. Some variations in the clinica
Externí odkaz:
https://doaj.org/article/cca81e3d1c1f488b8931bb2f15288fb8
Publikováno v:
Land Degradation & Development. 33:3163-3173
Publikováno v:
Medical Journal of Chinese People's Liberation Army, Vol 46, Iss 2, Pp 114-121 (2021)
Objective To investigate the gender difference of cognitive function in neonatal rats treated with sevoflurane. Methods Eighty two postnatal 7-day (P7) SD rats were randomly divided into control group and sevoflurane treated group, then divided into
Autor:
Ling-Chao MENG, Meng-Meng LI, Cheng-Qi DENG, Xiao-Yan FANG, Jian WU, Yi-Qing HAO, Wei-Wei LIU, Wen-Feng LI
Publikováno v:
Medical Journal of Chinese People's Liberation Army, Vol 45, Iss 4, Pp 416-422 (2020)
Objective To retrospectively analyze the effects of anesthesia mode on the perioperative period and postoperative outcome in patients with traumatic fractures. Methods A total of 699 patients with traumatic shoulder fractures and hip fractures, admit
Autor:
Hao-Ling Cheng, Hai-Lin Dong, Zhi-Ying Wu, Ling-Chao Meng, Hou-Min Yin, Yan-Yan Xue, Yun Yuan, Hao Yu
Publikováno v:
BMC Neurology
BMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)
BMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)
Background Charcot-Marie-Tooth (CMT) disease is a group of inherited peripheral neuropathies, which are subdivided into demyelinating and axonal forms. Biallelic mutations in POLR3B are the well-established cause of hypomyelinating leukodystrophy, wh