Zobrazeno 1 - 10
of 827
pro vyhledávání: '"Xue, Ma"'
Publikováno v:
BMC Infectious Diseases, Vol 24, Iss 1, Pp 1-5 (2024)
Abstract Cryptococcal infection of central nervous system commonly involves meningitis or meningoencephalitis, but rarely mimics inflammatory myelitis. We present short segment myelitis as a dominant manifestation caused by Cryptococcus neoformans in
Externí odkaz:
https://doaj.org/article/390c00e01790418f9f6ec67d18e123af
Autor:
Qiyu Dong, Xiaojie Yin, Shuanglong Fan, Sheng Zhong, Wenxin Yang, Keer Chen, Qian Wang, Xue Ma, Refiloe Laurentinah Mahlatsi, Yanling Yang, Jianxin Lyu, Hezhi Fang, Ya Wang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Leigh syndrome (LS) is a common mitochondrial disease caused by mutations in both mitochondrial and nuclear genes. Isoleucyl-tRNA synthetase 2 (IARS2) encodes mitochondrial isoleucine-tRNA synthetase, and variants in IARS2 have be
Externí odkaz:
https://doaj.org/article/e0dc0c332a5b4c46a0d697210083b4e3
Autor:
Hui Dong, Tian Sang, Xue Ma, Jinqing Song, Zhehui Chen, Huiting Zhang, Ying Jin, Mengqiu Li, Dingding Dong, Liying Sun, Zhijun Zhu, Yao Zhang, Yanling Yang
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Carbamoyl phosphate synthetase 1 (CPS1) deficiency (OMIM 237300), an autosomal recessive rare and severe urea cycle disorder, is associated with hyperammonemia and high mortality. Methods Herein we present 12 genetic variants iden
Externí odkaz:
https://doaj.org/article/7dd632f2570f4229af3d9a3266716381
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-3 (2024)
Abstract Background Urachal carcinoma is an extremely rare malignant tumor originating from the urachus. Urachal adenocarcinoma has never been reported in patients under 20 years of age. In this case, we describe a 15-year-old patient with urachal ad
Externí odkaz:
https://doaj.org/article/d41f5caa5a054aa3888b3ebd8c39db0e
Autor:
Hui Dong, Xue Ma, Zhehui Chen, Huiting Zhang, Jinqing Song, Ying Jin, Mengqiu Li, Mei Lu, Ruxuan He, Yao Zhang, Yanling Yang
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background and aims To investigate the clinical features, ALDH5A1 gene variations, treatment, and prognosis of patients with succinic semialdehyde dehydrogenase (SSADH) deficiency. Materials and methods This retrospective study evaluated the
Externí odkaz:
https://doaj.org/article/846d3e94ce754f93a905fef29068c85b
Publikováno v:
Plant Protection Science, Vol 60, Iss 2, Pp 172-180 (2024)
This study aimed to examine the antifungal effects of nine monoterpenes on Sclerotinia sclerotiorum via the mycelial growth rate method. The effects of carvacrol on the morphological structures of hyphae were investigated by scanning electron microsc
Externí odkaz:
https://doaj.org/article/28e7c7a679e94efdb3de5f9d791d6dba
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-11 (2024)
Abstract Endowing the widely-used synthetic polymer nylon with high-performance organic room-temperature phosphorescence would produce advanced materials with a great potential for applications in daily life and industry. One key to achieving this go
Externí odkaz:
https://doaj.org/article/ce446ba693074b7ea4962e8a5e60400d
Publikováno v:
Results in Physics, Vol 63, Iss , Pp 107870- (2024)
Piezoelectric energy harvesting of mechanical waves exhibits great potential applications in electricity generation for low-powered electronic devices. In this work, the metasurface-assisted phononic cavity is proposed for the enhancement of piezoele
Externí odkaz:
https://doaj.org/article/756032173a9b46b4ace6f50c6f9c84bb
Autor:
Yupeng Liu, Xue Ma, Zhehui Chen, Ruxuan He, Yao Zhang, Hui Dong, Yanyan Ma, Tongfei Wu, Qiao Wang, Yuan Ding, Xiyuan Li, Dongxiao Li, Jinqing Song, Mengqiu Li, Ying Jin, Jiong Qin, Yanling Yang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-6 (2024)
Abstract Background Clinicians traditionally aim to identify a singular explanation for the clinical presentation of a patient; however, in some cases, the diagnosis may remain elusive or fail to comprehensively explain the clinical findings. In rece
Externí odkaz:
https://doaj.org/article/2660592616f1486c9a1b8a5ce6020c5b
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundNeuromyelitis optica spectrum disorder (NMOSD) is an inflammatory autoimmune disease affecting the central nervous system (CNS). NMOSD pathogenesis involves systemic inflammation. However, a causal relationship between circulating cytokine
Externí odkaz:
https://doaj.org/article/67cffd9814c849f19387b01371c4f0a0