Zobrazeno 1 - 10
of 6 773
pro vyhledávání: '"Wilson′s Disease"'
Publikováno v:
Journal of Inflammation Research, Vol Volume 17, Pp 9601-9616 (2024)
Hong Chen,* Xie Wang,* Nian Peng, Yue Pu, Hao Ye, Yu Gui, Rui Zhang, Juan Zhang Department of Neurology, The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hefei, 230031, People’s Republic of China*These
Externí odkaz:
https://doaj.org/article/cf156884462f42f4acde22ec85056bf3
Publikováno v:
Case Reports in Ophthalmology, Vol 15, Iss 1, Pp 724-728 (2024)
Introduction: Wilson’s disease is a rare autosomal recessive disorder that disrupts copper metabolism. It presents with distinctive ocular manifestations. Oculodermal melanosis, commonly referred to as nevus of Ota, is a painless condition characte
Externí odkaz:
https://doaj.org/article/54e6880714bc403087c43713913ce0c2
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract According to early research, the incidence of claustrum lesions in patients with neurological Wilson’s disease (WD) was inconsistent, ranging from 1.8 to 75% on magnetic resonance imaging (MRI). Our study aims to explore the incidence, cli
Externí odkaz:
https://doaj.org/article/b4d7a896591b45b9b83ca5be14f315f1
Autor:
Jianjian Dong, Guanghai Xiang, Xiaoxue Xia, Lewen Xu, Peihua Wen, Chenchen Xu, Yin Xu, Yushuang Su, Yanze Song, Haiyang Tong, Qingjun Zhu, Yongzhu Han, Yongsheng Han, Nan Cheng, Haoyi Wang, Hong Zhou
Publikováno v:
Journal of Neuroinflammation, Vol 21, Iss 1, Pp 1-17 (2024)
Abstract Pathogenic germline mutations in the P-type copper-transporting ATPase (ATP7B) gene cause Wilson’s disease (WD), a hereditary disorder characterized by disrupted copper metabolism. The Arg778Leu (R778L) mutation in exon 8 is prevalent amon
Externí odkaz:
https://doaj.org/article/15332235f7c74a60be8f626d891f037c
Publikováno v:
International Medical Case Reports Journal, Vol Volume 17, Pp 819-822 (2024)
Nuri Mehmet Basan,1 Mohamed Sheikh Hassan,2 Zeynep Gökhan,1 Sena Nur Alper,1 Sümeyye Şevval Yaşar,1 Tuğçe Gür,1 Ayhan Köksal1 1Department of Neurology, University of Health Science, Başakşehir Çam and Sakura C
Externí odkaz:
https://doaj.org/article/e1dcf06b9ac44cc69a471dc00f9d89dd
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Hepatolenticular degeneration (HLD), also known as Wilson's disease (WD), is a rare autosomal recessive disorder regarding copper metabolism. Whether gut microbiota imbalance is involved in developing HLD remains unknown. A comprehensive 16S
Externí odkaz:
https://doaj.org/article/f2201495b7de446ba653d29af30fc2f2
Publikováno v:
Journal of Inflammation Research, Vol Volume 17, Pp 5599-5618 (2024)
Yuya Wen,1 Chenling Zhao,1 Jie Chen,1 Liwei Tian,1 Bojin Wu,1 Wenting Xie,1 Ting Dong1,2 1Department of Neurology, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, 230031, People’s Republic of China; 2Key Laboratory of
Externí odkaz:
https://doaj.org/article/06fab4be0d2440e28d6d3a383b800a4f
Case series on neuroimaging spectrum of Wilson’s disease: knowing the known and the uncommonly known
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 55, Iss 1, Pp 1-8 (2024)
Abstract Background Wilson’s disease is an inherited disease characterized by impaired copper metabolism that causes damage to many organs, including the brain. Patients having neurological involvement usually present with varied neuropsychiatric s
Externí odkaz:
https://doaj.org/article/543cb89daa654d96834fddcf7015c4b3
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
Synaptic efficacy is critical for memory formation and consolidation. Accumulating evidence suggest that synapses are impaired during Wilson’s disease (WD), contributing to neuronal dysfunction and cognitive decline. WD is a prototypical condition
Externí odkaz:
https://doaj.org/article/20579407d592477f8e494a122e380770
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
ObjectiveThis study aims to analyze the lipid metabolism patterns and identify risk factors for dyslipidemia in Wilson’s Disease (WD), offering novel insights into diagnosis and treatment strategies for unexplained dyslipidemia.MethodsData from Wil
Externí odkaz:
https://doaj.org/article/4533108bc87346ec898cafec7c4234c8