Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Xiuwei, Zhuo"'
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-9 (2024)
Abstract Background To understand the clinical characteristics and prognosis of respiratory syncytial virus (RSV)-related encephalopathy in children. Methods A retrospective analysis of the data of children who were diagnosed with RSV-related encepha
Externí odkaz:
https://doaj.org/article/86125e7ea0f6489c9e811b4a2f9d6255
Publikováno v:
Pediatric Investigation, Vol 6, Iss 3, Pp 219-223 (2022)
ABSTRACT Introduction Pathogenic variants in PLOD3, encoding lysyl hydroxylase‐3 (LH3), can cause a hereditary connective tissue disorder that has rarely been reported. It is a multi‐system disease, presenting with craniofacial dysmorphisms, skel
Externí odkaz:
https://doaj.org/article/17d6b48241ed41e2ab572c45ffca446b
Publikováno v:
Pediatric Investigation, Vol 6, Iss 2, Pp 140-143 (2022)
ABSTRACT Introduction Primary angiitis of the central nervous system (PACNS) is a vasculitis confined to the CNS. A small proportion of the lesions may present as a tumor‐like mass, which is rarely seen in children. Case presentation A 5‐year‐o
Externí odkaz:
https://doaj.org/article/d08eea399f654cb980f454b2d7d9d972
Autor:
Weihua Zhang, Jiuwei Li, Xiuwei Zhuo, Ji Zhou, Weixing Feng, Shuai Gong, Xiaotun Ren, Changhong Ding, Tongli Han, Fang Fang
Publikováno v:
Pediatric Investigation, Vol 6, Iss 1, Pp 5-10 (2022)
ABSTRACT Importance The phenotypes of ATP1A3 gene mutations are diverse. Relapsing encephalopathy with cerebellar ataxia and fever‐induced paroxysmal weakness and encephalopathy (FIPWE) are considered non‐classical phenotypes caused by p.Arg756 m
Externí odkaz:
https://doaj.org/article/e5844d634c474755b736bae995ce32e6
Autor:
Zhang, Weihua, Ren, Changhong, Wang, Xiaohui, Li, Jiuwei, Ding, Changhong, Han, Tongli, Lv, Junlan, Chen, Chunhong, Gong, Shuai, Xiuwei, Zhuo, Dai, Lifang, Feng, Weixing, Yang, Xinying, Zhang, Shen, Zhou, Ji, Ren, Haitao, Guan, Hongzhi, Ren, Xiaotun, Fang, Fang
Publikováno v:
In European Journal of Paediatric Neurology September 2021 34:67-73
Autor:
Ji Zhou, Mei Jin, Yan Su, Xiuwei Zhuo, Libing Fu, Xiaotun Ren, Changhong Ren, Zhou, Anna, Jiuwei Li, Weihua Zhang
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation; May2024, Vol. 11 Issue 3, p1-9, 9p
Autor:
Xiaoting Lou, Yuwei Zhou, Zhimei Liu, Yaojun Xie, Luyi Zhang, Suzhou Zhao, Shuai Gong, Xiuwei Zhuo, Junling Wang, Lifang Dai, Xiaotun Ren, Xiao Tong, Liangliang Jiang, Hezhi Fang, Fang Fang, Jianxin Lyu
Publikováno v:
Gene. 860:147229
Autor:
Ji Zhou, Jiuwei Li, Changhong Ren, Anna Zhou, Xiuwei Zhuo, Shuai Gong, Changhong Ding, Fang Fang, Weihua Zhang, Xiaotun Ren
Publikováno v:
Multiple sclerosis and related disorders. 68
To evaluate the efficacy of mycophenolate mofetil (MMF) in the treatment of childhood MOG-IgG-associated disorder (MOGAD).Thirty patients diagnosed with relapsing MOGAD and treated with MMF for1 year from a childhood MOGAD ambispective cohort were in
Autor:
Weihua, Zhang, Jiuwei, Li, Xiuwei, Zhuo, Ji, Zhou, Weixing, Feng, Shuai, Gong, Xiaotun, Ren, Changhong, Ding, Tongli, Han, Fang, Fang
Publikováno v:
Pediatric investigation. 6(1)
The phenotypes ofTo summarize the clinical manifestations, treatment, and follow-up of Chinese patients with p.Arg756 mutations ofWe analyzed the clinical features, treatment, and genotypes of eight children with p.Arg756 mutations ofEight patients (