Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Xiaotang Cai"'
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundStudies have found maternal smoking during pregnancy was linked to attention-deficit/hyperactivity disorder (ADHD) risk. It is unclear if maternal smoking cessation during pregnancy lowers ADHD and learning disability (LD) risk in offspring
Externí odkaz:
https://doaj.org/article/98fd1ef1b4ed4f778dbdb6707f509f58
Autor:
Lekai Luo, Yi Liao, Fenglin Jia, Gang Ning, Jing Liu, Xuesheng Li, Xijian Chen, Xinmao Ma, Xuejia He, Chuan Fu, Xiaotang Cai, Haibo Qu
Publikováno v:
Translational Psychiatry, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Tourette syndrome (TS) is a developmental neuropsychiatric disorder characterized by repetitive, stereotyped, involuntary tics, the neurological basis of which remains unclear. Although traditional resting-state MRI (rfMRI) studies have iden
Externí odkaz:
https://doaj.org/article/7eb4117ddf184900ae71eaa14440167c
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-11 (2023)
Abstract Background Duchenne muscular dystrophy (DMD) is a fatal genetic muscle-wasting disease that affects 1 in 5000 male births with no current cure. Despite great progress has been made in the research of DMD, its underlying pathological mechanis
Externí odkaz:
https://doaj.org/article/75cbebd186504dcfa64bdd2f731fbf19
Autor:
Yaru Cui, Shuran Shao, Linling Zhang, Liting Tang, Peihuan Xie, Li Wei, Hongyu Duan, Yimin Hua, Xiaotang Cai, Kaiyu Zhou, Chuan Wang
Publikováno v:
Reviews in Cardiovascular Medicine, Vol 25, Iss 8, p 309 (2024)
Background: The prognosis of Duchenne muscular dystrophy (DMD) is poor once it develops to the stage of cardiac impairment. Recent studies have demonstrated that electrocardiogram (ECG), which consists of general ECG and vectorcardiogram (VCG), retai
Externí odkaz:
https://doaj.org/article/380782b48c8143888af76b11a549e4a6
Autor:
Jieni Jiang, Xiaotang Cai, Haibo Qu, Qiang Yao, Tiantian He, Mei Yang, Hui Zhou, Xuemei Zhang
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
ObjectiveFacioscapulohumeral muscular dystrophy type 1 (FSHD1) is one of the most common forms of autosomal-dominant muscular dystrophies characterized by variable disease penetrance due to shortened D4Z4 repeat units on 4q35. The molecular diagnosis
Externí odkaz:
https://doaj.org/article/9c8cd440307a4edfae57a7c9a20289ba
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare inherited cerebral white matter disorder in children. Pathogenic variations in the causative gene MLC1 are found in approximately 76% of patients and are inherited in an autos
Externí odkaz:
https://doaj.org/article/715833ed0bf3412988db6178609edec5
Autor:
Tiantian He, Huaqin Sun, Bocheng Xu, Haibo Qu, Xiaotang Cai, Hui Zhou, Yanyan Liu, Ziyuan Lin, Xuemei Zhang
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Pontocerebellar hypoplasia type 8(PCH8) is a rare neurodegenerative disorder, reportedly caused by pathogenic variants of the CHMP1A in autosomal recessive inheritance, and CHMP1A variants have also been implicated in other diseases, and yet none of
Externí odkaz:
https://doaj.org/article/6b8dc3345d7d4d619b9b714c8b53ce00
Autor:
Rong Xu, Huayan Xu, Kun Zhang, Hong Xu, Hui Liu, Hang Fu, Linjun Xie, Ke Xu, Chuan Fu, Xuesheng Li, Xiaoyue Zhou, Rajiv Ananthakrishna, Joseph B. Selvanayagam, Li Yu, Xiaotang Cai, Yingkun Guo, Yanjie Yin
Publikováno v:
Chinese Medical Journal, Vol 136, Iss 9, Pp 1132-1134 (2023)
Externí odkaz:
https://doaj.org/article/bdbb093609274672a4a9b0e1f6cdda01
Publikováno v:
BMC Musculoskeletal Disorders, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background Little is known about the disease distribution and severity detected by T1-mapping in Duchenne muscular dystrophy (DMD). Furthermore, the correlation between skeletal muscle T1-values and clinical assessments is less studied. Henc
Externí odkaz:
https://doaj.org/article/d24583578e3c4027a889febeebca26e1
Autor:
Yi Liao, Xiuli Li, Fenglin Jia, Yuexin Jiang, Gang Ning, Xuesheng Li, Chuan Fu, Hui Zhou, Xuejia He, Xiaotang Cai, Haibo Qu
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
Tourette syndrome (TS) is a neurodevelopment disorder characterized by motor and phonic tics. We investigated the topological alterations in pediatric TS using morphological topological analysis of brain structures. We obtained three-dimensional T1-w
Externí odkaz:
https://doaj.org/article/c7a1f7087e594ca3a56e8f68888f4be2