Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Qiuji Tao"'
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background Spinal muscular atrophy (SMA) is a progressive degenerative neuromuscular disease. Nusinersen, with its quick onset of action, can benefit patients early in the treatment course. However, there are currently no clinical studies re
Externí odkaz:
https://doaj.org/article/078676685fa74d70a9e076048f017ebe
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Background and purposeA growing body of research suggests that inflammation and maternal infections may lead to an increased risk of neurodevelopmental problems such as attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD),
Externí odkaz:
https://doaj.org/article/0c24203f107c433d9e6d64bd70beb0b1
Autor:
Jun Chen, Qiuji Tao, Lijuan Fan, Yajun Shen, Jinfeng Liu, Huan Luo, Zuozhen Yang, Mengmeng Liang, Jing Gan
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 10, Pp n/a-n/a (2022)
Abstract Background Typical patients with KCNQ2 (OMIM# 602235) epileptic encephalopathy present early neonatal‐onset intractable seizures with a burst suppression EEG pattern and severe developmental delay or regression, and those patients always f
Externí odkaz:
https://doaj.org/article/4f44b533db1d4d0eacf3488c2e662e63
Introduction: The treatment of children with spinal muscular atrophy (SMA) includes disease-modifying drugs such as nusinersen. Our aim was to summarize our experience regarding the efficacy and safety of nusinersen and nutritional status in children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::953a56ee6211957f5c5da8df732ce42f
https://doi.org/10.21203/rs.3.rs-1914460/v1
https://doi.org/10.21203/rs.3.rs-1914460/v1
Publikováno v:
Psychiatry and Clinical Neurosciences. 76:58-59