Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Qianyun Cai"'
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Spinal muscular atrophy (SMA) is an autosomal recessive disease caused by mutations in the survival motor neuron 1 (SMN1) gene on chromosome 5, leading to the degeneration of lower motor neurons. There are few studies on cognitive impairment comorbid
Externí odkaz:
https://doaj.org/article/5d3acf24f2d24766a83e8b962b6e959d
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:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background As sequencing technology has advanced in recent years, a series of synapse-related gene variants have been reported to be associated with autism spectrum disorders (ASDs). The α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid
Externí odkaz:
https://doaj.org/article/df286af76ac345ff9018ffb66e6dca48
Autor:
Xin Tong, Qianyun Cai, Dezhi Cao, Lifei Yu, Dan Sun, Guang Yang, Jiwen Wang, Hua Li, Zengning Li, Juan Wang, Shaoping Huang, Meiping Ding, Fang Fang, Qun Wang, Rong Luo, Jianxiang Liao, Jiong Qin
Publikováno v:
Acta Epileptologica, Vol 4, Iss 1, Pp 1-11 (2022)
Abstract Super-refractory status epilepticus (SRSE) is a serious and life-threatening neurological condition. Ketogenic diet (KD) is a diet characterized by high fat, low carbohydrate, and moderate protein. As KD shows effectiveness in controlling se
Externí odkaz:
https://doaj.org/article/cd9b44d6181c4e1093bd900b14ec0aaa
Publikováno v:
Chinese Medical Journal, Vol 128, Iss 1, Pp 128-130 (2015)
Externí odkaz:
https://doaj.org/article/839616e1d3594313ad510d8fca3228f7
Publikováno v:
Seizure. 99:75-81
Ketogenic diet (KD) is a well-established nonpharmacologic treatment for drug-resistant epilepsy. However, although KD has a long history of clinical use, there are still many difficulties with its real-world practice. This study retrospectively desc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eb558696c5a6884cbc7ec24f1b5af79
https://doi.org/10.1016/j.seizure.2022.04.015
https://doi.org/10.1016/j.seizure.2022.04.015
Background: Spinal muscular atrophy (SMA) is an autosomal recessive inherited disease. It is caused by mutations in the survival motor neuron1 (SMN1) gene on chromosome 5. The degeneration of lower motor neurons is the main feature. Current research
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d873326fa3db4bd181e11bc75a1ddd84
https://doi.org/10.21203/rs.3.rs-2880502/v1
https://doi.org/10.21203/rs.3.rs-2880502/v1
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
Autor:
Shenrong Zhong, Qianyun Cai, Longhe Zhong, Yuegang Wang, Fengchu Liang, Zhe Deng, Shasha Li, Daogang Zha, Weibao Qiu, Juefei Wu
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in MedicineReferences.
This study aims to determine the effect of low-intensity focused ultrasound (LIFU) in ischemic heart failure (IHF) and explore the potential neuroimmune mechanism.Sprague-Dawley rats were subjected to ultrasound (US) with specific parameters, and ele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acbd2024b7bd7c958a675c18a228bc80
https://pubmed.ncbi.nlm.nih.gov/36444908
https://pubmed.ncbi.nlm.nih.gov/36444908
We present a case of immunocompetent boy with brain abscess (BA) complicating hemophagocytic lymphohistiocytosis (HLH) and Kawasaki disease (KD), which is rarely reported. During the recovery period of BA, he had another fever accompanied by enlarged
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5bbacc3d3facff4e53ac336188c5e56
https://doi.org/10.22541/au.164873508.85315158/v1
https://doi.org/10.22541/au.164873508.85315158/v1