Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Junlan Lv"'
Autor:
Xihua Li, Junlan Lv, Wenhua Zhu, Siqi Hong, Zhiqiang Wang, Xingzhi Chang, Ying Xu Gao, Yangmei Zhou, Caiping Jia, Jia Fang, Terrell A. Patterson
Publikováno v:
The Lancet Regional Health. Western Pacific, Vol 42, Iss , Pp 100944- (2024)
Summary: Background: Duchenne muscular dystrophy (DMD) is a disabling and life-threatening, X-linked recessive disorder caused by mutations in dystrophin. Natural history studies can inform the disease characteristics of DMD, and data from these stud
Externí odkaz:
https://doaj.org/article/8c5a4151318c4a178a77e3922934f78e
Autor:
Junlan Lv, Getu Zhaori
Publikováno v:
Pediatric Investigation, Vol 6, Iss 1, Pp 1-4 (2022)
Externí odkaz:
https://doaj.org/article/f08dc25756e84868bf97b54cc78182d6
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Although SCN1A variants result in a wide range of phenotypes, genotype-phenotype associations are not well established. We aimed to explore the phenotypic characteristics of SCN1A associated seizure diseases and establish genotype-phenotype correlati
Externí odkaz:
https://doaj.org/article/74cb536fbd694f04a98b276c72c66063
Autor:
Xiaohui Wang, Changhong Ding, C H Chen, Changhong Ren, Fang Fang, Zhuo Xiuwei, Shuai Gong, Weihua Zhang, Hongzhi Guan, Xiaotun Ren, Xinying Yang, Jiuwei Li, Lifang Dai, Tongli Han, Haitao Ren, Weixing Feng, Junlan Lv, Shen Zhang, Ji Zhou
Publikováno v:
European Journal of Paediatric Neurology. 34:67-73
Objective To describe the clinical features and prognosis of pediatric anti-N-methyl- d -aspartate receptor (NMDAR) encephalitis from a single center in northern China. Methods The clinical and laboratory characteristics of hospitalized patients with
Autor:
Junling Wang, Minako Ogawa-Tominaga, Jianing Wang, Weihua Zhang, Fang Fang, Xiaohui Wang, Kei Murayama, Victor Wei Zhang, Masaru Shimura, Li Zhang, Wei Shi, Junlan Lv, Zhimei Liu
Publikováno v:
Mitochondrion. 57:222-229
Childhood-onset dystonia with optic atrophy and basal ganglia abnormalities is an extremely rare autosomal recessive mitochondrial disease caused by biallelic mutations in MECR. Using whole-exome sequencing, we identified a novel homozygous MECR muta
Autor:
Rui Ban, Robert Kopajtich, Junlan Lv, Sarah L Stenton, Masaru Shimura, Zhaoxia Wang, Yun Yuan, Junling Wang, Xiaodi Han, Zhimei Liu, Qiang Shi, Chuanqiang Pu, Holger Prokisch, Fang Fang, Matthias Elstner
Publikováno v:
Brain 145, e125-e127 (2022)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a5319d070c4b0b5f12f7040b0853af8
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=66387
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=66387
Publikováno v:
Frontiers in molecular neuroscience. 15
Although
Autor:
Junlan Lv, Hua Wang, Dong Wang, Zhong-Dong Lin, Jiong Qin, Yi Wang, Rong Luo, Yu-Qin Zhang, Yin-Bo Chen, Sui-Qiang Zhu
Publikováno v:
World Journal of Pediatrics. 13:551-559
To assess efficacy and safety of oxcarbazepine (OXC) oral suspension in pediatric patients aged 2–16 years with partial seizures (PS) and/or generalized tonic-clonic seizures (GTCS) in real-world clinical practice in China. This 26-week, single arm
Autor:
Tongli Han, Zhimei Liu, Shufang Li, Hezhi Fang, Ying Shen, Yun Wu, Suzhen Sun, Danmin Shen, Changhong Ding, Jianxin Lv, Fang Fang, Lei Yang, Junlan Lv, Jian Wu
Publikováno v:
Science China Life Sciences. 60:746-757
Mitochondrial disease was a clinically and genetically heterogeneous group of diseases, thus the diagnosis was very difficult to clinicians. Our objective was to analyze clinical and genetic characteristics of children with mitochondrial disease in C
Publikováno v:
Applied Organometallic Chemistry. 33