Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Dan-ning Lou"'
Autor:
Zheng-Xiang Hu, Xiao-Dong Lu, Dan-Ning Lou, Meng-Lu Zhou, Qian-Ru Zhu, Shan-Shan Luo, Mei-Yuan Chen
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 1, Iss , Pp 72-73 (2019)
Externí odkaz:
https://doaj.org/article/ba5d796e57ab438ea049aeedbe85377d
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 77
To explore the influence of serum lactate dehydrogenase (LDH) level on remote diffusion-weighted imaging lesions (rDWILs) after spontaneous intracerebral hemorrhage (ICH). A consecutive cohort of 160 patients with spontaneous ICH who had brain MRI wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a75fd3d0509186c9daffd4333ebc932
https://pubmed.ncbi.nlm.nih.gov/32418810
https://pubmed.ncbi.nlm.nih.gov/32418810
Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family
Autor:
Jianfeng Xiao, Dan ning Lou, Zhi yuan Ouyang, Jin Cao, Ling Liu, Zhidong Cen, Dan Li, Zhong jin Wang, Fei Xie, Xing jiao Lu, Wei Luo, Hou min Yin
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 168:595-599
Familial cortical myoclonic tremor with epilepsy (FCMTE) is an autosomal dominant epilepsy syndrome. Four loci, including 8q24 (FCMTE1), 2p11.1-q12.2 (FCMTE2), 5p15.31-p15.1 (FCMTE3), and 3q26.32-3q28 (FCMTE4) were previously reported. Herein, we rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3c672fdb12c027053ae80166e3bd0f0
https://doi.org/10.1002/ajmg.b.32337
https://doi.org/10.1002/ajmg.b.32337
Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family
Autor:
Zhi-Dong, Cen, Fei, Xie, Dan-Ning, Lou, Xing-Jiao, Lu, Zhi-Yuan, Ouyang, Ling, Liu, Jin, Cao, Dan, Li, Hou-Min, Yin, Zhong-Jin, Wang, Jian-Feng, Xiao, Wei, Luo
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 168(7)
Familial cortical myoclonic tremor with epilepsy (FCMTE) is an autosomal dominant epilepsy syndrome. Four loci, including 8q24 (FCMTE1), 2p11.1-q12.2 (FCMTE2), 5p15.31-p15.1 (FCMTE3), and 3q26.32-3q28 (FCMTE4) were previously reported. Herein, we rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::581fa1a48e7c06f92a22cf188e6d778b
https://pubmed.ncbi.nlm.nih.gov/26130016
https://pubmed.ncbi.nlm.nih.gov/26130016