Zobrazeno 1 - 8
of 8
pro vyhledávání: '"De-Kang Gan"'
Autor:
Yu-He Qi, Feng-Juan Gao, Fang-Yuan Hu, Sheng-Hai Zhang, Jun-Yi Chen, Wan-Jing Huang, Guo-Hong Tian, Min Wang, De-Kang Gan, Ji-Hong Wu, Ge-Zhi Xu
Publikováno v:
Frontiers in Genetics, Vol 8 (2017)
Purpose: To show early, rapid and accurate molecular diagnosis of occult macular dystrophy (OMD) in a four-generation Chinese family with inherited macular dystrophy.Methods: In the current study, we comprehensively screened 130 genes involved in com
Externí odkaz:
https://doaj.org/article/798561fa7f70406ebf862fa7e3ab56ad
Publikováno v:
International Journal of Ophthalmology, Vol 7, Iss 1, Pp 169-172 (2014)
AIM: To identify the mutations in RS1 gene associated with typical phenotype of X-linked juvenile retinoschisis (XLRS) and a rare condition of concomitant glaucoma.METHODS: Complete ophthalmic examinations were performed in the proband. The coding re
Externí odkaz:
https://doaj.org/article/0196c1c22dbd4206945e1e0a241b596f
Publikováno v:
Neuroscience Letters. 500:16-19
X-linked retinitis pigmentosa (XLRP) is the most severe type of retinitis pigmentosa (RP), with patients consistently showing early onset and rapid deterioration. Obtaining a genetic diagnosis for a family with XLRP is important for counseling purpos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d00c79ec16be0e594486fae740c0ee5f
https://doi.org/10.1016/j.neulet.2011.05.234
https://doi.org/10.1016/j.neulet.2011.05.234
Publikováno v:
Experimental neurology. 219(2)
Direct electrical stimulation of neural tissues is a strategic approach to treat injured axons by accelerating their outgrowth [Al-Majed, A.A., Neumann, C.M., Brushart, T.M., Gordon, T., 2000. Brief electrical stimulation promotes the speed and accur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e925aeeae4104668b6bbd223e0ca875d
https://pubmed.ncbi.nlm.nih.gov/19576889
https://pubmed.ncbi.nlm.nih.gov/19576889
Publikováno v:
Retina (Philadelphia, Pa.). 28(4)
To investigate macular hole (MH) formation in patients with retinitis pigmentosa (RP) and to determine surgical prognosis for these patients.Data for four RP patients with MHs were retrospectively reviewed. Comprehensive ocular examinations, includin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c96a4c6c1744c4df2e236459e4333801
https://pubmed.ncbi.nlm.nih.gov/18398364
https://pubmed.ncbi.nlm.nih.gov/18398364
Publikováno v:
Experimental Neurology. 220:410-411
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63b7ded4b4305ae459bf188a8ba08c99
https://doi.org/10.1016/j.expneurol.2009.09.018
https://doi.org/10.1016/j.expneurol.2009.09.018
Autor:
Fen-Fen Li, Xiu-Feng Huang, Jie Chen, Xu-Dong Yu, Mei-Qin Zheng, Fan Lu, Zi-Bing Jin, De-Kang Gan, Li, Fen-Fen, Huang, Xiu-Feng, Chen, Jie, Yu, Xu-Dong, Zheng, Mei-Qin, Lu, Fan, Jin, Zi-Bing, Gan, De-Kang
Publikováno v:
Journal of Translational Medicine; 10/22/2015, Vol. 13, p1-8, 8p
Autor:
Fen‑Fen Li, Zi-Bing Jin, Mei‑Qin Zheng, Jie Chen, Xiu-Feng Huang, De‑Kang Gan, Xu‑Dong Yu, Fan Lu
Publikováno v:
Journal of Translational Medicine
Background Achromatopsia (ACHM) is a severe congenital autosomal recessive retinal disorder caused by loss of cone photoreceptors. Here, we aimed to determine the underlying genetic lesions and phenotypic correlations in two Chinese families with ACH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2ca4f6582fc326576c1825190ea19f3