Zobrazeno 1 - 10
of 149
pro vyhledávání: '"An Guor Wang"'
Autor:
Tsai-Chu Yeh, Dau-Ming Niu, Hui-Chen Cheng, Yun-Ru Chen, Li-Zhen Chen, Shu-Ping Tsui, Ting-Wei Ernie Liao, An-Guor Wang, Chia-Feng Yang
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 33, Iss , Pp 100937- (2022)
A seven-month-old girl presented with bilateral roving nystagmus, hyperopia, and retinal dystrophy, and was brought to our ophthalmology clinic. Visual-evoked potentials (VEPs) were non-recordable in both the eyes. No other systemic symptoms or abnor
Externí odkaz:
https://doaj.org/article/d2250adafff4439281bc6965aebc7a85
Autor:
Nancy J Newman, Valérie Biousse, José-Alain Sahel, Patrick Yu-Wai-Man, Sean Donahue, Gema Rebolleda, Prem S Subramanian, Bart P Leroy, Alfredo A Sadun, Robert C Sergott, Catherine Vignal-Clermont, Bart K Chwalisz, Mark Moster, An-Guor Wang, Valerio Carelli, Rudrani Banik, Fabienne Bazin, Eric Cox, Michel Roux, Magali Taiel, Amore Giulia, Anand Shweta, Banik Rudrani, Barboni Piero, Biousse Valérie, Boston Hayley, Burale Asma, Carbonelli Michele, Carelli Valerio, Chen Celia, Cheng Hui-Chen, Cho Steve, K Chwalisz Bart, Contin Manuela, D’Agati Pietro, A DeBusk Adam, De Zaeytijd Julie, Dobbs Jannah, P Donahue Sean, DuBois Lindreth, Esposti Simona, Fernandes Filho Alcides, Fortin Elizabeth, Gangaputra Sapna, Gibbs Deborah, Girmens Jean François, Hage Rabih, A Haller Julia, Heilweil Gad, Hubbard III GeorgeBaker, Hwang Jeong-Min, Jaumendreu Urquijo Laia, Jurkute Neringa, Karanjia Rustum, Khemliche Wahiba, La Morgia Chiara, P Leroy Bart, Massini Maria, Mathias Marc, A Memon Muhammad, Mohamed Susan, L Moster Mark, J Muñoz NegreteFrancisco, J Newman Nancy, O’Keefe Ghazala, Patel Shriji, Pecen Paula, H Peragallo Jason, Plaine Lise, Preston Mary, Rebolleda Fernández Gema, Romagnoli Martina, A Sadun Alfredo, A Sahel José, SantaMaria Melissa, C Sergott Robert, S Subramanian Prem, Sun Chuanbin, Tai Katy, Tollis Heather, Tsui Irena, R Tucker William, Vignal-Clermont Catherine, Wang An-Guor, Wilkins Saige, Yu-Wai-Man Patrick
Publikováno v:
BMJ Open Ophthalmology, Vol 7, Iss 1 (2022)
Objective REFLECT is the first randomised, double-masked, placebo-controlled multicentre phase 3 clinical trial that evaluated the efficacy and safety of bilateral intravitreal (IVT) injection of lenadogene nolparvovec in subjects with Leber heredita
Externí odkaz:
https://doaj.org/article/c3ae820deb6448238032cfa7c2f4a8d2
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11891 (2022)
Leber’s hereditary optic neuropathy (LHON) is a maternally transmitted disease caused by mitochondria DNA (mtDNA) mutation. It is characterized by acute and subacute visual loss predominantly affecting young men. The mtDNA mutation is transmitted t
Externí odkaz:
https://doaj.org/article/c0311a37c3b840d9a8fd4e45bcd9604b
Publikováno v:
Biomedicines, Vol 10, Iss 8, p 1930 (2022)
Molecular pathophysiology of LHON was reviewed and the current status of gene therapy for LHON is updated.
Externí odkaz:
https://doaj.org/article/5ac0c325273a4373be31ca40f23e0ed0
Autor:
Yi-Ping Yang, Yuh-Lih Chang, Yun-Hsien Lai, Ping-Hsing Tsai, Yu-Jer Hsiao, Long Hoang Nguyen, Xue-Zhen Lim, Chang-Chi Weng, Yu-Ling Ko, Chang-Hao Yang, De-Kuang Hwang, Shih-Jen Chen, Shih-Hwa Chiou, Guang-Yuh Chiou, An-Guor Wang, Yueh Chien
Publikováno v:
Biomedicines, Vol 10, Iss 4, p 788 (2022)
Backgrounds: Leber’s hereditary optic neuropathy (LHON) is known as an inherited retinal disorder characterized by the bilateral central vision loss and degeneration of retinal ganglion cells (RGCs). Unaffected LHON carriers are generally asymptoma
Externí odkaz:
https://doaj.org/article/4ba1d2349b084ec2b50e2664a3f85da0
Autor:
Huai-En Lu, Yi-Ping Yang, Yan-Ting Chen, You-Ren Wu, Chia-Lin Wang, Fu-Ting Tsai, De-Kuang Hwang, Tai-Chi Lin, Shih-Jen Chen, An-Guor Wang, Patrick C.H. Hsieh, Shih-Hwa Chiou
Publikováno v:
Stem Cell Research, Vol 28, Iss , Pp 56-60 (2018)
Leber's hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease caused by homoplasmic point mutations in complex I subunit genes of mitochondrial DNA. In this report, we generated an induced pluripotent stem cell (iPSCs) li
Externí odkaz:
https://doaj.org/article/27f2e3f493304657a38a2d0a004a5c4f
Publikováno v:
Documenta Ophthalmologica. 145:263-270
To report the clinical features of a patient with melanoma-associated retinopathy (MAR) with anti-transient receptor potential cation channel, subfamily M, member 1 (TRPM1) autoantibodies showing concomitant Off-bipolar cell dysfunction.We evaluated
Autor:
Nancy Newman, Valerio Carelli, Patrick Yu-Wai-Man, Valerie Biousse, Mark Moster, Prem Subramanian, Catherine Vignal-Clermont, An-Guor Wang, Sean Donahue, Bart Leroy, Robert Sergott, Thomas Klopstock, Alfredo Sadun, Gema Rebolleda, Bart Chwalisz, Rudrani Banik, Magali Taiel, Jose-Alain Sahel
Publikováno v:
Monday, April 24.
Publikováno v:
Journal of Neuro-Ophthalmology.
Autor:
Yi-Ping Yang, Shania Foustine, Yu-Jer Hsiao, En-Tung Tsai, Fu-Ting Tsai, Chia-Lin Wang, Yu-Ling Ko, Hsiao-Yun Tai, Yi-Ching Tsai, Chang-Hao Yang, Yun-Ju Fu, An-Guor Wang, Yueh Chien
Publikováno v:
Journal of the Chinese Medical Association.