Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jane H. Hsiao"'
Autor:
Ming-Shian Tsai, Meng-Larn Lee, Chun-Yun Chang, Hsiang-Hsuan Fan, I-Shing Yu, You-Tzung Chen, Jhih-Yi You, Chun-Yu Chen, Fang-Chia Chang, Jane H. Hsiao, Olga Khorkova, Horng-Huei Liou, Yuchio Yanagawa, Li-Jen Lee, Shu-Wha Lin
Publikováno v:
Neurobiology of Disease, Vol 77, Iss , Pp 35-48 (2015)
Dravet syndrome (DS) is characterized by severe infant-onset myoclonic epilepsy along with delayed psychomotor development and heightened premature mortality. A primary monogenic cause is mutation of the SCN1A gene, which encodes the voltage-gated so
Externí odkaz:
https://doaj.org/article/1c02147f797648a2b604654ad1313ea0
Autor:
Brian C Keller, Lourdes Bouzo-Lopez, Alejandro Gonzalez-De la Rosa, Juan C. Altamirano-Vallejo, Jose Navarro-Partida, Ana C Gonzalez-Villegas, Jose S Olguín-Gutierrez, Arturo Santos, Jane H. Hsiao
Publikováno v:
Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics. 34(5)
To achieve a safer alternative to intravitreal injection of corticosteroids, we developed and characterized triamcinolone acetonide-loaded liposomes formulations (TA-LFs) to be used topically for vitreoretinal drug delivery.Four different 0.2% TA-LFs
Autor:
Li-Jen Lee, Chun-Yu Chen, Fang-Chia Chang, Ming-Shian Tsai, Jane H. Hsiao, Shu-Wha Lin, Jhih-Yi You, You-Tzung Chen, Olga Khorkova, Horng-Huei Liou, I-Shing Yu, Chun-Yun Chang, Yuchio Yanagawa, Hsiang-Hsuan Fan, Meng-Larn Lee
Publikováno v:
Neurobiology of Disease, Vol 77, Iss, Pp 35-48 (2015)
Dravet syndrome (DS) is characterized by severe infant-onset myoclonic epilepsy along with delayed psychomotor development and heightened premature mortality. A primary monogenic cause is mutation of the SCN1A gene, which encodes the voltage-gated so