Browsing by Author "Lin, Ching-Chih"
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Item type:Item, Feasibility Study of Integrating Source Driver on Array Using Low-Temperature Polycrystalline Silicon Thin-Film Transistors(2016-12) ;Tai, Ya-Hsiang ;Lin, Ching-Chih ;Lin, Chi-Hao ;Chang, Chun-Yi光電工程學系In this paper, we proposed a new kind of source driver with fully digital driving and a new approach to implement source driver on array (SoA). For the SoA circuit, the digital/analogue converters and buffers are replaced with pulse width modulation circuit and data voltage setting circuit to simplify the source driver. Thus, the signal converting part in the conventional source driver can be omitted and is much more easy to be built with thin-film transistors on the glass. Further, the feasibility of integrating SoA will be studied in the practical way. The layout area and power consumption are found to be the obstacles if we want to use the current thin-film transistor technology to implement SoA. However, the fully digital driving concept can be still applied to develop the configuration of digital interface. We can use the external source driver to produce the digital pulse width signal to set the pixel voltage. This method avoids issue of layout area and power consumption. Hence, the concept of digital interface is much more practical and feasible to reduce the cost and power of data driving instead of SoA.Item type:Item, Feasibility Study of Integrating Source Driver on Array Using Low-Temperature Polycrystalline Silicon Thin-Film Transistors(2016-12) ;Tai, Ya-Hsiang ;Lin, Ching-Chih ;Lin, Chi-Hao ;Chang, Chun-Yi光電工程學系In this paper, we proposed a new kind of source driver with fully digital driving and a new approach to implement source driver on array (SoA). For the SoA circuit, the digital/analogue converters and buffers are replaced with pulse width modulation circuit and data voltage setting circuit to simplify the source driver. Thus, the signal converting part in the conventional source driver can be omitted and is much more easy to be built with thin-film transistors on the glass. Further, the feasibility of integrating SoA will be studied in the practical way. The layout area and power consumption are found to be the obstacles if we want to use the current thin-film transistor technology to implement SoA. However, the fully digital driving concept can be still applied to develop the configuration of digital interface. We can use the external source driver to produce the digital pulse width signal to set the pixel voltage. This method avoids issue of layout area and power consumption. Hence, the concept of digital interface is much more practical and feasible to reduce the cost and power of data driving instead of SoA.Item type:Item, Serial serologic changes of hepatitis D virus in chronic hepatitis B patients receiving nucleos(t)ides analogues therapy(1970-01-01) ;Jang, Tyng-Yuan ;Wei, Yu-Ju ;Hsu, Cheng-Ting ;Hsu, Po-YaoLiu, Ta-WeiBackground and Aim The serial serologic changes of hepatitis D virus (HDV) infection among chronic hepatitis B virus (HBV) infected patients who received oral nucleotide/nucleoside analogues are elusive. Methods Serum anti-HDV and HDV RNA among chronic hepatitis B (CHB) patients were tested at the time of initiating anti-HBV therapy and subsequently during the follow-up period. Results The seropositive rate of anti-HDV and HDV RNA among 2850 CHB patients, was 2.7% and 0.9%, respectively. Factors associated with anti-HDV seropositivity were platelet counts (odds ratio [OR]/95% confidence intervals [CI]: 0.995/0.992-0.999; P = 0.006), HBV DNA levels (OR/CI: 0.81/0.70-0.94; P = 0.005), and hepatitis B e-antigen (HBeAg) seropositivity (OR/CI: 0.22/0.05-0.95; P = 0.04). The only factor associated with HDV RNA positivity among anti-HDV seropositive patients was age (OR/CI: 0.95/0.90-1.00; P = 0.03). The spontaneous clearance rate of serum anti-HDV antibody was 3.0 per 100 person-years with a median follow-up period of 3.5 years (range 2-12 years), whereas the seroclearance rate of HDV RNA was 4.3 per 100 person-years among anti-HDV seropositive patients after a median follow-up period of 6.0 years (range 2-11 years). A baseline anti-HDV titer < 0.5 cut-off index was the only factor predictive of anti-HDV seroclearance (hazard ratio [HR]/CI: 30.11/3.73-242.85; P = 0.001). Conclusions HDV infection was not common among patients treated for HBV in Taiwan. Seroclearance of anti-HDV and HDV RNA did occur over time, albeit the chance is rare.