Zobrazeno 1 - 10
of 158
pro vyhledávání: '"Tze-Wah Kao"'
Autor:
Jia-Lien Hsu, Anandakumar Singaravelan, Chih-Yun Lai, Zhi-Lin Li, Chia-Nan Lin, Wen-Shuo Wu, Tze-Wah Kao, Pei-Lun Chu
Publikováno v:
Bioengineering, Vol 11, Iss 10, p 963 (2024)
Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease leading to end-stage renal disease. Total kidney volume (TKV) measurement has been considered as a surrogate in the evaluation of disease sev
Externí odkaz:
https://doaj.org/article/06012075cf6c491ebab6ab32147deed3
Publikováno v:
Biomedical Journal, Vol 45, Iss 5, Pp 806-813 (2022)
Background: Few studies documented incidence rates of different types of stroke among patients with polycystic kidney disease (PKD). Methods: We conducted a retrospective cohort study based on the National Health Insurance (NHI) Database of Taiwan. T
Externí odkaz:
https://doaj.org/article/bf7d93ad1f3b4ae4a10ae1db7ee3ad1a
Autor:
Li-Kai Tsai, Pei-Lung Chen, Hsin-Hsi Tsai, Ya-Fang Chen, Ping-Chun Wu, Jiann-Shing Jeng, Jenq-Wen Huang, Tzong-Shinn Chu, Juliana Tze-Wah Kao
Publikováno v:
Journal of Stroke, Vol 22, Iss 1, Pp 153-156 (2020)
Externí odkaz:
https://doaj.org/article/bf3978d46b5a48059673fb1951cff9c3
Autor:
Angela Ju, Allison Tong, Armando Teixeira-Pinto, David Johnson, Jonathan Craig, Martin Howell, Ron T Gansevoort, Talia Gutman, Karine E Manera, Peter Kerr, Gopala K Rangan, Curie Ahn, Tess Harris, Charlotte Logeman, Yeoungjee Cho, Benedicte Sautenet, Albert Ong, Arlene Chapman, Helen Coolican, Juliana Tze-Wah Kao, Ronald Perrone, Vincent Torres, Kevin Fowler, York Pei, Jessica Ryan, Andrea Viecelli, Clair Geneste, Hyunsuk Kim, Yaerim Kim, Gayathri Parasivam
Publikováno v:
BMJ Open, Vol 10, Iss 10 (2020)
Background and objectives Presymptomatic testing is available for early diagnosis of hereditary autosomal dominant polycystic kidney disease (ADPKD). However, the complex ethical and psychosocial implications can make decision-making challenging and
Externí odkaz:
https://doaj.org/article/e8d547dcad65403eb9a4e532022791fc
Autor:
Jenq-Wen Huang, Hyunjin Ryu, Hayne C Park, Yun Kyu Oh, Irene Sangadi, Annette Wong, Changlin Mei, Tevfik Ecder, Tze-Wah Kao, Gopala K Rangan, Curie Ahn
Publikováno v:
BMJ Open, Vol 10, Iss 2 (2020)
IntroductionPatients with autosomal dominant polycystic kidney disease (ADPKD) reach end-stage renal disease in their fifth decade on average. For effective treatment and early intervention, identifying subgroups with rapid disease progression is imp
Externí odkaz:
https://doaj.org/article/c6f3edef768f47d895ab8b7e872a24a8
Publikováno v:
Biomedical Journal. 45:806-813
Background Few studies documented incidence rates of different types of stroke among patients with polycystic kidney disease (PKD). Materials and methods We conducted a retrospective cohort study based on the National Health Insurance (NHI) Database
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26d1059a7fea17230e2eb68b74130ef3
https://doi.org/10.1016/j.bj.2021.10.005
https://doi.org/10.1016/j.bj.2021.10.005
Autor:
Yeoungjee Cho, Benedicte Sautenet, Gopala Rangan, Jonathan C. Craig, Albert C. M. Ong, Arlene Chapman, Curie Ahn, Dongping Chen, Helen Coolican, Juliana Tze-Wah Kao, Ron Gansevoort, Ronald Perrone, Tess Harris, Vicente Torres, York Pei, Peter G. Kerr, Jessica Ryan, Talia Gutman, Martin Howell, Angela Ju, Karine E. Manera, Armando Teixeira-Pinto, Lorraine A. Hamiwka, Allison Tong
Publikováno v:
Trials, Vol 18, Iss 1, Pp 1-11 (2017)
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is the most common potentially life threatening inherited kidney disease and is responsible for 5–10% of cases of end-stage kidney disease (ESKD). Cystic kidneys may enlarge u
Externí odkaz:
https://doaj.org/article/d0852e92b5124aa291128181a39abb13
Autor:
Ching-Fang Wu, Yee-Fan Lee, Wen-Jeng Lee, Chi-Ting Su, Lukas Jyuhn-Hsiarn Lee, Kwan-Dun Wu, Pau-Chung Chen, Tze-Wah Kao
Publikováno v:
Journal of the Formosan Medical Association, Vol 116, Iss 5, Pp 366-372 (2017)
Vascular calcification can predict cardiovascular (CV) morbidity and mortality in patients with end-stage renal disease. We evaluated the prevalence, association factors, and outcomes of chest X-ray-detected aortic arch calcification (AoAC) in patien
Externí odkaz:
https://doaj.org/article/01366ed604ac4e3b8823eba9b4d2bded
Publikováno v:
Journal of the Formosan Medical Association, Vol 114, Iss 10, Pp 1008-1010 (2015)
A rare but severe complication, intestinal necrosis, has been reported after sodium polystyrene sulfonate (SPS; Kayexalate) and sorbitol intake. Some case reports described bowel perforation following calcium polystyrene sulfonate (CPS; Kalimate) adm
Externí odkaz:
https://doaj.org/article/8629831f77a94284ac27eea8804694a7
Autor:
Bénédicte Sautenet, Yeoungjee Cho, Talia Gutman, Gopala Rangan, Albert Ong, Arlene B. Chapman, Curie Ahn, Helen Coolican, Juliana Tze-Wah Kao, Kevin Fowler, Ron T. Gansevoort, Claire Geneste, Ronald D. Perrone, Tess Harris, Vicente E. Torres, York Pei, Jonathan C. Craig, Allison Tong, Arlene Chapman, Ron Gansevoort, Ronald Perrone, Vicente Torres, Benedicte Sautenet
Publikováno v:
American Journal of Kidney Diseases
American Journal of Kidney Diseases, Elsevier, 2020, ⟨10.1053/j.ajkd.2019.12.003⟩
American Journal of Kidney Diseases, Elsevier, 2020, ⟨10.1053/j.ajkd.2019.12.003⟩
Rationale & Objective:\ud Trials in autosomal dominant polycystic kidney disease (ADPKD) have increased, but their impact on decision making has been limited. Because heterogeneity in reported outcomes may be responsible, we assessed their range and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c58dca53f3bd9636a55398e9b6a3371
https://hdl.handle.net/11370/a6dcc131-c9f1-40a8-ae4f-1dde4830c96c
https://hdl.handle.net/11370/a6dcc131-c9f1-40a8-ae4f-1dde4830c96c