Zobrazeno 1 - 10
of 257
pro vyhledávání: '"Chi Chao Chao"'
Diflunisal versus tafamidis on neuropathy and cardiomyopathy in hereditary transthyretin amyloidosis
Autor:
Chi‐Chao Chao, Shiou‐Ru Tzeng, Ming‐Chang Chiang, Hsueh‐Wen Hsueh, Wan‐Jen Hsieh, Yuan‐Chun Chao, Mei‐Fang Cheng, Yen‐Hung Lin, Mao‐Yuan Su, Chun‐Hsiang Huang, Yi‐Shiang Wang, Ming‐Fang Hsieh, Ping‐Huei Tseng, Sung‐Tsang Hsieh
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 9, Pp 2426-2438 (2024)
Abstract Objectives Hereditary transthyretin (TTR) amyloidosis (ATTRv) is frequently complicated by polyneuropathy (ATTRv‐PN) and cardiomyopathy (ATTRv‐CM). The long‐term efficacy of diflunisal on both polyneuropathy and cardiomyopathy in ATTRv
Externí odkaz:
https://doaj.org/article/e90951ed776746d3b147155bed8adf56
Autor:
Kon-Ping Lin, Chih-Chao Yang, Yi-Chung Lee, Ming-Jen Lee, John Vest, Marianne T. Sweetser, Matthew T. White, Prajakta Badri, Sung-Tsang Hsieh, Chi-Chao Chao
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 9, Pp 975-984 (2024)
Background: To examine the efficacy and safety of patisiran, an RNA interference therapeutic, in patients from Taiwan with hereditary transthyretin-mediated (hATTR) amyloidosis with polyneuropathy. Methods: The APOLLO phase 3 trial included patients
Externí odkaz:
https://doaj.org/article/dab5699cac1045209b1a2938728fe680
Autor:
Szu-Yu Pan, Thomas Tao-Min Huang, Yi-Chan Lin, Hui-Ting Liu, Sheng-Chieh Chou, Chih-Yuan Lee, Chien-Chia Chen, Chuan-Hsiu Fu, Chi-Chao Chao, Vin-Cent Wu
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 8, Pp 899-903 (2024)
Background/Purpose: Double-filtration plasmapheresis (DFPP) can be used to remove circulating pathogenic molecules. By reclaiming filtered albumin, DFPP reduces the need for albumin and plasma replacement. Large proteins, such as fibrinogen, are remo
Externí odkaz:
https://doaj.org/article/2d6b4d7df250458397fe7560e4b9fbc0
Autor:
Anke Ninija Karabanov, Rainer Paine, Chi Chao Chao, Katrin Schulze, Brian Scott, Mark Hallett, Mortimer Mishkin
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0119472 (2015)
Accumulating evidence suggests that storing speech sounds requires transposing rapidly fluctuating sound waves into more easily encoded oromotor sequences. If so, then the classical speech areas in the caudalmost portion of the temporal gyrus (pSTG)
Externí odkaz:
https://doaj.org/article/42c510a8554f411aa70d6867018c8218
Autor:
Marco Luigetti, Dianna Quan, John L. Berk, Isabel Conceição, Yohei Misumi, Chi-Chao Chao, Shaun Bender, Emre Aldinc, John Vest, David Adams
Publikováno v:
Neurology and Therapy, Vol 13, Iss 3, Pp 625-639 (2024)
Abstract Introduction Hereditary transthyretin (ATTRv, v for variant) amyloidosis is a rare, progressive, fatal disease with multisystem manifestations, caused by pathogenic variants in the transthyretin (TTR) gene. Vutrisiran, an RNA interference th
Externí odkaz:
https://doaj.org/article/60ae68c6fd63459e8e8e5e819c0f290b
Autor:
Chieh-Chang Chen, Ping-Huei Tseng, Hsueh-Wen Hsueh, Ming-Chang Chiang, Shiou-Ru Tzeng, Tsung Hsien Chiang, Ming-Shiang Wu, Sung-Tsang Hsieh, Chi-Chao Chao
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Increasing evidence suggests that gut microbiota alterations are related to development and phenotypes of many neuropsychiatric diseases. Here, we evaluated the fecal microbiota and its clinical correlates in patients with hereditary transth
Externí odkaz:
https://doaj.org/article/10793ad49d8c462cb55dd525060a85f4
Autor:
Shin‐Joe Yeh, Ti‐Yen Yeh, Yi‐Shiang Wang, Chi‐Chao Chao, Shiou‐Ru Tzeng, Tsz‐Yi Tang, Jung‐Hsien Hsieh, Yu‐Yu Kan, Wei‐Kang Yang, Sung‐Tsang Hsieh
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 1, Pp 30-44 (2024)
Abstract Objective Despite amyloid deposition as a hallmark of hereditary transthyretin amyloidosis (ATTRv) with polyneuropathy, this pathology could not completely account for nerve degeneration. ATTRv patients frequently have vasomotor symptoms, bu
Externí odkaz:
https://doaj.org/article/b7bb943dad7c4f60a68924fac1a7ae26
Autor:
Cheng-Hsuan Tsai, Chi-Chao Chao, Sung-Tsang Hsieh, An-Li Yu, Yuan-Kun (Aden) Wu, Mei-Fang Cheng, Ming-Jen Lee, Chia-Hung Chou, Chia-Tung Shun, Hsueh-Wen Hsueh, Jimmy Jyh-Ming Juang, Ping-Huei Tseng, Mao-Yuan Su, Yen-Hung Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-9 (2023)
Abstract Background Transthyretin cardiac cardiomyopathy (ATTR-CM) is a rare but life-threatening disease. Tafamidis is an effective treatment for patients with ATTR-CM, however its long-term effects on cardiac remodeling and cardiac amyloid depositi
Externí odkaz:
https://doaj.org/article/7b717f17a27e4e59a7dce2d5867ada04
Autor:
Sung‐Ju Hsueh, Chi‐Chao Chao, Ta‐Fu Chen, Ya‐Fang Chen, Hsueh‐Wen Hsueh, Li‐Kai Tsai, Wen‐Chau Wu, Sung‐Tsang Hsieh
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 8, Pp 1456-1466 (2023)
Abstract Objective This study aimed to explore the clinical significance of brain imaging signatures in the context of clinical neurological deficits in association with upper and lower motor neuron degeneration in amyotrophic lateral sclerosis (ALS)
Externí odkaz:
https://doaj.org/article/c854fa4275a240a78814a6fda65c39d3
Autor:
An‐Li Yu, Yi‐Chieh Chen, Cheng‐Hsuan Tsai, Yuan‐Kun Aden Wu, Mao‐Yuan Su, Chia‐Hung Chou, Chia‐Tung Shun, Hsueh‐Wen Hsueh, Jimmy Jyh‐Ming Juang, Ming‐Jen Lee, Ping‐Huei Tseng, Chia‐Hua Hsu, Sung‐Tsang Hsieh, Chi‐Lun Ko, Mei‐Fang Cheng, Chi‐Chao Chao, Yen‐Hung Lin
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 2 (2024)
Background Hereditary transthyretin amyloid cardiomyopathy (hATTR‐CM) is a progressive and fatal disease. Recent evidence indicates that bone scintigraphy may serve as a tool to monitor the effectiveness of hATTR‐CM treatment. The objective of th
Externí odkaz:
https://doaj.org/article/d46e9b051b124a0385d92f5c1905068b