Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Chaw Liang Chang"'
Autor:
Yin-Hsiu Chien, Wen-Hui Tsai, Chaw-Liang Chang, Pao-Chin Chiu, Yen-Yin Chou, Fuu-Jen Tsai, Siew-Lee Wong, Ni-Chung Lee, Wuh-Liang Hwu
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 23, Iss , Pp - (2020)
Objective: Enzyme replacement therapy (ERT), the only approved therapy for infantile-onset Pompe disease (IOPD), had heterogeneous clinical effects due to factors such as severity, age at first treatment, dosage, and dosing regimens. We report the cl
Externí odkaz:
https://doaj.org/article/5372fb7ce94c44608bea42669b433dde
Publikováno v:
Circulation; 11/28/2023, Vol. 148 Issue 22, p1778-1796, 19p
Autor:
Yin-Hsiu Chien, Wuh-Liang Hwu, Ni-Chung Lee, Fuu-Jen Tsai, Dwight D. Koeberl, Wen-Hui Tsai, Pao-Chin Chiu, Chaw-Liang Chang
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 31-35 (2017)
Background: Early initiation of enzyme replacement therapy (ERT) with recombinant human acid alpha-glucosidase is an effective treatment for patients with infantile-onset Pompe disease (IOPD) but cannot prevent a slow progression of myopathy. Albuter
Externí odkaz:
https://doaj.org/article/1b01407f90ab444ba4fcb235b6b1f437
Publikováno v:
JAMA Network Open
This case-control study investigates the association of perinatal factors and maternal autoimmune diseases with the development of Kawasaki disease using the Taiwan Maternal and Child Health Database.
Publikováno v:
Environment International, Vol 118, Iss, Pp 97-105 (2018)
Background: Inorganic arsenic (iAs) exposure potentially causes diabetes and cardiovascular diseases in adults. However, its effect on glucose and lipid metabolism in early life remains unknown. Objective: We evaluated the associations between early-
Publikováno v:
Journal of Ultrasound in Medicine. 37:869-877
Objectives The aim of this study was to establish reference ranges for the corpus callosum in infancy and to clarify how sexual dimorphism evolves between the fetal stage and infancy. Methods Normal sonograms from cerebral ultrasonographic examinatio
Albuterol as an adjunctive treatment to enzyme replacement therapy in infantile-onset Pompe disease☆
Autor:
Ni-Chung Lee, Wen Hui Tsai, Yin-Hsiu Chien, Pao Chin Chiu, Dwight D. Koeberl, Chaw Liang Chang, Fuu Jen Tsai, Wuh-Liang Hwu
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 31-35 (2017)
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 31-35 (2017)
Background Early initiation of enzyme replacement therapy (ERT) with recombinant human acid alpha-glucosidase is an effective treatment for patients with infantile-onset Pompe disease (IOPD) but cannot prevent a slow progression of myopathy. Albutero
Publikováno v:
International Journal of Environmental Research and Public Health
International Journal of Environmental Research and Public Health, Vol 15, Iss 5, p 845 (2018)
International Journal of Environmental Research and Public Health; Volume 15; Issue 5; Pages: 845
International Journal of Environmental Research and Public Health, Vol 15, Iss 5, p 845 (2018)
International Journal of Environmental Research and Public Health; Volume 15; Issue 5; Pages: 845
Background: Countries at higher latitudes have higher incidence rates of Kawasaki disease (KD) than do countries at lower latitudes in the Asian and West Pacific area. However, the precise influence of latitude on KD incidence rates requires further
Publikováno v:
Pediatric Neurology. 52:192-197
Background Corpus callosum atrophy has been associated with cognitive and motor deficits in elderly people. However, the role of the corpus callosum in infant development is unclear. The aim of this study was to assess the impact of corpus callosum s
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine. 37(4)
The aim of this study was to establish reference ranges for the corpus callosum in infancy and to clarify how sexual dimorphism evolves between the fetal stage and infancy.Normal sonograms from cerebral ultrasonographic examinations of 1- to 6-month-