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Cancer Genetics|January 2, 2022
Newly designed breakapart FISH probe helps to identify cases with true MECOM rearrangement in myeloid malignanciesMing Zhao, L Jeffrey Medeiros, Wei Wang, et al.
Journal of Inherited Metabolic Disease|October 7, 2010
Enzyme replacement therapy for mucopolysaccharidosis VI--experience in TaiwanHsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A|November 5, 2011
Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndromeDar-Shong Lin, Jui-Hsing Chang, Hsuan-Liang Liu, et al.
American Journal of Medical Genetics. Part A|August 3, 2018
Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21-year periodHsiang-Yu Lin, Chih-Kuang Chuang, Chung-Lin Lee, et al.
Palliative & Supportive Care|May 21, 2026
Frailty and the confidence to plan ahead: Decision-making self-efficacy and advance care planning among older adults receiving home healthcareChi Hsien Huang, Cheng-Pei Lin, Kelly Yen-Chih Chen, et al.
Translational Neurodegeneration|February 9, 2024
Microstructural integrity of the locus coeruleus and its tracts reflect noradrenergic degeneration in Alzheimer's disease and Parkinson's diseaseChen-Pei Lin, Irene Frigerio, John G J M Bol, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Functional independence of Taiwanese children with Prader-Willi syndromeChung-Lin Lee, Hsiang-Yu Lin, Li-Ping Tsai, et al.
Orphanet Journal of Rare Diseases|May 27, 2018
Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in TaiwanChih-Kuang Chuang, Hsiang-Yu Lin, Tuan-Jen Wang, et al.
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