19 results on '"Niu, Dau-Ming"'
Search Results
2. Natural progression of cardiac features and long-term effects of enzyme replacement therapy in Taiwanese patients with mucopolysaccharidosis II
3. Hearing characteristics of infantile-onset Pompe disease after early enzyme-replacement therapy
4. Audiological and otologic manifestations of glutaric aciduria type I
5. Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985–2019)
6. Cardiac characteristics and natural progression in Taiwanese patients with mucopolysaccharidosis III
7. Methylmalonic acidemia/propionic acidemia – the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups
8. Cardiac features and effects of enzyme replacement therapy in Taiwanese patients with Mucopolysaccharidosis IVA
9. Clinical characteristics and surgical history of Taiwanese patients with mucopolysaccharidosis type II: data from the Hunter Outcome Survey (HOS)
10. A comparison of central nervous system involvement in patients with classical Fabry disease or the later-onset subtype with the IVS4+919G>A mutation.
11. Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta.
12. Methylmalonic acidemia/propionic acidemia - the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups.
13. Natural history and clinical assessment of Taiwanese patients with mucopolysaccharidosis IVA.
14. Globotriaosylsphingosine (lyso-Gb3) might not be a reliable marker for monitoring the long-term therapeutic outcomes of enzyme replacement therapy for late-onset Fabry patients with the Chinese hotspot mutation (IVS4+919G>A).
15. Endomyocardial biopsies in patients with left ventricular hypertrophy and a common Chinese later-onset Fabry mutation (IVS4 + 919G > A).
16. Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses.
17. A comparison of central nervous system involvement in patients with classical Fabry disease or the later-onset subtype with the IVS4+919G>A mutation.
18. Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995-2012.
19. Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.