Showing results 1 to 7 of 7
Title | Author(s) | Issue Date | Views | |
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Congenital Myopathies are a Group of Phenotypically and Genetically Heterogeneous Diseases Proceeding/Conference:Hong Kong Medical Journal | 2016 | 18 | ||
Congenital myopathies: characteristic and subtypes in Hong Kong Proceeding/Conference:Neuromuscular Disorders | 2015 | 58 | ||
Klein Levin syndrome is a steroid-responsive, non-N-methyl-D-aspartate receptor-mediated encephalitis Proceeding/Conference:Hong Kong Medical Journal | 2012 | 25 | ||
Klein Levin Syndrome is a steroid-responsive, non-N-methyl-D-aspartate receptor-mediated encephalitis Proceeding/Conference:Developmental Medicine and Child Neurology | 2012 | 206 | ||
Myofibrillar myopathies: a clinicopathological study of 13 cases Proceeding/Conference:Asian and Oceanian Myology Center Annual Scentific Meeting, AOMC 2016 | 2016 | 24 | ||
Territory wide study of patients with dystrophinopathy in Hong Kong Proceeding/Conference:Neuromuscular Disorders | 2013 | 45 | ||
The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8 Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, &
Hong Kong College of Paediatric Nursing | 2019 |