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A 1-month-old infant with chylomicronemia due to |
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Mo Kyung Jung, Juhyun Jin, Hyun Ok Kim, Ahreum Kwon, Hyun Wook Chae, Seok Jin Kang, Duk Hee Kim, Ho-Seong Kim | |
Ann Pediatr Endocrinol Metab. 2017;22(1):68-71. Published online March 31, 2017 DOI: https://doi.org/10.6065/apem.2017.22.1.68 |
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A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis Familial chylomicronemia syndrome and response to medium-chain triglyceride therapy in an infant with novel mutations in GPIHBP1 Regulation of Interferon-stimulated Gene (<italic>ISG</italic>)<italic>12</italic>, <italic>ISG15</italic>, and <italic>MX1</italic> and <italic>MX2</italic> by Conceptus Interferons (IFNTs) in Bovine Uterine Epithelial Cells A case of severe chylomicronaemia syndrome, in a patient with normal lipoprotein lipase activity, due to a previously unidentified mutation in the GPIHBP1 gene Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene Differential Expression of <italic>PPARγ</italic>, <italic>FASN</italic>, and <italic>ACADM</italic> Genes in Various Adipose Tissues and <italic>Longissimus dorsi</italic> Muscle from Yanbian Yellow Cattle and Yan Yellow Cattle Brown Heroin-Associated Case Report of Acute Bronchitis Treated with Sleep in a 20-Year-Old Man, a 2-Month-Old Infant, and a 6-Month-Old Child Cardiac <sup>123</sup>I-metaiodobenzylguanidine Scintigraphy in a Patient with Familial Parkinsonism with <italic>Parkin</italic> Gene Mutation |