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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 | |
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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 Annals of Pediatric Endocrinology & Metabolism. 2017;22(1):68  Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene Journal of Clinical Lipidology. 2016;10(4):915-921.e4 Familial chylomicronemia syndrome and response to medium-chain triglyceride therapy in an infant with novel mutations in GPIHBP1 Journal of Clinical Lipidology. 2014;8(6):635-639 Four-month-old male infant with generalized muscle weakness Neuropathology. 2002;22(4):365-366 A novel mutation in GPIHBP1 causes familial chylomicronemia syndrome Journal of Clinical Lipidology. 2018;12(2):506-510 A case of severe chylomicronaemia syndrome, in a patient with normal lipoprotein lipase activity, due to a previously unidentified mutation in the GPIHBP1 gene Atherosclerosis. 2016;252:e72-e73 622 CHILHOOD-ONSET CHYLOMICRONEMIA WITH REDUCED PLASMA LPL ACTIVITY AND MASS: IDENTIFICATION OF A NOVEL GPIHBP1 MUTATION Atherosclerosis Supplements. 2011;12(1):131 Homozygous ARHGDIA Gene Mutation in an 11-Month-Old Infant with Steroid-Resistant Nephrotic Syndrome Indian Journal of Pediatrics. 2022;89(4):411-411 Interferon-β-1a Reactions Weekly. 2019;1744(1):163-163 Successful Management of a 29-Day-Old Infant with Severe Hyperlipidemia from a Novel Homozygous Variant of GPIHBP1 Gene . 2021; |
