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A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis
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
Annals of Pediatric Endocrinology & Metabolism. 2017;22(1):68   Crossref logo
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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   Crossref logo
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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   Crossref logo
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Four-month-old male infant with generalized muscle weakness
Neuropathology. 2002;22(4):365-366   Crossref logo
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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
Asian-Australasian Journal of Animal Sciences. 2013;26(6):795-803   Crossref logo
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A novel mutation in GPIHBP1 causes familial chylomicronemia syndrome
Journal of Clinical Lipidology. 2018;12(2):506-510   Crossref logo
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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   Crossref logo
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Interferon-β-1a
Reactions Weekly. 2019;1744(1):163-163   Crossref logo
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622 CHILHOOD-ONSET CHYLOMICRONEMIA WITH REDUCED PLASMA LPL ACTIVITY AND MASS: IDENTIFICATION OF A NOVEL GPIHBP1 MUTATION
Atherosclerosis Supplements. 2011;12(1):131   Crossref logo
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Successful Management of a 29-Day-Old Infant with Severe Hyperlipidemia from a Novel Homozygous Variant of GPIHBP1 Gene
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