CrossRef Text and Data Mining
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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 toGPIHBP1gene mutation treated by plasmapheresis
Annals of Pediatric Endocrinology & Metabolism. 2017;22(1):68   Crossref logo
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Acquired Chylomicronemia Due to Autoantibodies Against GPIHBP1
Journal of Clinical Lipidology. 2022;16(3):e46-e47   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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A nonsense germline mutation in the LPL gene in a 1-month-old infant: case report with review of literature
Bulletin of the National Research Centre. 2023;47(1):   Crossref logo
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Correction: A nonsense germline mutation in the LPL gene in a 1-month-old infant: case report with review of literature
Bulletin of the National Research Centre. 2023;47(1):   Crossref logo
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A very rare case of chylomicronemia revealed by cerebral thrombophlebitis in a 4-month-old infant
Annals of Medicine & Surgery. 2022;75:   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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A novel mutation in GPIHBP1 causes familial chylomicronemia syndrome
Journal of Clinical Lipidology. 2018;12(2):506-510   Crossref logo
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