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- Six-year follow-up of a child with familial chylomicronemia syndrome: disease course and effectiveness of gemfibrozil treatment --case report and literature review
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Manal Mustafa
, Mira Almheiri - Ann Pediatr Endocrinol Metab. 2024;29(2):130-134. Published online January 15, 2024
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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
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