A 1-month-old infant with chylomicronemia due to
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 2017 Mar 31 DOI: https://doi.org/10.6065/apem.2017.22.1.68
|
Citations to this article as recorded by
Olezarsen, Acute Pancreatitis, and Familial Chylomicronemia Syndrome
Erik S.G. Stroes, Veronica J. Alexander, Ewa Karwatowska-Prokopczuk, Robert A. Hegele, Marcello Arca, Christie M. Ballantyne, Handrean Soran, Thomas A. Prohaska, Shuting Xia, Henry N. Ginsberg, Joseph L. Witztum, Sotirios Tsimikas
New England Journal of Medicine.2024; 390(19): 1781. CrossRef Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene
Ka Young Kim, You Joung Heo, Jung Min Ko, Young Ah Lee, Choong Ho Shin, Chang Seok Ki, Yun Jeong Lee
BMC Endocrine Disorders.2024;[Epub] CrossRef Clinical and molecular characterization of familial chylomicronemia in Saudi patients: a retrospective study
Abdullah Al-Ashwal, Manal AlHelal, Afaf AlSagheir, Areej Alfattani, Khushnooda Ramzan, Faiqa Imtiaz, Raghad Alhuthil
Frontiers in Endocrinology.2024;[Epub] CrossRef Inherited Lipid Disorders in Children: Experience from a Tertiary Care Centre
Simran Syal, Sudha Rao, Rajesh Joshi, Rachna Keshwani, Minnie Bodhanwala
Indian Journal of Endocrinology and Metabolism.2023; 27(3): 230. CrossRef Therapeutic plasma exchange for neonatal hepatic failure
Aviv Sever, Jerry Stein, Alon Kalo, Michal Pearl-Yafe, Gili Kadmon, Avichai Weissbach, Elhanan Nahum, Eytan Kaplan
Transfusion and Apheresis Science.2023; 62(6): 103810. CrossRef Case Report: Successful Management of a 29-Day-Old Infant With Severe Hyperlipidemia From a Novel Homozygous Variant of GPIHBP1 Gene
Shu Liu, Zhiqing Wang, Xianhua Zheng, Ye Zhang, Sisi Wei, Haimei OuYang, Jinqun Liang, Nuan Chen, Weihong Zeng, Jianhui Jiang
Frontiers in Pediatrics.2022;[Epub] CrossRef A homozygous variant in the GPIHBP1 gene in a child with severe hypertriglyceridemia and a systematic literature review
Ursa Sustar, Urh Groselj, Sabeen Abid Khan, Saeed Shafi, Iqbal Khan, Jernej Kovac, Barbara Jenko Bizjan, Tadej Battelino, Fouzia Sadiq
Frontiers in Genetics.2022;[Epub] CrossRef Volanesorsen in the Treatment of Familial Chylomicronemia Syndrome or Hypertriglyceridaemia: Design, Development and Place in Therapy Oluwayemisi Esan, Anthony S Wierzbicki
Drug Design, Development and Therapy.2020; Volume 14: 2623. CrossRef Gpihbp1 deficiency accelerates atherosclerosis and plaque instability in diabetic Ldlr-/- mice
Xuejing Liu, Jingyi Li, Jiawei Liao, Huan Wang, Xiaomin Huang, Zhao Dong, Qiang Shen, Ling Zhang, Yuhui Wang, Wei Kong, George Liu, Wei Huang
Atherosclerosis.2019; 282: 100. CrossRef Therapeutic Plasma‐albumin Exchange for Hyperlipidemia Induced Acute Pancreatitis
Stavroula Ilia, Elisavet Geromarkaki, Marianna Miliaraki, George Briassoulis
Journal of Pediatric Gastroenterology and Nutrition.2018;[Epub] CrossRef Familial chylomicronemia – a rare cause of dyslipidemia in newborn
Ioana Țieranu, Maria Gica, Adrian Stanciu, Mihaela Bălgrădean
Pediatru.ro.2018; 4(52): 44. CrossRef
|