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Chou JY, Kim GY, Cho JH. Recent development and gene therapy for glycogen storage disease type Ia. Liver Res. 2017;1(3): 174-180.ChouJYKimGYChoJHRecent development and gene therapy for glycogen storage disease type IaLiver Res20171317418010.1016/j.livres.2017.12.001Search in Google Scholar
Shah MH, Roshan R, Desai R, Kadam SS. Neonatal hyperlipidemia with pancreatitis: novel gene mutation of lipoprotein lipase. J Postgrad Med. 2018; 64(4): 247-249.ShahMHRoshanRDesaiRKadamSSNeonatal hyperlipidemia with pancreatitis: novel gene mutation of lipoprotein lipaseJ Postgrad Med201864424724910.4103/jpgm.JPGM_731_17Search in Google Scholar
Gao M, Yang C, Wang X, et al. ApoC2 deficiency elicits severe hypertriglyceridemia and spontaneous atherosclerosis: A rodent model rescued from neonatal death. Metabolism. 2020; 109: 154296.GaoMYangCWangXet alApoC2 deficiency elicits severe hypertriglyceridemia and spontaneous atherosclerosis: A rodent model rescued from neonatal deathMetabolism202010915429610.1016/j.metabol.2020.154296Search in Google Scholar
Siafakas CG, Brown MR, Miller TL. Neonatal pancreatitis associated with familial lipoprotein lipase deficiency. J Pediatr Gastroenterol Nutr. 1999; 29(1): 95-98.SiafakasCGBrownMRMillerTLNeonatal pancreatitis associated with familial lipoprotein lipase deficiencyJ Pediatr Gastroenterol Nutr1999291959810.1097/00005176-199907000-00023Search in Google Scholar
Yıldız Y, Uysal Yazıcı M, Çınar HG, Özbay Hoşnut F, Kurt Çolak F, Kılıç M. Successful management of acute pancreatitis due to apolipoprotein C-II deficiency in a 37-day-old infant. Pancreatology. 2020; 20(4): 644-646.YıldızYUysalYazıcı MÇınarHGÖzbayHoşnut FKurtÇolak FKılıçMSuccessful management of acute pancreatitis due to apolipoprotein C-II deficiency in a 37-day-old infantPancreatology202020464464610.1016/j.pan.2020.03.008Search in Google Scholar
Chou JY, Mansfield BC. Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease. Hum Mutat. 2008; 29(7): 921-930.ChouJYMansfieldBCMutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage diseaseHum Mutat200829792193010.1002/humu.20772Search in Google Scholar
Talente GM, Coleman RA, Alter C, Baker L, Brown BI, Cannon RA, Chen YT, Crigler JF Jr, Ferreira P, Haworth JC, Herman GE, Issenman RM, Keating JP, Linde R, Roe TF, Senior B, Wolfsdorf JI: Glycogen storage disease in adults. Ann Intern Med. 1994; 120(4): 218-226.TalenteGMColemanRAAlterCBakerLBrownBICannonRAChenYTCriglerJF JrFerreiraPHaworthJCHermanGEIssenmanRMKeatingJPLindeRRoeTFSeniorBWolfsdorfJIGlycogen storage disease in adultsAnn Intern Med1994120421822610.7326/0003-4819-120-3-199402010-00008Search in Google Scholar
Bandsma RH, Prinsen BH, van Der Velden Mde S, Rake JP, Boer T, Smit GP, Reijngoud DJ, Kuipers F: Increased de novo lipogenesis and delayed conversion of large VLDL into intermediate density li-poprotein particles contribute to hyperlipidemia in glycogen storage disease type 1a. Pediatr Res. 2008; 63(6): 702-707.BandsmaRHPrinsenBHvanDer Velden Mde SRakeJPBoerTSmitGPReijngoudDJKuipersFIncreased de novo lipogenesis and delayed conversion of large VLDL into intermediate density li-poprotein particles contribute to hyperlipidemia in glycogen storage disease type 1aPediatr Res200863670270710.1203/PDR.0b013e31816c9013Search in Google Scholar
Carvalho PMS, Silva NJM, Dias PGD, Porto JFC, Santos LC, Costa JMN. Glycogen Storage Disease type 1a - a secondary cause for hyperlipidemia: report of five cases. J Diabetes Metab Disord. 2013; 12(1): 25.CarvalhoPMSSilvaNJMDiasPGDPortoJFCSantosLCCostaJMNGlycogen Storage Disease type 1a - a secondary cause for hyperlipidemia: report of five casesJ Diabetes Metab Disord20131212510.1186/2251-6581-12-25Search in Google Scholar
Koeberl DD, Kishnani PS, Bali D, Chen Y-T. Emerging therapies for glycogen storage disease type I. Trends Endocrinol Metab. 2009; 20(5): 252-258.KoeberlDDKishnaniPSBaliDChenY-TEmerging therapies for glycogen storage disease type ITrends Endocrinol Metab200920525225810.1016/j.tem.2009.02.003Search in Google Scholar