Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: Pancreatitis and LPL[original query] |
---|
Association analysis among polymorphisms of the various genes and chronic alcoholic pancreatitis. Journal of gastroenterology and hepatology 2008 Mar 23 Suppl 1 S69-72. Maruyama Katsuya, Harada Shoji, Yokoyama Akira, Naruse Satoru, Hirota Masahiko, Nishimori Isao, Otsuki Mako |
Association analyses of genetic polymorphisms of GSTM1, GSTT1, NQO1, NAT2, LPL, PRSS1, PSTI, and CFTR with chronic alcoholic pancreatitis in Japan. Alcoholism, clinical and experimental research 2010 Feb 34 Suppl 1 S34-8. Maruyama Katsuya, Harada Shoji, Yokoyama Akira, Mizukami Satoshi, Naruse Satoru, Hirota Masahiko, Nishimori Isao, Otsuki Mako |
Lipoprotein lipase mutation S447X associated with pancreatic calcification and steatorrhea in hyperlipidemic pancreatitis. Journal of clinical gastroenterology 2009 Jul 43 (6): 591-6. Chang Yu-Ting, Chang Ming-Chu, Su Ta-Chen, Liang Po-Chin, Su Yi-Ning, Kuo Chun-Hung, Wei Shu-Chen, Wong Jau-M |
Lipoprotein lipase activity and mass, apolipoprotein C-II mass and polymorphisms of apolipoproteins E and A5 in subjects with prior acute hypertriglyceridaemic pancreatitis. BMC gastroenterology 2009 9 . Coca-Prieto I, Valdivielso P, Olivecrona G, Ariza MJ, Rioja J, Font-Ugalde P, García-Arias C, González-Santos P |
The g.-469G>A polymorphism in the GPIHBP1 gene promoter is associated with hypertriglyceridemia and has an additive effect on the risk conferred by LPL defective alleles. Nutrition, metabolism, and cardiovascular diseases : NMCD 2013 Apr 23 (4): 358-65. Guay S P, Gaudet D, Brisson |
Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia. Journal of internal medicine 2012 Aug 272 (2): 185-96. Surendran R P, Visser M E, Heemelaar S, Wang J, Peter J, Defesche J C, Kuivenhoven J A, Hosseini M, Péterfy M, Kastelein J J P, Johansen C T, Hegele R A, Stroes E S G, Dallinga-Thie G |
[Hypertriglyceridemia-induced pancreatitis]. Nihon rinsho. Japanese journal of clinical medicine 2013 Sep 71 (9): 1602-5. Nagayama Daiji, Shirai Koh |
Genetic Variants Associated with Gestational Hypertriglyceridemia and Pancreatitis. PloS one 2015 10 (6): e0129488. Xie Sai-Li, Chen Tan-Zhou, Huang Xie-Lin, Chen Chao, Jin Rong, Huang Zhi-Ming, Zhou Meng-T |
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia. Atherosclerosis 2015 Jul 241 (1): 79-86. Rabacchi Claudio, Pisciotta Livia, Cefalù Angelo B, Noto Davide, Fresa Raffaele, Tarugi Patrizia, Averna Maurizio, Bertolini Stefano, Calandra Sebastia |
Rare genetic variants with large effect on triglycerides in subjects with a clinical diagnosis of familial vs nonfamilial hypertriglyceridemia. Journal of clinical lipidology 0 10 (4): 790-7. De Castro-Orós Isabel, Civeira Fernando, Pueyo María Jesús, Mateo-Gallego Rocío, Bolado-Carrancio Alfonso, Lamíquiz-Moneo Itziar, Álvarez-Sala Luis, Fabiani Fernando, Cofán Montserrat, Cenarro Ana, Rodríguez-Rey José Carlos, Ros Emilio, Pocoví Migu |
Association of the HindIII Lipoprotein Lipase Gene Polymorphism with the Development of the Non-Biliary Acute Pancreatitis: a Pilot Study. Bulletin of experimental biology and medicine 2016 Jun . Samgina T A, Bushueva O Yu, Nazarenko P M, Polonikov A |
Hypertriglyceridemic acute pancreatitis in emergency department: Typical clinical features and genetic variants. Journal of digestive diseases 2017 Jun 18 (6): 359-368. Chen Wan Jun, Sun Xiao Fan, Zhang Rui Xue, Xu Min Jie, Dou Tong Hai, Zhang Xiao Bin, Zhong Min, Yang Wei Qiang, Liu Li, Lu Xiao Ye, Zhu Chang Qi |
Molecular and functional characterization of familial chylomicronemia syndrome. Atherosclerosis 2017 11 269 272-278. Teramoto Ryota, Tada Hayato, Kawashiri Masa-Aki, Nohara Atsushi, Nakahashi Takuya, Konno Tetsuo, Inazu Akihiro, Mabuchi Hiroshi, Yamagishi Masakazu, Hayashi Kens |
Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an "FCS score". Atherosclerosis 2018 7 275 265-272. Moulin Philippe, Dufour Robert, Averna Maurizio, Arca Marcello, Cefalù Angelo B, Noto Davide, D'Erasmo Laura, Di Costanzo Alessia, Marçais Christophe, Alvarez-Sala Walther Luis Antonio, Banach Maciej, Borén Jan, Cramb Robert, Gouni-Berthold Ioanna, Hughes Elizabeth, Johnson Colin, Pintó Xavier, Reiner Ċ½eljko, van Lennep Jeanine Roeters, Soran Handrean, Stefanutti Claudia, Stroes Erik, Bruckert Er |
Compound but non-linked heterozygous p.W14X and p.L279 V LPL gene mutations in a Chinese patient with long-term severe hypertriglyceridemia and recurrent acute pancreatitis. Lipids in health and disease 2018 6 17 (1): 144. Li Xiaoyao, Yang Qi, Shi Xiaolei, Chen Weiwei, Pu Na, Li Weiqin, Li Jiesh |
Acute pancreatitis secondary to oral contraceptive-induced hypertriglyceridemia: a case report. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2018 5 34 (11): 930-932. Stumpf Matheo Augusto Morandi, Kluthcovsky Ana Claudia Garabeli Cavalli, Okamoto Jefferson Matsuiti, Schrut Gianna Carla Alberti, Cajoeiro Patricia de Oliveira, Chacra Ana Paula Marte, Bizeli Ricar |
Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitis. EBioMedicine 2018 Dec 38 171-177. Jin Jing-Lu, Sun Di, Cao Ye-Xuan, Zhang Hui-Wen, Guo Yuan-Lin, Wu Na-Qiong, Zhu Cheng-Gang, Gao Ying, Dong Qiu-Ting, Liu Geng, Dong Qian, Li Jian-J |
Characterizing familial chylomicronemia syndrome: Baseline data of the APPROACH study. Journal of clinical lipidology 2018 10 12 (5): 1234-1243.e5. Blom Dirk J, O'Dea Louis, Digenio Andres, Alexander Veronica J, Karwatowska-Prokopczuk Ewa, Williams Karren R, Hemphill Linda, Muñiz-Grijalvo Ovidio, Santos Raul D, Baum Seth, Witztum Joseph |
Identification of a novel and heterozygous LMF1 nonsense mutation in an acute pancreatitis patient with severe hypertriglyceridemia, severe obesity and heavy smoking. Lipids in health and disease 2019 3 18 (1): 68. Chen Wei-Wei, Yang Qi, Li Xiao-Yao, Shi Xiao-Lei, Pu Na, Lu Guo-Tao, Tong Zhi-Hui, Chen Jian-Min, Li Wei-Q |
Spectrum of Mutations and Long-Term Clinical Outcomes in Genetic Chylomicronemia Syndromes. Arteriosclerosis, thrombosis, and vascular biology 2019 10 39 (12): 2531-2541. D'Erasmo Laura, Di Costanzo Alessia, Cassandra Francesca, Minicocci Ilenia, Polito Luca, Montali Anna, Ceci Fabrizio, Arca Marcel |
Genetic Variants Associated With Increased Plasma Levels of Triglycerides, via Effects on the Lipoprotein Lipase Pathway, Increase Risk of Acute Pancreatitis. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2020 Aug . Hansen Signe E J, Madsen Christian M, Varbo Anette, Tybjærg-Hansen Anne, Nordestgaard Børge |
Genetic and functional studies of the LMF1 gene in Thai patients with severe hypertriglyceridemia. Molecular genetics and metabolism reports 2020 3 23 100576. Plengpanich Wanee, Muanpetch Suwanna, Charoen Supannika, Kiateprungvej Arunrat, Khovidhunkit Weerap |
Rare Variants in Triglycerides-Related Genes Increase Pancreatitis Risk in Multifactorial Chylomicronemia Syndrome. The Journal of clinical endocrinology and metabolism 2021 5 106 (9): e3473-e3482. Paquette Martine, Amyot Julie, Fantino Manon, Baass Alexis, Bernard Soph |
Clinical heterogeneity in monogenic chylomicronaemia. BMJ case reports 2022 11 15 (11): . Heidemann Britt E, Bemelmans Remy H H, Marais A David, Visseren Frank L J, Koopal Charlot |
Clinical and Genetic Description of Hereditary Chronic Pancreatitis in Pakistani Children. The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2023 8 . Huma Arshad Cheema, Zafar Fayyaz, Anjum Saeed, Muhammad Nadeem Anjum, Sadaqat Ijaz, Muhammad Arshad Alvi, Syeda Sara L Bat |
Frameshift coding sequence variants in the LPL gene: identification of two novel events and exploration of the genotype-phenotype relationship for variants reported to date. Lipids in health and disease 2023 8 22 (1): 128. Guofu Zhang, Yuepeng Hu, Qi Yang, Na Pu, Gang Li, Jingzhu Zhang, Zhihui Tong, Emmanuelle Masson, David N Cooper, Jian-Min Chen, Weiqin |
Post-prandial analysis of fluctuations in the platelet count and platelet function in patients with the familial chylomicronemia syndrome. Orphanet journal of rare diseases 2023 6 18 (1): 167. Miriam Larouche, Diane Brisson, Marie-Claude Morissette, Daniel Gaud |
Evinacumab in severe hypertriglyceridemia with or without lipoprotein lipase pathway mutations: a phase 2 randomized trial. Nature medicine 2023 3 . Rosenson Robert S, Gaudet Daniel, Ballantyne Christie M, Baum Seth J, Bergeron Jean, Kershaw Erin E, Moriarty Patrick M, Rubba Paolo, Whitcomb David C, Banerjee Poulabi, Gewitz Andrew, Gonzaga-Jauregui Claudia, McGinniss Jennifer, Ponda Manish P, Pordy Robert, Zhao Jian, Rader Daniel |
Loss-of-Function Homozygous Variant in LPL Causes Type I Hyperlipoproteinemia and Renal Lipidosis. Kidney international reports 2023 11 8 (11): 2428-2438. Hongyan Wu, Huan Xu, Song Lei, Zhi Yang, Shan Yang, Jingxue Du, Yi Zhou, Yunqiang Liu, Yuan Yang, Zhangxue |
Genetic Variants Associated with Severe Hypertriglyceridemia: LPL, APOC2, APOA5, GPIHBP1, LMF1, and APOE. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2023 1 51 (1): 10-21. Abedi Amir Hossein, Y?ld?r?m ?im?ir Ilg?n, Bayram Fahri, Onay Huseyin, Özgür Su, Mcintyre Adam, Toth Peter, Hegele Robe |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: