Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and LMF1[original query] |
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Clinical and biochemical features of different molecular etiologies of familial chylomicronemia. Journal of clinical lipidology 2018 Apr . Hegele Robert A, Berberich Amanda J, Ban Matthew R, Wang Jian, Digenio Andres, Alexander Veronica J, D'Erasmo Laura, Arca Marcello, Jones Alan, Bruckert Eric, Stroes Erik S, Bergeron Jean, Civeira Fernando, Witztum Joseph L, Gaudet Dani |
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 |
Genetics of Hypertriglyceridemia. Frontiers in endocrinology 2020 8 11 455. Dron Jacqueline S, Hegele Robert |
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 |
Identification of genetic variants related to metabolic syndrome by next-generation sequencing. Diabetology & metabolic syndrome 2022 Aug 14 (1): 119. Lee Sanghoo, Kim Seol-A, Hong Jeonghoon, Kim Yejin, Hong Gayeon, Baik SaeYun, Choi Kyeonghwan, Lee Mi-Kyeong, Lee Kyoung-Ry |
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