Research graph
References from A rare case of familial chylomicronemia in infancy due to homozygous <i>LMF1</i> variant. Local targets link to admitted publications; unresolved targets remain external evidence.
Primary hypertriglyceridemia in children and adolescents
10.1016/j.jacl.2015.04.004 · 2015 · External reference
Beyond the guidelines: perspectives on management of pediatric patients with hypertriglyceridemia
10.1007/s11883-024-01237-z · 2024 · External reference
Clinical and molecular spectrum of genetic hypertriglyceridaemia in North Indian children: a case series
10.5114/pedm.2025.148401 · 2025 · External reference
Comparison of patients with familial chylomicronemia syndrome and multifactorial chylomicronemia syndrome
10.1210/clinem/dgae613 · 2025 · External reference
Homozygous variant in LMF-1 identified in 3 Colombian families
10.1016/j.jacl.2026.01.005 · 2026 · External reference
Familial chylomicronemia syndrome: an expert clinical review from the National Lipid Association
10.1016/j.jacl.2025.03.013 · 2025 · External reference
Identification of compound heterozygous LMF1 variants in a patient with severe hypertriglyceridemia: case report and literature review
10.5551/jat.64697 · 2024 · External reference
A novel homozygous nonsense variant of LMF1 in pregnancy-induced hypertriglyceridemia with acute pancreatitis
10.1016/j.jacl.2023.03.005 · 2023 · External reference
Severe hypertriglyceridemia secondary to splice-site and missense variants in LMF1 in three patients from Ecuador
10.1016/j.jacl.2022.02.006 · 2022 · External reference
New rare genetic variants of LMF1 gene identified in severe hypertriglyceridemia
10.1016/j.jacl.2018.06.018 · 2018 · External reference
A compound heterozygous mutation of lipase maturation factor 1 is responsible for hypertriglyceridemia of a patient
10.5551/jat.44537 · 2019 · External reference
Characterization of two novel pathogenic variants at compound heterozygous status in lipase maturation factor 1 gene causing severe hypertriglyceridemia
10.1016/j.jacl.2018.07.008 · 2018 · External reference
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing
10.1016/j.jacl.2017.01.003 · 2017 · External reference
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia
10.1210/jc.2009-0594 · 2009 · External reference
Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia
10.1038/ng.2007.24 · 2007 · External reference
Fatty acids of human milk: a review
10.1024/0300-9831/a000651 · 2022 · External reference
Breast milk macronutrient components in prolonged lactation
10.3390/nu10121893 · 2018 · External reference
Components of human breast milk: from macronutrient to microbiome and microRNA
10.3345/cep.2020.00059 · 2020 · External reference
Unresolved reference
2025 · External reference
Dietary medium-chain triacylglycerols in metabolic regulation
10.1016/j.tem.2025.09.010 · 2026 · External reference
Apolipoprotein C-II: new findings related to genetics, biochemistry, and role in triglyceride metabolism
10.1016/j.atherosclerosis.2017.10.025 · 2017 · External reference
