183 related articles for article (PubMed ID: 28391895)
1. Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.
Cefalù AB; Spina R; Noto D; Ingrassia V; Valenti V; Giammanco A; Fayer F; Misiano G; Cocorullo G; Scrimali C; Palesano O; Altieri GI; Ganci A; Barbagallo CM; Averna MR
J Clin Lipidol; 2017; 11(1):272-281.e8. PubMed ID: 28391895
[TBL] [Abstract][Full Text] [Related]
2. Frequency of rare mutations and common genetic variations in severe hypertriglyceridemia in the general population of Spain.
Lamiquiz-Moneo I; Blanco-Torrecilla C; Bea AM; Mateo-Gallego R; Pérez-Calahorra S; Baila-Rueda L; Cenarro A; Civeira F; de Castro-Orós I
Lipids Health Dis; 2016 Apr; 15():82. PubMed ID: 27108409
[TBL] [Abstract][Full Text] [Related]
3. A Compound Heterozygous Mutation of Lipase Maturation Factor 1 is Responsible for Hypertriglyceridemia of a Patient.
Liu Y; Xu J; Tao W; Yu R; Zhang X
J Atheroscler Thromb; 2019 Feb; 26(2):136-144. PubMed ID: 29910226
[TBL] [Abstract][Full Text] [Related]
4. Identification of a novel and heterozygous LMF1 nonsense mutation in an acute pancreatitis patient with severe hypertriglyceridemia, severe obesity and heavy smoking.
Chen WW; Yang Q; Li XY; Shi XL; Pu N; Lu GT; Tong ZH; Chen JM; Li WQ
Lipids Health Dis; 2019 Mar; 18(1):68. PubMed ID: 30885219
[TBL] [Abstract][Full Text] [Related]
5. Involvement of a homozygous exon 6 deletion of LMF1 gene in intermittent severe hypertriglyceridemia.
Serveaux Dancer M; Marmontel O; Wozny AS; Marcais C; Mahl M; Dumont S; Simonet T; Moulin P; Di Filippo M; Charrière S
J Clin Lipidol; 2020; 14(6):756-761. PubMed ID: 33039347
[TBL] [Abstract][Full Text] [Related]
6. [Identification of variants in LMF1 gene associated with primary hypertriglyceridemia].
Lamiquiz-Moneo I; Bea AM; Mateo-Gallego R; Baila-Rueda L; Cenarro A; Pocoví M; Civeira F; de Castro-Orós I
Clin Investig Arterioscler; 2015; 27(5):246-52. PubMed ID: 25817768
[TBL] [Abstract][Full Text] [Related]
7. Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia.
Rabacchi C; Pisciotta L; Cefalù AB; Noto D; Fresa R; Tarugi P; Averna M; Bertolini S; Calandra S
Atherosclerosis; 2015 Jul; 241(1):79-86. PubMed ID: 25966443
[TBL] [Abstract][Full Text] [Related]
8. Severe hypertriglyceridemia is primarily polygenic.
Dron JS; Wang J; Cao H; McIntyre AD; Iacocca MA; Menard JR; Movsesyan I; Malloy MJ; Pullinger CR; Kane JP; Hegele RA
J Clin Lipidol; 2019; 13(1):80-88. PubMed ID: 30466821
[TBL] [Abstract][Full Text] [Related]
9. Incidental finding of severe hypertriglyceridemia in children. Role of multiple rare variants in genes affecting plasma triglyceride.
Buonuomo PS; Rabacchi C; Macchiaiolo M; Trenti C; Fasano T; Tarugi P; Bartuli A; Bertolini S; Calandra S
J Clin Lipidol; 2017; 11(6):1329-1337.e3. PubMed ID: 28951076
[TBL] [Abstract][Full Text] [Related]
10. Molecular and functional characterization of familial chylomicronemia syndrome.
Teramoto R; Tada H; Kawashiri MA; Nohara A; Nakahashi T; Konno T; Inazu A; Mabuchi H; Yamagishi M; Hayashi K
Atherosclerosis; 2018 Feb; 269():272-278. PubMed ID: 29153744
[TBL] [Abstract][Full Text] [Related]
11. Partial
Dron JS; Wang J; McIntyre AD; Cao H; Robinson JF; Duell PB; Manjoo P; Feng J; Movsesyan I; Malloy MJ; Pullinger CR; Kane JP; Hegele RA
J Lipid Res; 2019 Nov; 60(11):1953-1958. PubMed ID: 31519763
[TBL] [Abstract][Full Text] [Related]
12. Genetic Variants Associated with Severe Hypertriglyceridemia: LPL, APOC2, APOA5, GPIHBP1, LMF1, and APOE.
Abedi AH; Yıldırım Şimşir I; Bayram F; Onay H; Özgür S; Mcintyre AD; Toth PP; Hegele RA
Turk Kardiyol Dern Ars; 2023 Jan; 51(1):10-21. PubMed ID: 36689289
[TBL] [Abstract][Full Text] [Related]
13. Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia.
Cefalù AB; Noto D; Arpi ML; Yin F; Spina R; Hilden H; Barbagallo CM; Carroccio A; Tarugi P; Squatrito S; Vigneri R; Taskinen MR; Péterfy M; Averna MR
J Clin Endocrinol Metab; 2009 Nov; 94(11):4584-90. PubMed ID: 19820022
[TBL] [Abstract][Full Text] [Related]
14. Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia.
Surendran RP; Visser ME; Heemelaar S; Wang J; Peter J; Defesche JC; Kuivenhoven JA; Hosseini M; Péterfy M; Kastelein JJ; Johansen CT; Hegele RA; Stroes ES; Dallinga-Thie GM
J Intern Med; 2012 Aug; 272(2):185-96. PubMed ID: 22239554
[TBL] [Abstract][Full Text] [Related]
15. Characterization of two novel pathogenic variants at compound heterozygous status in lipase maturation factor 1 gene causing severe hypertriglyceridemia.
Péterfy M; Bedoya C; Giacobbe C; Pagano C; Gentile M; Rubba P; Fortunato G; Di Taranto MD
J Clin Lipidol; 2018; 12(5):1253-1259. PubMed ID: 30172716
[TBL] [Abstract][Full Text] [Related]
16. The polygenic nature of mild-to-moderate hypertriglyceridemia.
Dron JS; Wang J; McIntyre AD; Cao H; Hegele RA
J Clin Lipidol; 2020; 14(1):28-34.e2. PubMed ID: 32033914
[TBL] [Abstract][Full Text] [Related]
17. New rare genetic variants of LMF1 gene identified in severe hypertriglyceridemia.
Serveaux Dancer M; Di Filippo M; Marmontel O; Valéro R; Piombo Rivarola MDC; Peretti N; Caussy C; Krempf M; Vergès B; Mahl M; Marçais C; Moulin P; Charrière S
J Clin Lipidol; 2018; 12(5):1244-1252. PubMed ID: 30037590
[TBL] [Abstract][Full Text] [Related]
18. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
[TBL] [Abstract][Full Text] [Related]
19. Rare genetic variants with large effect on triglycerides in subjects with a clinical diagnosis of familial vs nonfamilial hypertriglyceridemia.
De Castro-Orós I; Civeira F; Pueyo MJ; Mateo-Gallego R; Bolado-Carrancio A; Lamíquiz-Moneo I; Álvarez-Sala L; Fabiani F; Cofán M; Cenarro A; Rodríguez-Rey JC; Ros E; Pocoví M
J Clin Lipidol; 2016; 10(4):790-797. PubMed ID: 27578109
[TBL] [Abstract][Full Text] [Related]
20. Identification of a novel LPL nonsense variant and further insights into the complex etiology and expression of hypertriglyceridemia-induced acute pancreatitis.
Li XY; Pu N; Chen WW; Shi XL; Zhang GF; Ke L; Ye B; Tong ZH; Wang YH; Liu G; Chen JM; Yang Q; Li WQ; Li JS
Lipids Health Dis; 2020 Apr; 19(1):63. PubMed ID: 32264896
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
