276 related articles for article (PubMed ID: 26337181)
1. Severe Hypertriglyceridemia due to a novel p.Q240H mutation in the Lipoprotein Lipase gene.
Soto AG; McIntyre A; Agrawal S; Bialo SR; Hegele RA; Boney CM
Lipids Health Dis; 2015 Sep; 14():102. PubMed ID: 26337181
[TBL] [Abstract][Full Text] [Related]
2. Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants.
Kassner U; Salewsky B; Wühle-Demuth M; Szijarto IA; Grenkowitz T; Binner P; März W; Steinhagen-Thiessen E; Demuth I
Eur J Hum Genet; 2015 Sep; 23(9):1259-61. PubMed ID: 25585702
[TBL] [Abstract][Full Text] [Related]
3. Novel LPL mutations associated with lipoprotein lipase deficiency: two case reports and a literature review.
Rahalkar AR; Giffen F; Har B; Ho J; Morrison KM; Hill J; Wang J; Hegele RA; Joy T
Can J Physiol Pharmacol; 2009 Mar; 87(3):151-60. PubMed ID: 19295657
[TBL] [Abstract][Full Text] [Related]
4. Two novel mutations in the lipoprotein lipase gene in a family with marked hypertriglyceridemia in heterozygous carriers. Potential interaction with the polymorphic marker D1S104 on chromosome 1q21-q23.
Hölzl B; Kraft HG; Wiebusch H; Sandhofer A; Patsch J; Sandhofer F; Paulweber B
J Lipid Res; 2000 May; 41(5):734-41. PubMed ID: 10787434
[TBL] [Abstract][Full Text] [Related]
5. Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice. Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotes.
Weinstock PH; Bisgaier CL; Aalto-Setälä K; Radner H; Ramakrishnan R; Levak-Frank S; Essenburg AD; Zechner R; Breslow JL
J Clin Invest; 1995 Dec; 96(6):2555-68. PubMed ID: 8675619
[TBL] [Abstract][Full Text] [Related]
6. Diagnosis and treatment of severe hypertriglyceridemia.
Viljoen A; Wierzbicki AS
Expert Rev Cardiovasc Ther; 2012 Apr; 10(4):505-14. PubMed ID: 22458582
[TBL] [Abstract][Full Text] [Related]
7. Compound heterozygosity of Leu252Val and Leu252Arg causing lipoprotein lipase deficiency in a chinese patient with hypertriglyceridemia.
Chan L; Mak Y; Tomlinson B; Baum L; Wu X; Masarei J; Pang C
Eur J Clin Invest; 2000 Jan; 30(1):33-40. PubMed ID: 10619999
[TBL] [Abstract][Full Text] [Related]
8. Molecular screening of the lipoprotein lipase gene in hypertriglyceridemic members of familial noninsulin-dependent diabetes mellitus families.
Elbein SC; Yeager C; Kwong LK; Lingam A; Inoue I; Lalouel JM; Wilson DE
J Clin Endocrinol Metab; 1994 Nov; 79(5):1450-6. PubMed ID: 7962342
[TBL] [Abstract][Full Text] [Related]
9. Mutations in exon 3 of the lipoprotein lipase gene segregating in a family with hypertriglyceridemia, pancreatitis, and non-insulin-dependent diabetes.
Wilson DE; Hata A; Kwong LK; Lingam A; Shuhua J; Ridinger DN; Yeager C; Kaltenborn KC; Iverius PH; Lalouel JM
J Clin Invest; 1993 Jul; 92(1):203-11. PubMed ID: 8325986
[TBL] [Abstract][Full Text] [Related]
10. A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene.
Buonuomo PS; Bartuli A; Rabacchi C; Bertolini S; Calandra S
J Clin Lipidol; 2015; 9(2):265-70. PubMed ID: 25911085
[TBL] [Abstract][Full Text] [Related]
11. Successful pregnancy outcome in a patient with severe chylomicronemia due to compound heterozygosity for mutant lipoprotein lipase.
Al-Shali K; Wang J; Fellows F; Huff MW; Wolfe BM; Hegele RA
Clin Biochem; 2002 Mar; 35(2):125-30. PubMed ID: 11983347
[TBL] [Abstract][Full Text] [Related]
12. Severe hypertriglyceridemia due to two novel loss-of-function lipoprotein lipase gene mutations (C310R/E396V) in a Chinese family associated with recurrent acute pancreatitis.
Lun Y; Sun X; Wang P; Chi J; Hou X; Wang Y
Oncotarget; 2017 Jul; 8(29):47741-47754. PubMed ID: 28548960
[TBL] [Abstract][Full Text] [Related]
13. Newly identified missense mutation reduces lipoprotein lipase activity in Taiwanese patients with hypertriglyceridemia.
Kao JT; Hsiao WH; Yu CJ; Chiang FT
J Formos Med Assoc; 1999 Sep; 98(9):606-12. PubMed ID: 10560236
[TBL] [Abstract][Full Text] [Related]
14. Familial lipoprotein lipase deficiency: a case of compound heterozygosity of a novel duplication (R44Kfs*4) and a common mutation (N291S) in the lipoprotein lipase gene.
Overgaard M; Brasen CL; Svaneby D; Feddersen S; Nybo M
Ann Clin Biochem; 2013 Jul; 50(Pt 4):374-9. PubMed ID: 23761384
[TBL] [Abstract][Full Text] [Related]
15. Mutations in the lipoprotein lipase gene as a cause of hypertriglyceridemia and pancreatitis in Taiwan.
Jap TS; Jenq SF; Wu YC; Chiu CY; Cheng HM
Pancreas; 2003 Aug; 27(2):122-6. PubMed ID: 12883259
[TBL] [Abstract][Full Text] [Related]
16. 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.
Li X; Yang Q; Shi X; Chen W; Pu N; Li W; Li J
Lipids Health Dis; 2018 Jun; 17(1):144. PubMed ID: 29921298
[TBL] [Abstract][Full Text] [Related]
17. Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia.
Evans D; Arzer J; Aberle J; Beil FU
Atherosclerosis; 2011 Feb; 214(2):386-90. PubMed ID: 21159338
[TBL] [Abstract][Full Text] [Related]
18. A compound heterozygote for a novel missense mutation (G105R) in exon 3 and a missense mutation (D204E) in exon 5 of the lipoprotein lipase gene in a Japanese infant with hyperchylomicronaemia.
Ikeda Y; Goji K; Takagi A
Clin Sci (Lond); 2000 Dec; 99(6):569-78. PubMed ID: 11099402
[TBL] [Abstract][Full Text] [Related]
19. Molecular analysis of three known and one novel LPL variants in patients with type I hyperlipoproteinemia.
Caddeo A; Mancina RM; Pirazzi C; Russo C; Sasidharan K; Sandstedt J; Maurotti S; Montalcini T; Pujia A; Leren TP; Romeo S; Pingitore P
Nutr Metab Cardiovasc Dis; 2018 Feb; 28(2):158-164. PubMed ID: 29288010
[TBL] [Abstract][Full Text] [Related]
20. Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiency.
Bijvoet SM; Wiebusch H; Ma Y; Reymer PW; Bruin T; Bakker HD; Funke H; Assmann G; Hayden MR; Kastelein JJ
Neth J Med; 1996 Nov; 49(5):189-95. PubMed ID: 8973094
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
