These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 9350308)

  • 41. Severe hypertriglyceridemia in an infant of Arab descent.
    Behar DM; Adler L; Basel-Vanagaite L
    Isr Med Assoc J; 2013 Jan; 15(1):53-4. PubMed ID: 23484243
    [No Abstract]   [Full Text] [Related]  

  • 42. Lipoprotein lipase deficiency in an infant.
    Nampoothiri S; Radhakrishnan N; Schwentek A; Hoffmann MM
    Indian Pediatr; 2011 Oct; 48(10):805-6. PubMed ID: 22080683
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia.
    Pingitore P; Lepore SM; Pirazzi C; Mancina RM; Motta BM; Valenti L; Berge KE; Retterstøl K; Leren TP; Wiklund O; Romeo S
    J Clin Lipidol; 2016; 10(4):816-823. PubMed ID: 27578112
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians.
    Ma Y; Henderson HE; Murthy V; Roederer G; Monsalve MV; Clarke LA; Normand T; Julien P; Gagné C; Lambert M
    N Engl J Med; 1991 Jun; 324(25):1761-6. PubMed ID: 2038366
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Homozygous LPL p.Gly188Glu Mutation in a Mexican Girl With Lipoprotein Lipase Deficiency.
    Colima Fausto AG; González García JR; Hernández Flores TJ; Vázquez Cárdenas NA; Solís Perales NE; Magaña Torres MT
    Ann Lab Med; 2017 Jul; 37(4):355-358. PubMed ID: 28445021
    [No Abstract]   [Full Text] [Related]  

  • 47. Primary type 1 hyperlipoproteinemia: significance of lipoprotein lipase and hepatic triglyceride lipase activity in heterozygotes of patients with familial lipoprotein lipase deficiency.
    Go T; Ohkubo H; Mochizuki Y; Murase T; Yamada N
    J Pediatr; 1983 Mar; 102(3):405-7. PubMed ID: 6827414
    [No Abstract]   [Full Text] [Related]  

  • 48. Homozygous LPL and GPIHBP1 variants causing familial chylomicronaemia syndrome in Sri Lankan children.
    Kiyamudeen F; Rajapaksha M; Atapattu N; Kularatne SD; Schröder S; Hooper AJ; Burnett JR; Jasinge E
    Pathology; 2024 Oct; 56(6):904-906. PubMed ID: 38777740
    [No Abstract]   [Full Text] [Related]  

  • 49. Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase gene.
    Benlian P; De Gennes JL; Foubert L; Zhang H; Gagné SE; Hayden M
    N Engl J Med; 1996 Sep; 335(12):848-54. PubMed ID: 8778602
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene.
    Hata A; Emi M; Luc G; Basdevant A; Gambert P; Iverius PH; Lalouel JM
    Am J Hum Genet; 1990 Oct; 47(4):721-6. PubMed ID: 2121025
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A novel substitution at the translation initiator codon (ATG-->ATC) of the lipoprotein lipase gene is mainly responsible for lipoprotein lipase deficiency in a patient with severe hypertriglyceridemia and recurrent pancreatitis.
    Yu XH; Zhao TQ; Wang L; Liu ZP; Zhang CM; Chen R; Li L; Liu G; Hu WC
    Biochem Biophys Res Commun; 2006 Mar; 341(1):82-7. PubMed ID: 16431216
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The role of registries in rare genetic lipid disorders: Review and introduction of the first global registry in lipoprotein lipase deficiency.
    Steinhagen-Thiessen E; Stroes E; Soran H; Johnson C; Moulin P; Iotti G; Zibellini M; Ossenkoppele B; Dippel M; Averna MR;
    Atherosclerosis; 2017 Jul; 262():146-153. PubMed ID: 28284702
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Intramuscular administration of AAV1-lipoprotein lipase S447X lowers triglycerides in lipoprotein lipase-deficient patients.
    Stroes ES; Nierman MC; Meulenberg JJ; Franssen R; Twisk J; Henny CP; Maas MM; Zwinderman AH; Ross C; Aronica E; High KA; Levi MM; Hayden MR; Kastelein JJ; Kuivenhoven JA
    Arterioscler Thromb Vasc Biol; 2008 Dec; 28(12):2303-4. PubMed ID: 18802015
    [No Abstract]   [Full Text] [Related]  

  • 54. Gene therapy for genetic lipid disorders: lipoprotein lipase deficiency as a paradigm.
    Rader DJ
    Neth J Med; 2005 Jan; 63(1):2-3. PubMed ID: 15719845
    [No Abstract]   [Full Text] [Related]  

  • 55. Compound heterozygosity for frameshift mutations in the gene for lipoprotein lipase in a patient with early-onset chylomicronemia.
    Foubert L; De Gennes JL; Benlian P; Truffert J; Miao L; Hayden MR
    Hum Mutat; 1998; Suppl 1():S141-4. PubMed ID: 9452069
    [No Abstract]   [Full Text] [Related]  

  • 56. [A case of neonatal lipoprotein lipase deficiency caused by novel compound heterozygous variants of LPL gene].
    Zhu L; Li G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Feb; 37(2):156-158. PubMed ID: 32034744
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiency.
    Henderson HE; Devlin R; Peterson J; Brunzell JD; Hayden MR
    Mol Biol Med; 1990 Dec; 7(6):511-7. PubMed ID: 2077351
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genotype-phenotype relationships in patients with type I hyperlipoproteinemia.
    Chokshi N; Blumenschein SD; Ahmad Z; Garg A
    J Clin Lipidol; 2014; 8(3):287-95. PubMed ID: 24793350
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Abnormal lipoprotein level and the genetic analysis].
    Gotoda T; Yamada N
    Nihon Naika Gakkai Zasshi; 1992 Nov; 81(11):1825-30. PubMed ID: 1479225
    [No Abstract]   [Full Text] [Related]  

  • 60. Adipose tissue fatty acid composition in humans with lipoprotein lipase deficiency.
    Ullrich NF; Purnell JQ; Brunzell JD
    J Investig Med; 2001 May; 49(3):273-5. PubMed ID: 11352185
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.