Levy E - Search Results

1

Reduced brain choline in homocystinuria due to remethylation defects.

Debray FG, Boulanger Y, Khiat A, Decarie JC, Orquin J, Roy MS, Lortie A, Ramos F, Verhoeven NM, Struys E, Blom HJ, Jakobs C, Levy E, Mitchell GA, Lambert M. Debray FG, et al. Among authors: levy e. Neurology. 2008 Jul 1;71(1):44-9. doi: 10.1212/01.wnl.0000316391.40236.c3. Neurology. 2008. PMID: 18591504 Free article.

2

Mechanisms of hypercholesterolaemia in glycogen storage disease type I: defective metabolism of low density lipoprotein in cultured skin fibroblasts.

Levy E, Thibault L, Roy CC, Letarte J, Lambert M, Seidman EG. Levy E, et al. Eur J Clin Invest. 1990 Jun;20(3):253-60. doi: 10.1111/j.1365-2362.1990.tb01852.x. Eur J Clin Invest. 1990. PMID: 2114985

3

Familial hypercholesterolemia: molecular, biochemical, and clinical characterization of a French-Canadian pediatric population.

Assouline L, Levy E, Feoli-Fonseca JC, Godbout C, Lambert M. Assouline L, et al. Among authors: levy e. Pediatrics. 1995 Aug;96(2 Pt 1):239-46. Pediatrics. 1995. PMID: 7630677

4

Lipoprotein abnormalities in two children with minimal biliary excretion.

Levy E, Bendayan M, Thibault L, Lambert M, Paradis K. Levy E, et al. J Pediatr Gastroenterol Nutr. 1995 May;20(4):432-9. doi: 10.1097/00005176-199505000-00009. J Pediatr Gastroenterol Nutr. 1995. PMID: 7636686 No abstract available.

5

Lipoprotein abnormalities associated with cholesteryl ester transfer activity in cystic fibrosis patients: the role of essential fatty acid deficiency.

Lévy E, Roy C, Lacaille F, Lambert M, Messier M, Gavino V, Lepage G, Thibault L. Lévy E, et al. Am J Clin Nutr. 1993 Apr;57(4):573-9. doi: 10.1093/ajcn/57.4.573. Am J Clin Nutr. 1993. PMID: 8460614

6

Association of an exon 3 mutation (Trp66-->Gly) of the LDL receptor with variable expression of familial hypercholesterolemia in a French Canadian family.

Levy E, Minnich A, Cacan SL, Thibault L, Giroux LM, Davignon J, Lambert M. Levy E, et al. Biochem Mol Med. 1997 Feb;60(1):59-69. doi: 10.1006/bmme.1996.2549. Biochem Mol Med. 1997. PMID: 9066982

7

Identification of two novel LDL receptor gene defects in French-Canadian pediatric population: mutational analysis and biochemical studies.

Assouline L, Leitersdorf E, Lambert M, Reshef A, Feoli-Fonseca JC, Levy E. Assouline L, et al. Among authors: levy e. Hum Mutat. 1997;9(6):555-62. doi: 10.1002/(SICI)1098-1004(1997)9:6<555::AID-HUMU9>3.0.CO;2-0. Hum Mutat. 1997. PMID: 9195230

8

Familial lipoprotein lipase deficiency in infancy: clinical, biochemical, and molecular study.

Feoli-Fonseca JC, Lévy E, Godard M, Lambert M. Feoli-Fonseca JC, et al. Among authors: levy e. J Pediatr. 1998 Sep;133(3):417-23. doi: 10.1016/s0022-3476(98)70280-x. J Pediatr. 1998. PMID: 9738727

9

The adipose tissue phenotype of hormone-sensitive lipase deficiency in mice.

Wang SP, Laurin N, Himms-Hagen J, Rudnicki MA, Levy E, Robert MF, Pan L, Oligny L, Mitchell GA. Wang SP, et al. Among authors: levy e. Obes Res. 2001 Feb;9(2):119-28. doi: 10.1038/oby.2001.15. Obes Res. 2001. PMID: 11316346 Free article.

10

Determinants of lipid level variability in French-Canadian children with familial hypercholesterolemia.

Lambert M, Assouline L, Feoli-Fonseca JC, Brun N, Delvin EE, Lévy E. Lambert M, et al. Among authors: levy e. Arterioscler Thromb Vasc Biol. 2001 Jun;21(6):979-84. doi: 10.1161/01.atv.21.6.979. Arterioscler Thromb Vasc Biol. 2001. PMID: 11397707

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