Sassolas A - Search Results

1

Efficacy of two vitamin E formulations in patients with abetalipoproteinemia and chylomicron retention disease.

Cuerq C, Henin E, Restier L, Blond E, Drai J, Marçais C, Di Filippo M, Laveille C, Michalski MC, Poinsot P, Caussy C, Sassolas A, Moulin P, Reboul E, Charriere S, Levy E, Lachaux A, Peretti N. Cuerq C, et al. Among authors: sassolas a. J Lipid Res. 2018 Sep;59(9):1640-1648. doi: 10.1194/jlr.M085043. Epub 2018 Jul 18. J Lipid Res. 2018. PMID: 30021760 Free PMC article.

2

Digestive tract involvement in an infant and a child with Tangier disease.

Lachaux A, Sassolas A, Loras-Duclaux I, Le Gall C, Bouvier R. Lachaux A, et al. Among authors: sassolas a. J Pediatr Gastroenterol Nutr. 1998 Aug;27(2):234-6. doi: 10.1097/00005176-199808000-00022. J Pediatr Gastroenterol Nutr. 1998. PMID: 9702662 No abstract available.

3

Alteration in lipoprotein lipase activity bound to triglyceride-rich lipoproteins in the postprandial state in type 2 diabetes.

Pruneta-Deloche V, Sassolas A, Dallinga-Thie GM, Berthezène F, Ponsin G, Moulin P. Pruneta-Deloche V, et al. Among authors: sassolas a. J Lipid Res. 2004 May;45(5):859-65. doi: 10.1194/jlr.M300435-JLR200. Epub 2004 Feb 16. J Lipid Res. 2004. PMID: 14967813 Free article.

4

Relation between XbA1 apolipoprotein B gene polymorphism and cardiovascular risk in a type 2 diabetic cohort.

Bernard S, Charrière S, Charcosset M, Berthezène F, Moulin P, Sassolas A. Bernard S, et al. Among authors: sassolas a. Atherosclerosis. 2004 Jul;175(1):177-81. doi: 10.1016/j.atherosclerosis.2004.03.017. Atherosclerosis. 2004. PMID: 15186963

5

Combination of circulating antilipoprotein lipase (Anti-LPL) antibody and heterozygous S172 fsX179 mutation of LPL gene leading to chronic hyperchylomicronemia.

Pruneta-Deloche V, Marçais C, Perrot L, Sassolas A, Delay M, Estour B, Lagarde M, Moulin P. Pruneta-Deloche V, et al. Among authors: sassolas a. J Clin Endocrinol Metab. 2005 Jul;90(7):3995-8. doi: 10.1210/jc.2005-0205. Epub 2005 Apr 19. J Clin Endocrinol Metab. 2005. PMID: 15840743

6

Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment.

Marçais C, Verges B, Charrière S, Pruneta V, Merlin M, Billon S, Perrot L, Drai J, Sassolas A, Pennacchio LA, Fruchart-Najib J, Fruchart JC, Durlach V, Moulin P. Marçais C, et al. Among authors: sassolas a. J Clin Invest. 2005 Oct;115(10):2862-9. doi: 10.1172/JCI24471. J Clin Invest. 2005. PMID: 16200213 Free PMC article.

7

Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein.

Charcosset M, Sassolas A, Peretti N, Roy CC, Deslandres C, Sinnett D, Levy E, Lachaux A. Charcosset M, et al. Among authors: sassolas a. Mol Genet Metab. 2008 Jan;93(1):74-84. doi: 10.1016/j.ymgme.2007.08.120. Epub 2007 Oct 22. Mol Genet Metab. 2008. PMID: 17945526

8

Association of APOA5 -1131T>C and S19W gene polymorphisms with both mild hypertriglyceridemia and hyperchylomicronemia in type 2 diabetic patients.

Charriere S, Bernard S, Aqallal M, Merlin M, Billon S, Perrot L, Le Coquil E, Sassolas A, Moulin P, Marcais C. Charriere S, et al. Among authors: sassolas a. Clin Chim Acta. 2008 Aug;394(1-2):99-103. doi: 10.1016/j.cca.2008.04.013. Epub 2008 Apr 27. Clin Chim Acta. 2008. PMID: 18468520

9

Identification of two novel mutations and long-term follow-up in abetalipoproteinemia: a report of four cases.

Chardon L, Sassolas A, Dingeon B, Michel-Calemard L, Bovier-Lapierre M, Moulin P, Lachaux A. Chardon L, et al. Among authors: sassolas a. Eur J Pediatr. 2009 Aug;168(8):983-9. doi: 10.1007/s00431-008-0888-6. Epub 2008 Dec 9. Eur J Pediatr. 2009. PMID: 19066957

10

Chylomicron retention disease: a long term study of two cohorts.

Peretti N, Roy CC, Sassolas A, Deslandres C, Drouin E, Rasquin A, Seidman E, Brochu P, Vohl MC, Labarge S, Bouvier R, Samson-Bouma ME, Charcosset M, Lachaux A, Levy E. Peretti N, et al. Among authors: sassolas a. Mol Genet Metab. 2009 Jun;97(2):136-42. doi: 10.1016/j.ymgme.2009.02.003. Epub 2009 Feb 20. Mol Genet Metab. 2009. PMID: 19285442

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