Peretti N - Search Results

1

GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemia.

Charrière S, Peretti N, Bernard S, Di Filippo M, Sassolas A, Merlin M, Delay M, Debard C, Lefai E, Lachaux A, Moulin P, Marçais C. Charrière S, et al. Among authors: peretti n. J Clin Endocrinol Metab. 2011 Oct;96(10):E1675-9. doi: 10.1210/jc.2011-1444. Epub 2011 Aug 3. J Clin Endocrinol Metab. 2011. PMID: 21816778

2

Microbe-mediated intestinal NOD2 stimulation improves linear growth of undernourished infant mice.

Schwarzer M, Gautam UK, Makki K, Lambert A, Brabec T, Joly A, Šrůtková D, Poinsot P, Novotná T, Geoffroy S, Courtin P, Hermanová PP, Matos RC, Landry JJM, Gérard C, Bulteau AL, Hudcovic T, Kozáková H, Filipp D, Chapot-Chartier MP, Šinkora M, Peretti N, Boneca IG, Chamaillard M, Vidal H, De Vadder F, Leulier F. Schwarzer M, et al. Among authors: peretti n. Science. 2023 Feb 24;379(6634):826-833. doi: 10.1126/science.ade9767. Epub 2023 Feb 23. Science. 2023. PMID: 36821686

3

Cow's milk-based infant formula supplements in breastfed infants and primary prevention of cow's milk allergy: A commentary of the Committee on Nutrition of the French Society of Pediatrics.

Dupont C, Bocquet A, Brancato S, Chalumeau M, Darmaun D, de Luca A, Feillet F, Frelut ML, Guimber D, Lapillonne A, Linglart A, Peretti N, Roze JC, Siméoni U, Turck D, Chouraqui JP; Committee on Nutrition of the French Society of Pediatrics. Dupont C, et al. Among authors: peretti n. Arch Pediatr. 2023 Nov;30(8):591-594. doi: 10.1016/j.arcped.2023.07.005. Epub 2023 Sep 14. Arch Pediatr. 2023. PMID: 37709607

4

The temporal relationship between the onset of type 1 diabetes and celiac disease: a study based on immunoglobulin a antitransglutaminase screening.

Peretti N, Bienvenu F, Bouvet C, Fabien N, Tixier F, Thivolet C, Levy E, Chatelain PG, Lachaux A, Nicolino M. Peretti N, et al. Pediatrics. 2004 May;113(5):e418-22. doi: 10.1542/peds.113.5.e418. Pediatrics. 2004. PMID: 15121983

5

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: peretti n. 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

6

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. 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

7

Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centers.

Peretti N, Sassolas A, Roy CC, Deslandres C, Charcosset M, Castagnetti J, Pugnet-Chardon L, Moulin P, Labarge S, Bouthillier L, Lachaux A, Levy E; Department of Nutrition-Hepatogastroenterology, Hôpital Femme Mère Enfant, Bron, Université Lyon 1; Department of Pediatrics, CHU Sainte-Justine Research Center, Université de Montréal. Peretti N, et al. Orphanet J Rare Dis. 2010 Sep 29;5:24. doi: 10.1186/1750-1172-5-24. Orphanet J Rare Dis. 2010. PMID: 20920215 Free PMC article. Review.

8

Oil composition of high-fat diet affects metabolic inflammation differently in connection with endotoxin receptors in mice.

Laugerette F, Furet JP, Debard C, Daira P, Loizon E, Géloën A, Soulage CO, Simonet C, Lefils-Lacourtablaise J, Bernoud-Hubac N, Bodennec J, Peretti N, Vidal H, Michalski MC. Laugerette F, et al. Among authors: peretti n. Am J Physiol Endocrinol Metab. 2012 Feb 1;302(3):E374-86. doi: 10.1152/ajpendo.00314.2011. Epub 2011 Nov 15. Am J Physiol Endocrinol Metab. 2012. PMID: 22094473 Free article.

9

Inhibitory effects of in vivo oxidized high-density lipoproteins on platelet aggregation: evidence from patients with abetalipoproteinemia.

Calzada C, Véricel E, Colas R, Guillot N, El Khoury G, Drai J, Sassolas A, Peretti N, Ponsin G, Lagarde M, Moulin P. Calzada C, et al. Among authors: peretti n. FASEB J. 2013 Jul;27(7):2855-61. doi: 10.1096/fj.12-225169. Epub 2013 Mar 18. FASEB J. 2013. PMID: 23507868

10

Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia.

Di Filippo M, Moulin P, Roy P, Samson-Bouma ME, Collardeau-Frachon S, Chebel-Dumont S, Peretti N, Dumortier J, Zoulim F, Fontanges T, Parini R, Rigoldi M, Furlan F, Mancini G, Bonnefont-Rousselot D, Bruckert E, Schmitz J, Scoazec JY, Charrière S, Villar-Fimbel S, Gottrand F, Dubern B, Doummar D, Joly F, Liard-Meillon ME, Lachaux A, Sassolas A. Di Filippo M, et al. Among authors: peretti n. J Hepatol. 2014 Oct;61(4):891-902. doi: 10.1016/j.jhep.2014.05.023. Epub 2014 May 16. J Hepatol. 2014. PMID: 24842304

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