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Liver disease related to alpha1-antitrypsin deficiency in French children: The DEFI-ALPHA cohort.
Ruiz M, Lacaille F, Berthiller J, Joly P, Dumortier J, Aumar M, Bridoux-Henno L, Jacquemin E, Lamireau T, Broué P, Rivet C, Belmalih A, Restier L, Chapuis-Cellier C, Bouchecareilh M, Lachaux A; Groupe Francophone d’Hépatologie Gastroentérologie et Nutrition Pédiatriques. Ruiz M, et al. Among authors: restier l. Liver Int. 2019 Jun;39(6):1136-1146. doi: 10.1111/liv.14035. Epub 2019 Feb 1. Liver Int. 2019. PMID: 30589493
ERAD defects and the HFE-H63D variant are associated with increased risk of liver damages in Alpha 1-Antitrypsin Deficiency.
Joly P, Vignaud H, Di Martino J, Ruiz M, Garin R, Restier L, Belmalih A, Marchal C, Cullin C, Arveiler B, Fergelot P, Gitler AD, Lachaux A, Couthouis J, Bouchecareilh M. Joly P, et al. Among authors: restier l. PLoS One. 2017 Jun 15;12(6):e0179369. doi: 10.1371/journal.pone.0179369. eCollection 2017. PLoS One. 2017. PMID: 28617828 Free PMC article.
[DEFI-ALPHA cohort and POLYGEN DEFI-ALPHA clinical research hospital programme. A study about clinical, biological and genetics factors associated with the occurrence and the evolution of hepatic complications in children with alpha-1 antitrypsin deficiency].
Joly P, Restier L, Bouchecareilh M, Lacan P, Cabet F, Chapuis-Cellier C, Francina A, Lachaux A. Joly P, et al. Among authors: restier l. Rev Mal Respir. 2015 Sep;32(7):759-67. doi: 10.1016/j.rmr.2015.06.010. Epub 2015 Aug 1. Rev Mal Respir. 2015. PMID: 26238925 French.
Paediatric liver transplanted patients and prevalence of hepatitis E virus.
Laverdure N, Scholtès-Brunel C, Rivet C, Heissat S, Restier L, Bacchetta J, Boillot O, Dumortier J, Lachaux A. Laverdure N, et al. Among authors: restier l. J Clin Virol. 2015 Aug;69:22-6. doi: 10.1016/j.jcv.2015.04.022. Epub 2015 May 19. J Clin Virol. 2015. PMID: 26209371
Establishment of reference values of α-tocopherol in plasma, red blood cells and adipose tissue in healthy children to improve the management of chylomicron retention disease, a rare genetic hypocholesterolemia.
Cuerq C, Restier L, Drai J, Blond E, Roux A, Charriere S, Michalski MC, Di Filippo M, Levy E, Lachaux A, Peretti N. Cuerq C, et al. Among authors: restier l. Orphanet J Rare Dis. 2016 Aug 12;11(1):114. doi: 10.1186/s13023-016-0498-8. Orphanet J Rare Dis. 2016. PMID: 27520363 Free PMC article.
A prospective case-control pilot study to evaluate bone microarchitecture in children and teenagers on long-term parenteral nutrition using HR-pQCT.
Louazon T, Poinsot P, Restier L, Belmalih A, Loras-Duclaux I, Marotte S, Heissat S, Barnoud D, Chambrier C, Confavreux CB, Lachaux A, Bacchetta J, Peretti N. Louazon T, et al. Among authors: restier l. Sci Rep. 2021 Apr 28;11(1):9151. doi: 10.1038/s41598-021-88366-6. Sci Rep. 2021. PMID: 33911128 Free PMC article.
24 results