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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: lacaille f. Liver Int. 2019 Jun;39(6):1136-1146. doi: 10.1111/liv.14035. Epub 2019 Feb 1. Liver Int. 2019. PMID: 30589493
Apolipoprotein B Arg3500Gln mutation prevalence in children with hypercholesterolemia: a French multicenter study.
Viola S, Benlian P, Morali A, Dobbelaere D, Lacaille F, Rieu D, Ginies JL, Maurage C, Meyer M, Lachaux A, Larchet M, Lenearts C, Goulet O, Sarles J, Mouterde O, Girardet JP; French-Speaking Group for Pediatric Hepatogastroenterology and Nutrition. Viola S, et al. Among authors: lacaille f. J Pediatr Gastroenterol Nutr. 2001 Aug;33(2):122-6. doi: 10.1097/00005176-200108000-00005. J Pediatr Gastroenterol Nutr. 2001. PMID: 11568510
AIRE gene analysis in children with autoimmune hepatitis type I or II.
Lankisch TO, Mourier O, Sokal EM, Habes D, Lacaille F, Bridoux-Henno L, Hermeziu B, Lenaerts C, Strassburg CP, Jacquemin E. Lankisch TO, et al. Among authors: lacaille f. J Pediatr Gastroenterol Nutr. 2009 Apr;48(4):498-500. doi: 10.1097/MPG.0b013e31818550de. J Pediatr Gastroenterol Nutr. 2009. PMID: 19322061
De novo malignancy after solid organ transplantation in children.
Debray D, Baudouin V, Lacaille F, Charbit M, Rivet C, Harambat J, Iserin F, Di Filippo S, Guyot C; Pediatric Transplantation Working Group of the French Speaking Society of Transplantation. Debray D, et al. Among authors: lacaille f. Transplant Proc. 2009 Mar;41(2):674-5. doi: 10.1016/j.transproceed.2008.12.020. Transplant Proc. 2009. PMID: 19328954
Other genetic liver diseases in children.
Lacaille F. Lacaille F. Clin Res Hepatol Gastroenterol. 2012 Jun;36(3):301-3. doi: 10.1016/j.clinre.2012.03.027. Epub 2012 Apr 25. Clin Res Hepatol Gastroenterol. 2012. PMID: 22541062
MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease.
Girard M, Lacaille F, Verkarre V, Mategot R, Feldmann G, Grodet A, Sauvat F, Irtan S, Davit-Spraul A, Jacquemin E, Ruemmele F, Rainteau D, Goulet O, Colomb V, Chardot C, Henrion-Caude A, Debray D. Girard M, et al. Among authors: lacaille f. Hepatology. 2014 Jul;60(1):301-10. doi: 10.1002/hep.26974. Epub 2014 May 27. Hepatology. 2014. PMID: 24375397
Severe chronic primary neutropenia in adults: report on a series of 108 patients.
Sicre de Fontbrune F, Moignet A, Beaupain B, Suarez F, Galicier L, Socié G, Varet B, Coppo P, Michel M, Pautas C, Oksenhendler E, Lengline E, Terriou L, Moreau P, Chantepie S, Casadevall N, Michot JM, Gardembas M, Michallet M, Croisille L, Audrain M, Bellanné-Chantelot C, Donadieu J, Lamy T; French Severe Chronic Neutropenia Registry. Sicre de Fontbrune F, et al. Blood. 2015 Oct 1;126(14):1643-50. doi: 10.1182/blood-2015-03-634493. Epub 2015 Aug 10. Blood. 2015. PMID: 26261239 Free article.
230 results