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Initial presentation, management and follow-up data of 33 treated patients with hereditary tyrosinemia type 1 in the absence of newborn screening.
Hajji H, Imbard A, Spraul A, Taibi L, Barbier V, Habes D, Brassier A, Arnoux JB, Bouchereau J, Pichard S, Sissaoui S, Lacaille F, Girard M, Debray D, de Lonlay P, Schiff M. Hajji H, et al. Among authors: lacaille f. Mol Genet Metab Rep. 2022 Nov 8;33:100933. doi: 10.1016/j.ymgmr.2022.100933. eCollection 2022 Dec. Mol Genet Metab Rep. 2022. PMID: 36393896 Free PMC article.
Development of liver disease despite mannose treatment in two patients with CDG-Ib.
Mention K, Lacaille F, Valayannopoulos V, Romano S, Kuster A, Cretz M, Zaidan H, Galmiche L, Jaubert F, de Keyzer Y, Seta N, de Lonlay P. Mention K, et al. Among authors: lacaille f. Mol Genet Metab. 2008 Jan;93(1):40-3. doi: 10.1016/j.ymgme.2007.08.126. Epub 2007 Oct 22. Mol Genet Metab. 2008. PMID: 17945525
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
Specificities of sclerosing cholangitis in childhood.
Girard M, Franchi-Abella S, Lacaille F, Debray D. Girard M, et al. Among authors: lacaille f. Clin Res Hepatol Gastroenterol. 2012 Dec;36(6):530-5. doi: 10.1016/j.clinre.2012.04.003. Epub 2012 May 23. Clin Res Hepatol Gastroenterol. 2012. PMID: 22633198 Review.
Dihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome.
Brassier A, Ottolenghi C, Boutron A, Bertrand AM, Valmary-Degano S, Cervoni JP, Chrétien D, Arnoux JB, Hubert L, Rabier D, Lacaille F, de Keyzer Y, Di Martino V, de Lonlay P. Brassier A, et al. Among authors: lacaille f. Mol Genet Metab. 2013 May;109(1):28-32. doi: 10.1016/j.ymgme.2013.01.017. Epub 2013 Feb 1. Mol Genet Metab. 2013. PMID: 23478190
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
Early and late complications after liver transplantation for propionic acidemia in children: a two centers study.
Charbit-Henrion F, Lacaille F, McKiernan P, Girard M, de Lonlay P, Valayannopoulos V, Ottolenghi C, Chakrapani A, Preece M, Sharif K, Chardot C, Hubert P, Dupic L. Charbit-Henrion F, et al. Among authors: lacaille f. Am J Transplant. 2015 Mar;15(3):786-91. doi: 10.1111/ajt.13027. Epub 2015 Feb 12. Am J Transplant. 2015. PMID: 25683683 Free article.
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