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Human inherited complete STAT2 deficiency underlies inflammatory viral diseases.
Bucciol G, Moens L, Ogishi M, Rinchai D, Matuozzo D, Momenilandi M, Kerrouche N, Cale CM, Treffeisen ER, Al Salamah M, Al-Saud BK, Lachaux A, Duclaux-Loras R, Meignien M, Bousfiha A, Benhsaien I, Shcherbina A, Roppelt A; COVID Human Genetic Effort; Gothe F, Houhou-Fidouh N, Hackett SJ, Bartnikas LM, Maciag MC, Alosaimi MF, Chou J, Mohammed RW, Freij BJ, Jouanguy E, Zhang SY, Boisson-Dupuis S, Béziat V, Zhang Q, Duncan CJ, Hambleton S, Casanova JL, Meyts I. Bucciol G, et al. Among authors: duclaux loras r. J Clin Invest. 2023 Jun 15;133(12):e168321. doi: 10.1172/JCI168321. J Clin Invest. 2023. PMID: 36976641 Free PMC article.
A European Survey on Digestive Perianastomotic Ulcerations, a Rare Crohn-like Disorder Occurring in Children and Young Adults.
Madre C, Mašić M, Prlenda-Touilleux D, Brueckner A, Koletzko S, Fabre A, Viala J, Lima R, Enaud R, Lemale J, Kolho KL, Bergoin C, Martinez-Vinson C, Dugelay E, Alvisi P, Aloi M, Miele E, Duclaux-Loras R, Nachury M, Languepin J, Willot S, Dupont-Lucas C, Mosca A, Tzivinikos C, Shamasneh I, Kolaček S, Hugot JP; pediatric GETAID group and the ESPGHAN IBD Porto group. Madre C, et al. J Pediatr Gastroenterol Nutr. 2021 Sep 1;73(3):333-337. doi: 10.1097/MPG.0000000000003200. J Pediatr Gastroenterol Nutr. 2021. PMID: 34117192
Measles virus-imposed remodeling of the autophagy machinery determines the outcome of bacterial coinfection.
Claviere M, Lavedrine A, Lamiral G, Bonnet M, Verlhac P, Petkova DS, Espert L, Duclaux-Loras R, Lucifora J, Rivoire M, Boschetti G, Nancey S, Rozières A, Viret C, Faure M. Claviere M, et al. Among authors: duclaux loras r. Autophagy. 2023 Mar;19(3):858-872. doi: 10.1080/15548627.2022.2107309. Epub 2022 Aug 9. Autophagy. 2023. PMID: 35900944 Free PMC article.
Long-term disease course in a patient with severe neonatal IPEX syndrome.
Duclaux-Loras R, Collardeau-Frachon S, Nancey S, Fabien N, Kaiserlian D, Lachaux A. Duclaux-Loras R, et al. Clin Res Hepatol Gastroenterol. 2015 Sep;39(4):e43-7. doi: 10.1016/j.clinre.2015.03.006. Epub 2015 May 11. Clin Res Hepatol Gastroenterol. 2015. PMID: 25977242
A novel mutation of PCSK1 responsible for PC1/3 deficiency in two siblings.
Duclaux-Loras R, Bourgeois P, Lavrut PM, Charbit-Henrion F, Bonniaud-Blot P, Maudinas R, Bournez M, Faure M, Cerf-Bensussan N, Lachaux A, Peretti N, Fabre A. Duclaux-Loras R, et al. Clin Res Hepatol Gastroenterol. 2021 Nov;45(6):101640. doi: 10.1016/j.clinre.2021.101640. Epub 2021 Mar 1. Clin Res Hepatol Gastroenterol. 2021. PMID: 33662777
36 results