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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
2007 1
2008 2
2009 1
2014 2
2016 1
2017 6
2018 6
2019 2
2020 2
2021 4
2024 0

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Page 1
Trichohepatoenteric Syndrome.
Fabre A, Bourgeois P, Chaix C, Bertaux K, Goulet O, Badens C. Fabre A, et al. Among authors: bourgeois p. 2018 Jan 11. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2018 Jan 11. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 29334452 Free Books & Documents. Review.
Combined Immunodeficiency in Patients With Trichohepatoenteric Syndrome.
Vély F, Barlogis V, Marinier E, Coste ME, Dubern B, Dugelay E, Lemale J, Martinez-Vinson C, Peretti N, Perry A, Bourgeois P, Badens C, Goulet O, Hugot JP, Farnarier C, Fabre A. Vély F, et al. Among authors: bourgeois p. Front Immunol. 2018 May 11;9:1036. doi: 10.3389/fimmu.2018.01036. eCollection 2018. Front Immunol. 2018. PMID: 29868001 Free PMC article.
IBD-Like Features in Syndromic Diarrhea/Trichohepatoenteric Syndrome.
Busoni VB, Lemale J, Dubern B, Frangi F, Bourgeois P, Orsi M, Badens C, Fabre A. Busoni VB, et al. Among authors: bourgeois p. J Pediatr Gastroenterol Nutr. 2017 Jan;64(1):37-41. doi: 10.1097/MPG.0000000000001218. J Pediatr Gastroenterol Nutr. 2017. PMID: 28027214
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. Among authors: bourgeois p. 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
25 results