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Year Number of Results
1981 1
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1987 1
1988 1
1989 14
1990 15
1991 1
1992 1
1999 1
2001 1
2005 1
2006 1
2007 1
2008 3
2009 2
2010 3
2011 2
2012 4
2013 3
2014 5
2015 2
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2017 3
2018 4
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2021 5
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2024 1

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90 results

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Page 1
Genetic Diagnosis Guides Treatment of Autoimmune Enteropathy.
Charbit-Henrion F, Haas M, Chaussade S, Cellier C, Cerf-Bensussan N, Malamut G; Contributors from the AUTOIMMUNE ENTEROPATHY WORKING GROUP; Khater S, Khiat A, Cording S, Parlato M, Dragon-Durey MA, Beuvon F, Brousse N, Terris B, Picard C, Fusaro M, Rieux-Laucat F, Stolzenberg MC, Jannot AS, Mathian A, Allez M, Malphettes M, Fieschi C, Aubourg A, Zallot C, Roblin X, Abitbol V, Belle A, Wils P, Cheminant M, Matysiak-Budnik T, Vuitton L, Pouderoux P, Abramowitz L, Castelle M, Suarez F, Hermine O, Ruemmele F, Mouthon L. Charbit-Henrion F, et al. Among authors: parlato m. Clin Gastroenterol Hepatol. 2023 May;21(5):1368-1371.e2. doi: 10.1016/j.cgh.2022.07.030. Epub 2022 Aug 6. Clin Gastroenterol Hepatol. 2023. PMID: 35944833 Free PMC article. No abstract available.
Insights into the expanding intestinal phenotypic spectrum of SOCS1 haploinsufficiency and therapeutic options.
Rodari MM, Cazals-Hatem D, Uzzan M, Martin Silva N, Khiat A, Ta MC, Lhermitte L, Touzart A, Hanein S, Rouillon C, Joly F, Elmorjani A, Steffann J, Cerf-Bensussan N, Parlato M, Charbit-Henrion F. Rodari MM, et al. Among authors: parlato m. J Clin Immunol. 2023 Aug;43(6):1403-1413. doi: 10.1007/s10875-023-01495-7. Epub 2023 May 9. J Clin Immunol. 2023. PMID: 37156989 Free PMC article.
Intestinal immunoregulation: lessons from human mendelian diseases.
Charbit-Henrion F, Parlato M, Malamut G, Ruemmele F, Cerf-Bensussan N. Charbit-Henrion F, et al. Among authors: parlato m. Mucosal Immunol. 2021 Sep;14(5):1017-1037. doi: 10.1038/s41385-021-00398-3. Epub 2021 Apr 15. Mucosal Immunol. 2021. PMID: 33859369 Free article. Review.
Dysregulation of the immune response in TGF-β signalopathies.
Rodari MM, Cerf-Bensussan N, Parlato M. Rodari MM, et al. Among authors: parlato m. Front Immunol. 2022 Dec 9;13:1066375. doi: 10.3389/fimmu.2022.1066375. eCollection 2022. Front Immunol. 2022. PMID: 36569843 Free PMC article. Review.
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
Duclaux-Loras R, Lebreton C, Berthelet J, Charbit-Henrion F, Nicolle O, Revenu des Courtils C, Waich S, Valovka T, Khiat A, Rabant M, Racine C, Guerrera IC, Baptista J, Mahe MM, Hess MW, Durel B, Lefort N, Banal C, Parisot M, Talbotec C, Lacaille F, Ecochard-Dugelay E, Demir AM, Vogel GF, Faivre L, Rodrigues A, Fowler D, Janecke AR, Müller T, Huber LA, Rodrigues-Lima F, Ruemmele FM, Uhlig HH, Del Bene F, Michaux G, Cerf-Bensussan N, Parlato M. Duclaux-Loras R, et al. Among authors: parlato m. J Clin Invest. 2022 May 16;132(10):e154997. doi: 10.1172/JCI154997. J Clin Invest. 2022. PMID: 35575086 Free PMC article.
Systemic inflammatory syndrome in children with FARSA deficiency.
Charbit-Henrion F, Goguyer-Deschaumes R, Borensztajn K, Mirande M, Berthelet J, Rodrigues-Lima F, Khiat A, Frémond ML, Bader-Meunier B, Rodari MM, Seabra L, Rice GI, Legendre M, Drummond D, Berteloot L, Roux CJ, Boddaert N, Drabent P, Molina TJ, Lacaille F, Kossorotoff M, Cerf-Bensussan N, Parlato M, Hadchouel A. Charbit-Henrion F, et al. Among authors: parlato m. Clin Genet. 2022 May;101(5-6):552-558. doi: 10.1111/cge.14120. Epub 2022 Feb 17. Clin Genet. 2022. PMID: 35132614 Free PMC article.
90 results