L’haploinsuffisance de A20 : que doit connaître le clinicien?-Reference-Cited by-同舟云学术

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L’haploinsuffisance de A20 : que doit connaître le clinicien?

Published:2023-12 Issue: Volume: Page:
ISSN:0248-8663
Container-title:La Revue de Médecine Interne
language:fr
Short-container-title:La Revue de Médecine Interne

Author:

Elhani I.,Aouba A.,Riller Q.,Vergneault H.,Boursier G.,Rieux-Laucat F.,Hentgen V.,Georgin-Lavialle S.

Publisher

Elsevier BV

Subject

Gastroenterology,Internal Medicine

Reference58 articles.

1. A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease;Aeschlimann;Ann Rheum Dis,2018

2. A Japanese family case with juvenile onset Behçet's disease caused by TNFAIP3 mutation;Ohnishi;Allergol Int,2017

3. Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literature;Berteau;Autoimmun Rev,2018

4. Haploinsufficiency of A20 impairs protein-protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation;Rajamäki;RMD Open,2018

5. Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders;Kadowaki;J Allergy Clin Immunol,2018

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Maladies auto-inflammatoires et les déficits immunitaires;Perfectionnement en Pédiatrie;2024-06

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