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2. Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease. Tsuchida N; Kirino Y; Soejima Y; Onodera M; Arai K; Tamura E; Ishikawa T; Kawai T; Uchiyama T; Nomura S; Kobayashi D; Taguri M; Mitsuhashi S; Mizuguchi T; Takata A; Miyake N; Nakajima H; Miyatake S; Matsumoto N Arthritis Res Ther; 2019 Jun; 21(1):137. PubMed ID: 31164164 [TBL] [Abstract][Full Text] [Related]
3. Association of Clinical Phenotypes in Haploinsufficiency A20 (HA20) With Disrupted Domains of A20. Chen Y; Ye Z; Chen L; Qin T; Seidler U; Tian D; Xiao F Front Immunol; 2020; 11():574992. PubMed ID: 33101300 [No Abstract] [Full Text] [Related]
4. [Clinical phenotype and immunological features of a patient with A20 haploinsufficiency]. Huang YY; He TY; Xia Y; Luo Y; Weng RH; Luo SL; Yang J; Zhao XD Zhonghua Er Ke Za Zhi; 2020 Mar; 58(3):218-222. PubMed ID: 32135594 [No Abstract] [Full Text] [Related]
5. Haploinsufficiency of A20 Due to Novel Mutations in TNFAIP3. He T; Huang Y; Luo Y; Xia Y; Wang L; Zhang H; Ling J; Yang J J Clin Immunol; 2020 Jul; 40(5):741-751. PubMed ID: 32514655 [TBL] [Abstract][Full Text] [Related]
6. A20 Haploinsufficiency in East Asia. Kadowaki T; Kadowaki S; Ohnishi H Front Immunol; 2021; 12():780689. PubMed ID: 34899744 [TBL] [Abstract][Full Text] [Related]
7. Mutation analysis of the TNFAIP3 in A20 haploinsufficiency: A case report. Yan M; Li D; Aknai S; Zhu H; Abudureyim M Medicine (Baltimore); 2021 May; 100(20):e25954. PubMed ID: 34011076 [TBL] [Abstract][Full Text] [Related]
8. [A report of clinical characteristics of 2 Chinese pedigrees with haploinsufficiency of A20 and literature review]. Zhong LQ; Wang W; Wang L; Jiang JJ; Shen M; Song HM Zhonghua Er Ke Za Zhi; 2019 Dec; 57(12):922-927. PubMed ID: 31795558 [No Abstract] [Full Text] [Related]
9. Case Report: A novel mutation in Cao C; Fu X; Wang X Front Endocrinol (Lausanne); 2023; 14():1131437. PubMed ID: 37324276 [TBL] [Abstract][Full Text] [Related]
10. An infant with A20 haploinsufficiency presenting with periodic fever syndrome: A case report. Wakatsuki R; Hatai Y; Okamoto K; Kaneko S; Shimbo A; Irabu H; Shimizu M; Kanegane H; Ono M Int J Rheum Dis; 2023 May; 26(5):973-976. PubMed ID: 36641803 [TBL] [Abstract][Full Text] [Related]
11. Haploinsufficiency of A20 (HA20): updates on the genetics, phenotype, pathogenesis and treatment. Yu MP; Xu XS; Zhou Q; Deuitch N; Lu MP World J Pediatr; 2020 Dec; 16(6):575-584. PubMed ID: 31587140 [TBL] [Abstract][Full Text] [Related]
12. A20 Haploinsufficiency in a Chinese Patient With Intestinal Behcet's Disease-Like Symptoms: A Case Report. Chen Y; Huang H; He Y; Chen M; Seidler U; Tian D; Xiao F Front Immunol; 2020; 11():1414. PubMed ID: 32719680 [No Abstract] [Full Text] [Related]
13. Three Chinese pedigrees of A20 haploinsufficiency: clinical, cytokine and molecular characterization. Tian Y; Wu B; Peng L; Wang J; Shen M Front Immunol; 2022; 13():955079. PubMed ID: 35958611 [TBL] [Abstract][Full Text] [Related]
14. DNGR1-mediated deletion of A20/Tnfaip3 in dendritic cells alters T and B-cell homeostasis and promotes autoimmune liver pathology. Das T; Bergen IM; Koudstaal T; van Hulst JAC; van Loo G; Boonstra A; Vanwolleghem T; Leung PSC; Gershwin ME; Hendriks RW; Kool M J Autoimmun; 2019 Aug; 102():167-178. PubMed ID: 31151831 [TBL] [Abstract][Full Text] [Related]
15. Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literature. Berteau F; Rouviere B; Delluc A; Nau A; Le Berre R; Sarrabay G; Touitou I; de Moreuil C Autoimmun Rev; 2018 Aug; 17(8):809-815. PubMed ID: 29890348 [TBL] [Abstract][Full Text] [Related]
16. Age Distribution of Multiple Functionally Relevant Subsets of CD4+ T Cells in Human Blood Using a Standardized and Validated 14-Color EuroFlow Immune Monitoring Tube. Botafogo V; Pérez-Andres M; Jara-Acevedo M; Bárcena P; Grigore G; Hernández-Delgado A; Damasceno D; Comans S; Blanco E; Romero A; Arriba-Méndez S; Gastaca-Abasolo I; Pedreira CE; van Gaans-van den Brink JAM; Corbiere V; Mascart F; van Els CACM; Barkoff AM; Mayado A; van Dongen JJM; Almeida J; Orfao A Front Immunol; 2020; 11():166. PubMed ID: 32174910 [TBL] [Abstract][Full Text] [Related]
17. Expanding the spectrum of A20 haploinsufficiency in two Chinese families: cases report. Li GM; Liu HM; Guan WZ; Xu H; Wu BB; Sun L BMC Med Genet; 2019 Jul; 20(1):124. PubMed ID: 31299923 [TBL] [Abstract][Full Text] [Related]
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19. A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease. Aeschlimann FA; Batu ED; Canna SW; Go E; Gül A; Hoffmann P; Leavis HL; Ozen S; Schwartz DM; Stone DL; van Royen-Kerkof A; Kastner DL; Aksentijevich I; Laxer RM Ann Rheum Dis; 2018 May; 77(5):728-735. PubMed ID: 29317407 [TBL] [Abstract][Full Text] [Related]
20. The Complexity of Being A20: From Biological Functions to Genetic Associations. Karri U; Harasimowicz M; Carpio Tumba M; Schwartz DM J Clin Immunol; 2024 Mar; 44(3):76. PubMed ID: 38451381 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]