206 related articles for article (PubMed ID: 32719680)
21. Clinical characteristics and genetic analysis of A20 haploinsufficiency.
Zhang D; Su G; Zhou Z; Lai J
Pediatr Rheumatol Online J; 2021 May; 19(1):75. PubMed ID: 34030699
[TBL] [Abstract][Full Text] [Related]
22. Coinheritance of generalized pustular psoriasis and familial Behçet-like autoinflammatory syndrome with variants in IL36RN and TNFAIP3 in the heterozygous state.
Liang J; Zhang H; Guo Y; Yang K; Ni C; Yu H; Kong X; Li M; Lu Z; Yao Z
J Dermatol; 2019 Oct; 46(10):907-910. PubMed ID: 31353537
[TBL] [Abstract][Full Text] [Related]
23. [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]
24. Case Report: An early-onset inflammatory colitis due to a variant in
Zanatta L; Biscaro F; Bresolin S; Marzaro M; Sarcognato S; Cataldo I; Marzollo A; Martelossi S
Front Pediatr; 2022; 10():1044007. PubMed ID: 36467491
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Haploinsufficiency of A20 and other paediatric inflammatory disorders with mucosal involvement.
Aeschlimann FA; Laxer RM
Curr Opin Rheumatol; 2018 Sep; 30(5):506-513. PubMed ID: 29916847
[TBL] [Abstract][Full Text] [Related]
27. Autosomal dominant Hashimoto's thyroiditis with a mutation in
Hori T; Ohnishi H; Kadowaki T; Kawamoto N; Matsumoto H; Ohara O; Fukao T
Clin Pediatr Endocrinol; 2019; 28(3):91-96. PubMed ID: 31384100
[TBL] [Abstract][Full Text] [Related]
28. [A woman in her thirties with frequent mucosal ulcers].
Bitter H; Midtvedt Ø; Gunnarsson R; Lande A
Tidsskr Nor Laegeforen; 2023 May; 143(8):. PubMed ID: 37254975
[TBL] [Abstract][Full Text] [Related]
29. Novel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's disease.
Shigemura T; Kaneko N; Kobayashi N; Kobayashi K; Takeuchi Y; Nakano N; Masumoto J; Agematsu K
RMD Open; 2016; 2(1):e000223. PubMed ID: 27175295
[TBL] [Abstract][Full Text] [Related]
30. Haploinsufficiency of A20 with a novel mutation of deletion of exons 2-3 of
Shimizu M; Matsubayashi T; Ohnishi H; Nakama M; Izawa K; Honda Y; Nishikomori R
Mod Rheumatol; 2021 Mar; 31(2):493-497. PubMed ID: 32011208
[TBL] [Abstract][Full Text] [Related]
31. Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome.
Takagi M; Ogata S; Ueno H; Yoshida K; Yeh T; Hoshino A; Piao J; Yamashita M; Nanya M; Okano T; Kajiwara M; Kanegane H; Muramatsu H; Okuno Y; Shiraishi Y; Chiba K; Tanaka H; Bando Y; Kato M; Hayashi Y; Miyano S; Imai K; Ogawa S; Kojima S; Morio T
J Allergy Clin Immunol; 2017 Jun; 139(6):1914-1922. PubMed ID: 27845235
[TBL] [Abstract][Full Text] [Related]
32. Haploinsufficiency of A20 caused by a novel pathogenic missense variant of TNFAIP3 and successfully treated with anti-TNF and immunosuppressive therapies.
Lina S; Ya'nan H; Ying Y; Fengfan W; Xin H; Xiaoxia R; Ying F
Cell Immunol; 2023; 391-392():104753. PubMed ID: 37535999
[TBL] [Abstract][Full Text] [Related]
33. TNFAIP3 haploinsufficiency is the cause of autoinflammatory manifestations in a patient with a deletion of 13Mb on chromosome 6.
Franco-Jarava C; Wang H; Martin-Nalda A; Alvarez SD; García-Prat M; Bodet D; García-Patos V; Plaja A; Rudilla F; Rodriguez-Sureda V; García-Latorre L; Aksentijevich I; Colobran R; Soler-Palacín P
Clin Immunol; 2018 Jun; 191():44-51. PubMed ID: 29572183
[TBL] [Abstract][Full Text] [Related]
34. Functional analysis of novel A20 variants in patients with atypical inflammatory diseases.
Kadowaki S; Hashimoto K; Nishimura T; Kashimada K; Kadowaki T; Kawamoto N; Imai K; Okada S; Kanegane H; Ohnishi H
Arthritis Res Ther; 2021 Feb; 23(1):52. PubMed ID: 33549127
[TBL] [Abstract][Full Text] [Related]
35. Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease.
Zhou Q; Wang H; Schwartz DM; Stoffels M; Park YH; Zhang Y; Yang D; Demirkaya E; Takeuchi M; Tsai WL; Lyons JJ; Yu X; Ouyang C; Chen C; Chin DT; Zaal K; Chandrasekharappa SC; Hanson EP; Yu Z; Mullikin JC; Hasni SA; Wertz IE; Ombrello AK; Stone DL; Hoffmann P; Jones A; Barham BK; Leavis HL; van Royen-Kerkof A; Sibley C; Batu ED; Gül A; Siegel RM; Boehm M; Milner JD; Ozen S; Gadina M; Chae J; Laxer RM; Kastner DL; Aksentijevich I
Nat Genet; 2016 Jan; 48(1):67-73. PubMed ID: 26642243
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Decreased expression of A20 is associated with ocular Behcet's disease (BD) but not with Vogt-Koyanagi-Harada (VKH) disease.
He Y; Wang C; Su G; Deng B; Ye Z; Huang Y; Yuan G; Aize K; Li H; Yang P
Br J Ophthalmol; 2018 Aug; 102(8):1167-1172. PubMed ID: 29699987
[TBL] [Abstract][Full Text] [Related]
38. A20 haploinsufficiency in a neonate caused by a large deletion on chromosome 6q.
Zhang F; Zhang L
Pediatr Rheumatol Online J; 2024 Jan; 22(1):12. PubMed ID: 38183052
[TBL] [Abstract][Full Text] [Related]
39. [Not Available].
Elhani I; Aouba A; Riller Q; Vergneault H; Boursier G; Rieux-Laucat F; Hentgen V; Georgin-Lavialle S
Rev Med Interne; 2023 Dec; ():. PubMed ID: 38160098
[TBL] [Abstract][Full Text] [Related]
40. Infantile Onset Intractable Inflammatory Bowel Disease Due to Novel Heterozygous Mutations in TNFAIP3 (A20).
Zheng C; Huang Y; Ye Z; Wang Y; Tang Z; Lu J; Wu J; Zhou Y; Wang L; Huang Z; Yang H; Xue A
Inflamm Bowel Dis; 2018 Nov; 24(12):2613-2620. PubMed ID: 29788367
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]