These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 37388287)

  • 1. The spectrum of clinical presentation in haploinsufficiency of A20; a case report of a novel mutation in
    Debeljak M; Blazina S; Brecelj J; Avčin T; Toplak N
    Front Pediatr; 2023; 11():1132596. PubMed ID: 37388287
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two cases.
    Aslani N; Asnaashari K; Parvaneh N; Shahrooei M; Sotoudeh-Anvari M; Shahram F; Ziaee V
    Pediatr Rheumatol Online J; 2022 Sep; 20(1):78. PubMed ID: 36064566
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Genetic Mutations Associated With TNFAIP3 (A20) Haploinsufficiency and Their Impact on Inflammatory Diseases.
    Bagyinszky E; An SSA
    Int J Mol Sci; 2024 Jul; 25(15):. PubMed ID: 39125844
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. [A20 haploinsufficiency: what do clinicians need to know?].
    Elhani I; Aouba A; Riller Q; Vergneault H; Boursier G; Rieux-Laucat F; Hentgen V; Georgin-Lavialle S
    Rev Med Interne; 2024 Jul; 45(7):415-422. PubMed ID: 38160098
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The First Case of an Infant with Familial A20 Haploinsufficiency in Korea.
    Kim HY; Song JY; Kim WI; Ko HC; Park SE; Jang JH; Kim SH
    J Korean Med Sci; 2020 Aug; 35(30):e252. PubMed ID: 32743991
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Pseudodominance of autoinflammatory disease in a single Turkish family explained by co-inheritance of haploinsufficiency of A20 and familial Mediterranean fever.
    Horita N; Gül A; Aksentijevich I; Kastner D; Remmers EF
    Clin Exp Rheumatol; 2019; 37 Suppl 121(6):89-92. PubMed ID: 31376265
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. A novel missense mutation in TNFAIP3 causes haploinsufficiency of A20.
    Jiang W; Deng M; Gan C; Wang L; Mao H; Li Q
    Cell Immunol; 2022 Jan; 371():104453. PubMed ID: 34808442
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.