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Cited by in F6Publishing
For: Shabani M, Razaghian A, Alimadadi H, Shiari R, Shahrooei M, Parvaneh N. Different phenotypes of the same XIAP mutation in a family: A case of XIAP deficiency with juvenile idiopathic arthritis. Pediatr Blood Cancer 2019;66:e27593. [PMID: 30604482 DOI: 10.1002/pbc.27593] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Mudde ACA, Booth C, Marsh RA. Evolution of Our Understanding of XIAP Deficiency. Front Pediatr 2021;9:660520. [PMID: 34222142 DOI: 10.3389/fped.2021.660520] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Arnold DE, Nofal R, Wakefield C, Lehmberg K, Wustrau K, Albert MH, Morris EC, Heimall JR, Bunin NJ, Kumar A, Jordan MB, Cole T, Choo S, Brettig T, Speckmann C, Ehl S, Salamonowicz M, Wahlstrom J, Rao K, Booth C, Worth A, Marsh RA. Reduced-Intensity/Reduced-Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute GVHD. J Clin Immunol 2021. [PMID: 34586554 DOI: 10.1007/s10875-021-01103-6] [Reference Citation Analysis]
3 Speir M, Djajawi TM, Conos SA, Tye H, Lawlor KE. Targeting RIP Kinases in Chronic Inflammatory Disease. Biomolecules 2021;11:646. [PMID: 33924766 DOI: 10.3390/biom11050646] [Reference Citation Analysis]
4 Tang J, Zhou X, Wang L, Hu G, Zheng B, Wang C, Lu Y, Jin Y, Guo H, Liu Z. Eosinophilic colitis in a boy with a novel XIAP mutation: a case report. BMC Pediatr 2020;20:171. [PMID: 32305064 DOI: 10.1186/s12887-020-02075-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]