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Cited by in CrossRef
For: Jiang N, Mao WY, Peng BX, Yang TY, Mao XR. Clinical manifestations of adult hereditary spherocytosis with novel SPTB gene mutations and hyperjaundice: A case report. World J Clin Cases 2023; 11(6): 1349-1355 [PMID: 36926142 DOI: 10.12998/wjcc.v11.i6.1349]
URL: https://www.wjgnet.com/2307-8960/full/v11/i6/1349.htm
Number Citing Articles
1
Xiaobing Li, Tingqiang Zhang, Xuemei Li, Li Wang, Qian Li, Qianqian Liu, Chengyin He, Li Zhang, Yongsheng Liu, Junling Tang. Identification of a novel SPTB gene splicing mutation in hereditary spherocytosis: a case report and diagnostic insightsFrontiers in Genetics 2025; 15 doi: 10.3389/fgene.2024.1522204
2
Sintayehu Mekonnen, Dereje Adefris, Belete Shikuro, Abdi Bati, Daniel Azmeraw, Temesegen Kassa, Eliud Teshome, Hawi Farris. Complications of delayed diagnosis and challenges: successfully managed SPTB gene variant hereditary spherocytosis with hepatocellular jaundice—a case reportJournal of Medical Case Reports 2024; 18(1) doi: 10.1186/s13256-024-04872-x
3
Sana Habibzadeh, Majid Einakchi, Mohammad Ebrahim Kalantari, Farnood Forouhar, Arefeh Ma'souminejad. The coincidence of beta‐thalassemia and hereditary spherocytosis: A case report and literature reviewClinical Case Reports 2024; 12(6) doi: 10.1002/ccr3.9080