| For: | Wang JF, Ma L, Gong XH, Cai C, Sun JJ. Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report. World J Clin Cases 2021; 9(19): 5245-5251 [PMID: 34307574 DOI: 10.12998/wjcc.v9.i19.5245] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i19/5245.htm |
| Number | Citing Articles |
| 1 |
Meiyun Kang, Huimin Li, Jun Zhu, Liwen Zhu, Yue Hong, Yongjun Fang. Clinical manifestations of 17 Chinese children with hereditary spherocytosis caused by novel mutations of the ANK1 gene and phenotypic analysis. Frontiers in Genetics 2023; 14 doi: 10.3389/fgene.2023.1088985
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| 2 |
Kritiya Rattanaseksan, Noppawan Tangbubpha, Praguywan Kadegasem, Tanyanee Khlangtan, Prathana Kongurai, Kanuengnit Emrat, Nongnuch Sirachainan, Pharuhad Pongmee, Duantida Songdej. Screening of hereditary elliptocytosis caused by SPTB mutations and identification of its association with significant jaundice among Thai neonates. BMJ Paediatrics Open 2026; 10(1) doi: 10.1136/bmjpo-2026-004778
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| 3 |
Yanfei Liu, Wanwei Li, Kun Zhou, Zhangxue Hu. Reverse complete heart block using transcutaneous pacing and repeated plasmapheresis in a neonate with lupus: a case report. Pediatric Rheumatology 2023; 21(1) doi: 10.1186/s12969-023-00920-w
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| 4 |
Bixin Xi, Siying Liu, Yongbing Zhu, Dedong Zhang, Yu Zhang, Aiguo Liu. Case report: Genetic analysis of a novel intronic inversion variant in the SPTB gene associated with hereditary spherocytosis. Frontiers in Genetics 2023; 14 doi: 10.3389/fgene.2023.1309040
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