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May 26, 2020 (publication date) through Nov 23, 2024
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Publication Name
World Journal of Clinical Cases
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2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Kang LL, Liu ZL, Zhang HD. Gilbert’s syndrome coexisting with hereditary spherocytosis might not be rare: Six case reports. World J Clin Cases 2020; 8(10): 2001-2008 [PMID: 32518793 DOI: 10.12998/wjcc.v8.i10.2001] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v8/i10/2001.htm |
| Number | Citing Articles |
| 1 |
Yang Gou, Ping Wang, Wucheng Yang, Yimei Feng, Xiangui Peng, Hong Liu, Shuiqing Liu, Xi Zhang. A Case of Adult Hereditary Spherocytosis Concomitant with Gilbert Syndrome Caused by Mutations in SPTB and UGT1A1. Journal of Inflammation Research 2024; : 5977 doi: 10.2147/JIR.S483493
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| 2 |
Anika Agrawal, Jagdish Chandra. Gilbert syndrome in patients with inherited hemolytic anemia modifies the clinical phenotype. Pediatric Hematology Oncology Journal 2024; 9(2): 62 doi: 10.1016/j.phoj.2024.02.007
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| 3 |
Changwei Chi, Shenghao Wu, Wenjin Zhou, Yingying Hu, Yanwei Lu, Shanshan Weng. Coexistence of hereditary spherocytosis with SPTB P.Trp1150 gene variant and Gilbert syndrome: A case report and literature review. Open Life Sciences 2024; 19(1) doi: 10.1515/biol-2022-0904
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| 4 |
Dan Ji, Yu Peng, Yakun Zhang, Xinyi Tang, Mingyu Zhao, Longrong Ran, Xuelian Wu, Xin Luo, Shuang Chen, Tingting Jiang, Jun Li, Zailin Yang, Yao Liu. Recent advances and clinical applications of red blood cell lifespan measurement. Heliyon 2024; 10(17): e36507 doi: 10.1016/j.heliyon.2024.e36507
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| 5 |
Yafeng Wang, Linlin Liu, Dandan Liu, Wei Liu. A de novo ANK1 mutation in a childhood hereditary spherocytosis: a case report. BMC Pediatrics 2023; 23(1) doi: 10.1186/s12887-023-04092-0
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| 6 |
Liqing Yang, Huiying Shu, Min Zhou, Yuping Gong. Literature review on genotype–phenotype correlation in patients with hereditary spherocytosis. Clinical Genetics 2022; 102(6): 474 doi: 10.1111/cge.14223
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