Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (7408)
All Articles published online
|
Publishing Process of This Article
|
May 26, 2020 (publication date) through Jul 24, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
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] |
|---|---|
| URL: | https://www.wjgnet.com/2307-8960/full/v8/i10/2001.htm |
| Number | Citing Articles |
| 1 |
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
|
| 2 |
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
|
| 3 |
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
|
| 4 |
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
|