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Cited by in CrossRef
For: Schenone L, Notarantonio AB, Latger-Cannard V, Fremeaux-Bacchi V, De Carvalho-Bittencourt M, Rubio MT, Muller M, D'Aveni M. Allogeneic stem cell transplantation-A curative treatment for paroxysmal nocturnal hemoglobinuria with PIGT mutation: A case report. World J Clin Cases 2022; 10(17): 5702-5707 [PMID: 35979111 DOI: 10.12998/wjcc.v10.i17.5702]
URL: https://www.wjgnet.com/2307-8960/full/v10/i17/5702.htm
Number Citing Articles
1
Lucio Luzzatto, Shinji Nakao. Pathogenesis of paroxysmal nocturnal hemoglobinuriaBlood 2025; 145(26): 3077 doi: 10.1182/blood.2024025975
2
Yoshiko Murakami, Taroh Kinoshita. GPI Anchor and Its DeficiencyTrends in Glycoscience and Glycotechnology 2024; 36(209): J1 doi: 10.4052/tigg.2331.1J
3
Yoshiko Murakami, Taroh Kinoshita. GPI Anchor and Its DeficiencyTrends in Glycoscience and Glycotechnology 2024; 36(209): E1 doi: 10.4052/tigg.2331.1E
4
Qiangsheng Weng, Yajing Xu, Yan Chen, Can Liu, Ping Zhu, Mingyang Deng, Xin Li, Ling Nie, Zhongqing Wang, Bin Fu. Allogeneic Hematopoietic Cell Transplantation Using Post‐Transplant Cyclophosphamide in Patients With Large Paroxysmal Nocturnal Hemoglobinuria ClonesEuropean Journal of Haematology 2026;  doi: 10.1111/ejh.70162
5
Taroh Kinoshita. Towards a thorough understanding of mammalian glycosylphosphatidylinositol-anchored protein biosynthesisGlycobiology 2024; 34(11) doi: 10.1093/glycob/cwae061
6
Taroh Kinoshita. Clonal expansion mechanisms in paroxysmal nocturnal hemoglobinuriaInternational Journal of Hematology 2026;  doi: 10.1007/s12185-026-04167-5