MYH9-related disease with a normal platelet count
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s13730-024-00922-x.pdf
Reference14 articles.
1. Singh N, Nainani N, Arora P, et al. CKD in MYH9-related disorders. Am J Kidney Dis. 2009;54(4):732–40. https://doi.org/10.1053/j.ajkd.2009.06.023.
2. Tabibzadeh N, Fleury D, Labatut D, et al. MYH9-related disorders display heterogeneous kidney involvement and outcome. Clin Kidney J. 2019;12(4):494–502. https://doi.org/10.1093/ckj/sfy117.
3. Uemura O, Nagai T, Ishikura K, et al. Creatinine-based equation to estimate the glomerular filtration rate in Japanese children and adolescents with chronic kidney disease. Clin Exp Nephrol. 2014;18(4):626–33. https://doi.org/10.1007/s10157-013-0856-y.
4. Kunishima S, Kojima T, Matsushita T, et al. Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome). Blood. 2001;97(4):1147–9. https://doi.org/10.1182/blood.v97.4.1147.
5. Shirai Y, Miura K, Hamada R, et al. A nationwide survey of MYH9-related disease in Japan. Clin Exp Nephrol. 2024;28(1):40–9. https://doi.org/10.1007/s10157-023-02404-3.
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