Successful Renal Transplantation in MYH9-Related Disorder With Severe Macrothrombocytopenia: First Report in Korea
Author:
Publisher
Elsevier BV
Subject
Transplantation,Surgery
Reference15 articles.
1. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly;Kelley;Nat Genet,2000
2. Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome);Kunishima;Blood,2001
3. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium;Seri;Nat Genet,2000
4. Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes;Heath;Am J Hum Genet,2001
5. Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions;Kunishima;J Hum Genet,2001
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1. Successful renal transplantation following hemodialysis as bridging therapy in a patient with Fechtner syndrome: a case report and literature review;Renal Replacement Therapy;2023-10-04
2. Successful Kidney Transplantation in MYH-9-Related Disease Presenting with Severe Macrothrombocytopenia;Turkish Journal of Hematology;2023-09-01
3. Unusual Cause of Thrombocytopenia and Renal Failure in a 14-Year-Old Boy (MYH9-Associated Disorders);Case Reports in Nephrology and Dialysis;2023-05-15
4. Anaesthesia recommendations for MYH9-related disease (MYH9-RD);ANASTH INTENSIVMED;2023
5. Successful administration of eltrombopag in preparation for peritoneal dialysis catheter placement in a girl with MYH9-related disease;CEN Case Reports;2023-03-31
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