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1. A pediatric case of secondary T‐cell acute lymphoblastic leukemia with KMT2A‐MAML2 developing after hepatoblastoma treatment. Issue 1 (10th October 2019)

2. A Rapid Cytologic Double Staining of Epstein-Barr Virus–encoded Small RNA and Cell Surface Markers for Diagnosis of Epstein-Barr Virus–associated Hemophagocytic Lymphohistiocytosis. Issue 8 (November 2020)

3. Association of Multiple Gene Polymorphisms Including Homozygous NUDT15 R139C With Thiopurine Intolerance During the Treatment of Acute Lymphoblastic Leukemia. Issue 8 (November 2021)

4. Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21. Issue 4 (5th February 2020)

5. Diplotype analysis of NUDT15 variants and 6-mercaptopurine sensitivity in pediatric lymphoid neoplasms. Issue 12 (December 2018)

6. Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia. Issue 1 (10th January 2022)

7. Gene alterations involving the CRLF2‐JAK pathway and recurrent gene deletions in Down syndrome‐associated acute lymphoblastic leukemia in Japan. Issue 11 (16th July 2014)

8. Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing. Issue 3 (21st October 2019)

9. Isolated Bone Recurrence of Medulloblastoma With MYCN Amplification and TP53 Loss: A Case Report. Issue 2 (15th March 2022)

10. Isolated Bone Recurrence of Medulloblastoma With MYCN Amplification and TP53 Loss: A Case Report. Issue 2 (March 2022)