Yukiko Oh

Tochigi, Japan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 17 publications

SLF2 and SMC5 dysfunction drives HSC aging and predisposes to MDS, defining a new inherited bone marrow failure syndrome.

SLF2 and SMC5 dysfunction drives HSC aging and predisposes to MDS, defining a new inherited bone marrow failure syndrome.

Journal: Leukemia

Published: February 05, 2026

High Plasma Presepsin Levels in Children With Hemophagocytic Lymphohistiocytosis.

High Plasma Presepsin Levels in Children With Hemophagocytic Lymphohistiocytosis.

Journal: Journal of pediatric hematology/oncology

Published: June 07, 2023

Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.

Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.

Journal: Nature communications

Published: November 11, 2021

Rapid blood cell recovery with immunosuppressive therapy combined with romiplostim in a patient with very severe hepatitis-associated aplastic anemia who underwent liver transplantation.

Rapid blood cell recovery with immunosuppressive therapy combined with romiplostim in a patient with very severe hepatitis-associated aplastic anemia who underwent liver transplantation.

Journal: International journal of hematology

Published: March 10, 2021

An immediate hypersensitivity reaction induced by PEGylated recombinant factor VIII.

An immediate hypersensitivity reaction induced by PEGylated recombinant factor VIII.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: March 26, 2020

Analysis of the BRAF and MAP2K1 mutations in patients with Langerhans cell histiocytosis in Japan.

Analysis of the BRAF and MAP2K1 mutations in patients with Langerhans cell histiocytosis in Japan.

Journal: International journal of hematology

Published: February 13, 2020

Cladribine-related myelodysplastic syndrome in Langerhans cell histiocytosis.

Cladribine-related myelodysplastic syndrome in Langerhans cell histiocytosis.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: July 30, 2018

Transient Marked Increase of γδ T Cells in WHIM Syndrome After Successful HSCT.

Transient Marked Increase of γδ T Cells in WHIM Syndrome After Successful HSCT.

Journal: Journal of clinical immunology

Published: February 23, 2018

Inflammatory serum cytokines and chemokines increase associated with the disease extent in pediatric Langerhans cell histiocytosis.

Inflammatory serum cytokines and chemokines increase associated with the disease extent in pediatric Langerhans cell histiocytosis.

Journal: Cytokine

Published: December 29, 2016

Successful allogeneic bone marrow transplantation with reduced intensity conditioning regimen for a pediatric relapsed ALK positive anaplastic large cell lymphoma.

Successful allogeneic bone marrow transplantation with reduced intensity conditioning regimen for a pediatric relapsed ALK positive anaplastic large cell lymphoma.

Journal: [Rinsho ketsueki] The Japanese journal of clinical hematology

Published: August 09, 2016

Molecular genetic and cytogenetic analysis of a primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma.

Molecular genetic and cytogenetic analysis of a primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma.

Journal: International journal of hematology

Published: April 16, 2015

Acute-phase ITIH4 levels distinguish multi-system from single-system Langerhans cell histiocytosis via plasma peptidomics.

Acute-phase ITIH4 levels distinguish multi-system from single-system Langerhans cell histiocytosis via plasma peptidomics.

Journal: Clinical proteomics

Published: March 26, 2015

Showing 1-12 of 17

Last Updated: 09/26/2026