Yuhachi Ikeda

Otsu, Japan

Last Updated: 09/26/2026

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Found 13 publications

Severe hypophosphataemia following denosumab administration successfully managed using a calcimimetic agent.

Severe hypophosphataemia following denosumab administration successfully managed using a calcimimetic agent.

Journal: BMJ case reports

Published: January 08, 2025

Incidence of Bloodstream Infections in Pediatric Patients with Cancer during Febrile Neutropenia: A Retrospective Study.

Incidence of Bloodstream Infections in Pediatric Patients with Cancer during Febrile Neutropenia: A Retrospective Study.

Journal: JMA journal

Published: November 18, 2024

Persistent candidemia and Candida endophthalmitis with relapsed acute lymphoblastic leukemia.

Persistent candidemia and Candida endophthalmitis with relapsed acute lymphoblastic leukemia.

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

Published: May 20, 2024

Effect of Early Physical Therapy on Children of School Age With Hematological Cancer: A Quasi-Randomized Controlled Pilot Study.

Effect of Early Physical Therapy on Children of School Age With Hematological Cancer: A Quasi-Randomized Controlled Pilot Study.

Journal: Pediatric physical therapy : the official publication of the Section on Pediatrics of the American Physical Therapy Association

Published: October 10, 2023

Allogeneic Hematopoietic Cell Transplantation Ameliorated Asymptomatic Granulomatous and Lymphocytic Interstitial Lung Disease in a Patient With XIAP Deficiency.

Allogeneic Hematopoietic Cell Transplantation Ameliorated Asymptomatic Granulomatous and Lymphocytic Interstitial Lung Disease in a Patient With XIAP Deficiency.

Journal: Journal of pediatric hematology/oncology

Published: July 10, 2023

Familial hemophagocytic lymphohistiocytosis syndrome due to lysinuric protein intolerance: a patient with a novel compound heterozygous pathogenic variant in SLC7A7.

Familial hemophagocytic lymphohistiocytosis syndrome due to lysinuric protein intolerance: a patient with a novel compound heterozygous pathogenic variant in SLC7A7.

Journal: International journal of hematology

Published: March 08, 2022

Chronic-phase chronic myeloid leukemia with intracranial hemorrhage complicated with tumor lysis syndrome

Chronic-phase chronic myeloid leukemia with intracranial hemorrhage complicated with tumor lysis syndrome

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

Published: June 10, 2021

Successful management of acute chest syndrome in a patient with sickle cell disease

Successful management of acute chest syndrome in a patient with sickle cell disease

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

Published: June 07, 2019

Characteristics of methotrexate-induced stroke-like neurotoxicity.

Characteristics of methotrexate-induced stroke-like neurotoxicity.

Journal: International journal of hematology

Published: July 05, 2018

Addition of High-Dose Cytarabine to Fludarabine-Based Conditioning for Hematopoietic Stem Cell Transplantation for Treating Fanconi Anemia Patients with Advanced Myeloid Malignancy: A Single-Center Experience and Literature Review.

Addition of High-Dose Cytarabine to Fludarabine-Based Conditioning for Hematopoietic Stem Cell Transplantation for Treating Fanconi Anemia Patients with Advanced Myeloid Malignancy: A Single-Center Experience and Literature Review.

Journal: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

Published: April 03, 2016

A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele.

A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele.

Journal: Journal of clinical immunology

Published: September 08, 2014

Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome.

Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome.

Journal: Molecular immunology

Published: November 05, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026