List of works - Masataka Ishimura

A Non-invasive Diagnosis of Histiocytic Necrotizing Lymphadenitis by Means of Gene Expression Profile Analysis of Peripheral Blood Mononuclear Cells ⬇️

scientific article published on April 23, 2013

A nationwide survey of common viral infections in childhood among patients with primary immunodeficiency diseases

scientific article published on 3 August 2016

Activated phosphoinositide 3-kinase δ syndrome presenting with gut-associated T-cell lymphoproliferative disease

scientific article published on January 2017

Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism

scientific article published on 15 September 2015

Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.

scientific article published on 23 February 2018

Cardiovascular complications associated with chronic active Epstein-Barr virus infection

scientific article published on 30 January 2009

Clonal origin of Epstein-Barr virus (EBV)-infected T/NK-cell subpopulations in EBV-positive T/NK-cell lymphoproliferative disorders of childhood ⬇️

scientific article published on March 5, 2011

Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome

scientific article published on 01 September 2018

Correction to: Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia

scientific article published on 01 August 2018

Correction: Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia

scientific article published on 14 October 2020

Diagnostic challenge of the newborn patients with heritable protein C deficiency

scientific article published on 23 October 2018

Disseminated Bacillus Calmette-Guérin lymphadenitis in a patient with gp91phox- chronic granulomatous disease 25 years after vaccination

scientific article published on 2 September 2008

Early progression of atherosclerosis in children with chronic infantile neurological cutaneous and articular syndrome

scientific article published on 11 May 2014

Early-onset sarcoidosis mimicking refractory cutaneous histiocytosis.

scientific article published on March 2008

Endocrine complications in primary immunodeficiency diseases in Japan.

scientific article published in October 2012

Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic Mutation

Epstein-Barr virus load in cerebrospinal fluid of patients with chronic active Epstein-Barr virus infection

scientific article published in November 2008

Erratum to: Long-term liposteroid therapy for idiopathic pulmonary hemosiderosis

scientific article published on 01 December 2015

Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency

scientific article published on 04 August 2015

Fever and Skin Involvement at Diagnosis Predicting the Intractable Langerhans Cell Histiocytosis: 40 Case-Series in a Single Center

scientific article published on 29 December 2017

Fulminant sepsis/meningitis due to Haemophilus influenzae in a protein C-deficient heterozygote treated with activated protein C therapy

scientific article published on 27 August 2008

Hemorrhagic Pneumonia as the First Manifestation of Anhidrotic Ectodermal Dysplasia with Immunodeficiency

scientific article published on 13 April 2019

Hepatitis-associated aplastic anemia during a primary infection of genotype 1a torque teno virus

scientific article published on 09 December 2009

Hypothyroidism and Levothyroxine-Responsive Liver Dysfunction in a Patient with Ring Chromosome 18 Syndrome ⬇️

scientific article published on September 4, 2012

Incomplete Kawasaki disease in a patient with chronic granulomatous disease

scientific article published on 01 June 2010

Limited renal prophylaxis in regular plasmatherapy for heritable ADAMTS13 deficiency ⬇️

scientific article published on April 29, 2013

Lipopolysaccharide-induced monocyte death in a novel ZnF7 domain mutation of TNFAIP3

scientific article published on 28 January 2020

Lipopolysaccharide-induced monocytic cell death for the diagnosis of mild neonatal-onset multisystem inflammatory disease

scientific article published on 01 June 2008

Long-term liposteroid therapy for idiopathic pulmonary hemosiderosis ⬇️

scientific article published on June 29, 2013

Malignant hepatic tumor occurring 10 yrs after a histocompatible sibling donor bone marrow transplantation for severe aplastic anemia

scientific article

Nephrolithiasis as an extra-intestinal presentation of pediatric inflammatory bowel disease unclassified ⬇️

scientific article published on June 30, 2010

Nontuberculous mycobacteria-associated hemophagocytic lymphohistiocytosis in MonoMAC syndrome

scientific article published on 01 March 2018

Posttransplant recipient-derived CD4 T-cell lymphoproliferative disease in X-linked hyper-IgM syndrome

scientific article published on 30 October 2018

Prognostic factors for survival of herpes simplex virus-associated hemophagocytic lymphohistiocytosis

scientific article published on 23 September 2019

Reappraising newborn screening for cobalamin C disorder.

scientific article published on 22 November 2017

Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia

scientific article published on 18 September 2020

Reduction in the Number of Varicella-Zoster Virus-Specific T-Cells in Immunocompromised Children with Varicella

scientific article published on 01 March 2020

Sjogren's syndrome-associated meningoencephalomyelitis: cerebrospinal fluid cytokine levels and therapeutic utility of tacrolimus

scientific article published on 9 November 2007

Streptococcus pyogenes-purpura fulminans as an invasive form of group A streptococcal infection.

scientific article published on 9 July 2018

Successful umbilical cord blood transplantation for severe chronic active Epstein-Barr virus infection after the double failure of hematopoietic stem cell transplantation

scientific article

Systemic Epstein-Barr Virus-Positive T/NK Lymphoproliferative Diseases With SH2D1A/XIAP Hypomorphic Gene Variants.

scientific article published on 21 May 2019

The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene

scientific article published on 23 January 2017

Thromboembolic complications in splenectomized patients with dominantly inherited beta-thalassemia

scientific article published on 27 August 2008

Thrombotic microangiopathy in a very young infant with mitral valvuloplasty

scientific article published on 7 February 2018

Transient Hemi-Lower Limb Ischemia in the Newborn: Arterial Thrombosis or Persistent Sciatic Artery?

scientific article published on January 2017

Treatment choice of immunotherapy or further chemotherapy for Epstein–Barr virus‐associated hemophagocytic lymphohistiocytosis ⬇️

scientific article published on December 19, 2011

Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6.

scientific article

List of works by Masataka Ishimura

A Non-invasive Diagnosis of Histiocytic Necrotizing Lymphadenitis by Means of Gene Expression Profile Analysis of Peripheral Blood Mononuclear Cells ⬇️

A nationwide survey of common viral infections in childhood among patients with primary immunodeficiency diseases

Activated phosphoinositide 3-kinase δ syndrome presenting with gut-associated T-cell lymphoproliferative disease

Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism

Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.

Cardiovascular complications associated with chronic active Epstein-Barr virus infection

Clonal origin of Epstein-Barr virus (EBV)-infected T/NK-cell subpopulations in EBV-positive T/NK-cell lymphoproliferative disorders of childhood ⬇️

Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome

Correction to: Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia

Correction: Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia

Diagnostic challenge of the newborn patients with heritable protein C deficiency

Disseminated Bacillus Calmette-Guérin lymphadenitis in a patient with gp91phox- chronic granulomatous disease 25 years after vaccination

Early progression of atherosclerosis in children with chronic infantile neurological cutaneous and articular syndrome

Early-onset sarcoidosis mimicking refractory cutaneous histiocytosis.

Endocrine complications in primary immunodeficiency diseases in Japan.

Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic Mutation

Epstein-Barr virus load in cerebrospinal fluid of patients with chronic active Epstein-Barr virus infection

Erratum to: Long-term liposteroid therapy for idiopathic pulmonary hemosiderosis

Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency

Fever and Skin Involvement at Diagnosis Predicting the Intractable Langerhans Cell Histiocytosis: 40 Case-Series in a Single Center

Fulminant sepsis/meningitis due to Haemophilus influenzae in a protein C-deficient heterozygote treated with activated protein C therapy

Hemorrhagic Pneumonia as the First Manifestation of Anhidrotic Ectodermal Dysplasia with Immunodeficiency

Hepatitis-associated aplastic anemia during a primary infection of genotype 1a torque teno virus

Hypothyroidism and Levothyroxine-Responsive Liver Dysfunction in a Patient with Ring Chromosome 18 Syndrome ⬇️

Incomplete Kawasaki disease in a patient with chronic granulomatous disease

Limited renal prophylaxis in regular plasmatherapy for heritable ADAMTS13 deficiency ⬇️

Lipopolysaccharide-induced monocyte death in a novel ZnF7 domain mutation of TNFAIP3

Lipopolysaccharide-induced monocytic cell death for the diagnosis of mild neonatal-onset multisystem inflammatory disease

Long-term liposteroid therapy for idiopathic pulmonary hemosiderosis ⬇️

Malignant hepatic tumor occurring 10 yrs after a histocompatible sibling donor bone marrow transplantation for severe aplastic anemia

Nephrolithiasis as an extra-intestinal presentation of pediatric inflammatory bowel disease unclassified ⬇️

Nontuberculous mycobacteria-associated hemophagocytic lymphohistiocytosis in MonoMAC syndrome

Posttransplant recipient-derived CD4 T-cell lymphoproliferative disease in X-linked hyper-IgM syndrome

Prognostic factors for survival of herpes simplex virus-associated hemophagocytic lymphohistiocytosis

Reappraising newborn screening for cobalamin C disorder.

Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia

Reduction in the Number of Varicella-Zoster Virus-Specific T-Cells in Immunocompromised Children with Varicella

Sjogren's syndrome-associated meningoencephalomyelitis: cerebrospinal fluid cytokine levels and therapeutic utility of tacrolimus

Streptococcus pyogenes-purpura fulminans as an invasive form of group A streptococcal infection.

Successful umbilical cord blood transplantation for severe chronic active Epstein-Barr virus infection after the double failure of hematopoietic stem cell transplantation

Systemic Epstein-Barr Virus-Positive T/NK Lymphoproliferative Diseases With SH2D1A/XIAP Hypomorphic Gene Variants.

The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene

Thromboembolic complications in splenectomized patients with dominantly inherited beta-thalassemia

Thrombotic microangiopathy in a very young infant with mitral valvuloplasty

Transient Hemi-Lower Limb Ischemia in the Newborn: Arterial Thrombosis or Persistent Sciatic Artery?

Treatment choice of immunotherapy or further chemotherapy for Epstein–Barr virus‐associated hemophagocytic lymphohistiocytosis ⬇️

Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6.