List of works - Ichiro Kobayashi

A 75-kD autoantigen recognized by sera from patients with X-linked autoimmune enteropathy associated with nephropathy

scientific article published on 01 March 1998

A Post-Liver Transplant Girl With Recurrent Cramps in the Legs.

scientific article published on 8 January 2015

A heterozygous dominant-negative mutation in the coiled-coil domain of STAT1 is the cause of autosomal-dominant Mendelian susceptibility to mycobacterial diseases.

scientific article

Anti-melanoma differentiation-associated gene 5 antibody is a diagnostic and predictive marker for interstitial lung diseases associated with juvenile dermatomyositis

scientific article published on 13 January 2011

Autoantibodies to villin occur frequently in IPEX, a severe immune dysregulation, syndrome caused by mutation of FOXP3.

scientific article

Autoimmune haemolytic anaemia caused by anti-M antibody in a patient with Kawasaki disease

scientific article published on 05 November 2019

Chronic mucocutaneous candidiasis caused by a gain-of-function mutation in the STAT1 DNA-binding domain.

scientific article

Clinical practice guidance for juvenile dermatomyositis (JDM) 2018-Update

scientific article published on 03 February 2020

Coexistence of acute poststreptococcal glomerulonephritis and acute rheumatic fever in a Japanese girl with primary Sjögren's syndrome

scientific article published on 18 February 2020

Complications of childhood Sjögren syndrome

scientific article published on 01 October 1996

Determination of the deletion breakpoints in two patients with contiguous gene syndrome encompassing CYBB gene.

scientific article published on 21 September 2010

Development of germinoma during the treatment of systemic-onset juvenile idiopathic arthritis with infliximab

scientific article published on 10 November 2011

Difference in target antigens between central tolerance and peripheral tolerance deficiencies

scientific article (publication date: 2015)

Difficulty in the diagnosis of bone and joint pain associated with pediatric acute leukemia; comparison with juvenile idiopathic arthritis

scientific article published on 14 June 2017

Disease specificity of anti-tryptophan hydroxylase-1 and anti-AIE-75 autoantibodies in APECED and IPEX syndrome

scientific article published on 08 November 2014

Elevation of serum IgE level and peripheral eosinophil count during T lymphocyte-directed gene therapy for ADA deficiency: implication of Tc2-like cells after gene transduction procedure.

scientific article published in November 1998

Evaluation of systemic activity of pediatric primary Sjögren's syndrome by EULAR Sjögren's syndrome disease activity index (ESSDAI)

scientific article published on 09 April 2018

Expression of AIE-75 PDZ-domain protein induces G2/M cell cycle arrest in human colorectal adenocarcinoma SW480 cells

scientific article

Extremely high serum level of IgE during immunosuppressive therapy: paradoxical effect of cyclosporine A and tacrolimus

scientific article published on 01 April 1997

Fusarium falciforme infection in a patient with chronic granulomatous disease: Unique long-term course of epidural abscess

scientific article published on 01 January 2015

Interaction of MCC2, a novel homologue of MCC tumor suppressor, with PDZ-domain Protein AIE-75

scientific article

Monocyte/macrophage-specific NADPH oxidase contributes to antimicrobial host defense in X-CGD.

scientific article

Myositis-specific autoantibodies in Japanese patients with juvenile idiopathic inflammatory myopathies

scientific article published on 09 April 2018

Pediatric Rheumatology Association of Japan recommendation for vaccination in pediatric rheumatic diseases

scientific article

Progression of palindromic rheumatism to juvenile idiopathic arthritis in a Japanese girl carrying heterozygous L110P-E148Q substitutions of MEFV gene.

scientific article published on 12 October 2015

Rapid progression to pulmonary arterial hypertension crisis associated with mixed connective tissue disease in an 11-year-old girl.

scientific article published on 18 May 2013

Rapidly progressive and fatal neurocutaneous melanosis presenting as recurrent headache

scientific article published on 01 April 2013

Recurrence of juvenile dermatomyositis 8 years after remission

scientific article published on 26 December 2016

Somatic mosaicism in two unrelated patients with X-linked chronic granulomatous disease characterized by the presence of a small population of normal cells ⬇️

scientific article published on January 28, 2012

Stroke During Norovirus Infection as the Initial Episode of Antiphospholipid Syndrome.

scientific article published on 8 February 2016

Successful peripheral T-lymphocyte-directed gene transfer for a patient with severe combined immune deficiency caused by adenosine deaminase deficiency ⬇️

scientific article published on January 1, 1998

Tacrolimus in combination with methotrexate and corticosteroid for the treatment of child-onset anti-signal recognition particle antibody-positive necrotizing myopathy.

scientific article published on 29 November 2016

Two novel gain-of-function mutations of STAT1 responsible for chronic mucocutaneous candidiasis disease: impaired production of IL-17A and IL-22, and the presence of anti-IL-17F autoantibody.

scientific article published on 6 October 2014

List of works by Ichiro Kobayashi

A 75-kD autoantigen recognized by sera from patients with X-linked autoimmune enteropathy associated with nephropathy

A Post-Liver Transplant Girl With Recurrent Cramps in the Legs.

A heterozygous dominant-negative mutation in the coiled-coil domain of STAT1 is the cause of autosomal-dominant Mendelian susceptibility to mycobacterial diseases.

Anti-melanoma differentiation-associated gene 5 antibody is a diagnostic and predictive marker for interstitial lung diseases associated with juvenile dermatomyositis

Autoantibodies to villin occur frequently in IPEX, a severe immune dysregulation, syndrome caused by mutation of FOXP3.

Autoimmune haemolytic anaemia caused by anti-M antibody in a patient with Kawasaki disease

Chronic mucocutaneous candidiasis caused by a gain-of-function mutation in the STAT1 DNA-binding domain.

Clinical practice guidance for juvenile dermatomyositis (JDM) 2018-Update

Coexistence of acute poststreptococcal glomerulonephritis and acute rheumatic fever in a Japanese girl with primary Sjögren's syndrome

Complications of childhood Sjögren syndrome

Determination of the deletion breakpoints in two patients with contiguous gene syndrome encompassing CYBB gene.

Development of germinoma during the treatment of systemic-onset juvenile idiopathic arthritis with infliximab

Difference in target antigens between central tolerance and peripheral tolerance deficiencies

Difficulty in the diagnosis of bone and joint pain associated with pediatric acute leukemia; comparison with juvenile idiopathic arthritis

Disease specificity of anti-tryptophan hydroxylase-1 and anti-AIE-75 autoantibodies in APECED and IPEX syndrome

Elevation of serum IgE level and peripheral eosinophil count during T lymphocyte-directed gene therapy for ADA deficiency: implication of Tc2-like cells after gene transduction procedure.

Evaluation of systemic activity of pediatric primary Sjögren's syndrome by EULAR Sjögren's syndrome disease activity index (ESSDAI)

Expression of AIE-75 PDZ-domain protein induces G2/M cell cycle arrest in human colorectal adenocarcinoma SW480 cells

Extremely high serum level of IgE during immunosuppressive therapy: paradoxical effect of cyclosporine A and tacrolimus

Fusarium falciforme infection in a patient with chronic granulomatous disease: Unique long-term course of epidural abscess

Interaction of MCC2, a novel homologue of MCC tumor suppressor, with PDZ-domain Protein AIE-75

Monocyte/macrophage-specific NADPH oxidase contributes to antimicrobial host defense in X-CGD.

Myositis-specific autoantibodies in Japanese patients with juvenile idiopathic inflammatory myopathies

Pediatric Rheumatology Association of Japan recommendation for vaccination in pediatric rheumatic diseases

Progression of palindromic rheumatism to juvenile idiopathic arthritis in a Japanese girl carrying heterozygous L110P-E148Q substitutions of MEFV gene.

Rapid progression to pulmonary arterial hypertension crisis associated with mixed connective tissue disease in an 11-year-old girl.

Rapidly progressive and fatal neurocutaneous melanosis presenting as recurrent headache

Recurrence of juvenile dermatomyositis 8 years after remission

Somatic mosaicism in two unrelated patients with X-linked chronic granulomatous disease characterized by the presence of a small population of normal cells ⬇️

Stroke During Norovirus Infection as the Initial Episode of Antiphospholipid Syndrome.

Successful peripheral T-lymphocyte-directed gene transfer for a patient with severe combined immune deficiency caused by adenosine deaminase deficiency ⬇️

Tacrolimus in combination with methotrexate and corticosteroid for the treatment of child-onset anti-signal recognition particle antibody-positive necrotizing myopathy.

Two novel gain-of-function mutations of STAT1 responsible for chronic mucocutaneous candidiasis disease: impaired production of IL-17A and IL-22, and the presence of anti-IL-17F autoantibody.