Yusuke Tozawa

Absent X-linked inhibitor of apoptosis protein expression in T cell blasts and causal mutations including non-coding deletion.

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

Published: June 08, 2021

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

Journal: Modern rheumatology case reports

Published: October 22, 2020

A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).

Journal: Clinical immunology (Orlando, Fla.)

Published: May 17, 2019

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

Journal: Modern rheumatology

Published: March 14, 2018

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

Journal: Modern rheumatology

Published: March 14, 2018

Relapsing Polychondritis With Increased Bone Marrow Signal on Magnetic Resonance Imaging in a 13-Year-Old Girl.

Journal: Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

Published: September 28, 2017

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

Journal: Modern rheumatology

Published: June 15, 2017

Recurrence of juvenile dermatomyositis 8 years after remission.

Journal: JAAD case reports

Published: January 05, 2017

Preliminary study of optimal measurement location on vibroarthrography for classification of patients with knee osteoarthritis.

Journal: Journal of physical therapy science

Published: April 27, 2016

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

Journal: Clinical immunology (Orlando, Fla.)

Published: April 10, 2016

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

Journal: Modern rheumatology

Published: October 13, 2015

Radiological improvement by tocilizumab in polyarticular juvenile idiopathic arthritis.

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

Published: May 30, 2014

Absent X-linked inhibitor of apoptosis protein expression in T cell blasts and causal mutations including non-coding deletion.

Absent X-linked inhibitor of apoptosis protein expression in T cell blasts and causal mutations including non-coding deletion.

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

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

A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).

A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).

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

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

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

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

Relapsing Polychondritis With Increased Bone Marrow Signal on Magnetic Resonance Imaging in a 13-Year-Old Girl.

Relapsing Polychondritis With Increased Bone Marrow Signal on Magnetic Resonance Imaging in a 13-Year-Old Girl.

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

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

Recurrence of juvenile dermatomyositis 8 years after remission.

Recurrence of juvenile dermatomyositis 8 years after remission.

Preliminary study of optimal measurement location on vibroarthrography for classification of patients with knee osteoarthritis.

Preliminary study of optimal measurement location on vibroarthrography for classification of patients with knee osteoarthritis.

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

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

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

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

Radiological improvement by tocilizumab in polyarticular juvenile idiopathic arthritis.

Radiological improvement by tocilizumab in polyarticular juvenile idiopathic arthritis.

A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).

A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).