Keishiro Kinoshita
Fukuoka, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.
Journal: medRxiv : the preprint server for health sciences
Published: August 01, 2026
Anti-SMN complex antibodies in paediatric mixed connective tissue disease with interstitial lung disease: clinical and immunological insights.
Journal: Rheumatology advances in practice
Published: June 18, 2026
Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.
Journal: The Journal of experimental medicine
Published: October 01, 2025
Long-term outcomes of chronic active Epstein-Barr virus infection in childhood after dominantly infected lymphocyte subpopulation management.
Journal: The Journal of infectious diseases
Published: July 25, 2025
Early-Onset Antibody-Dependent Pure Red Cell Aplasia Associated With STAT3 Gain-of-Function.
Journal: Pediatric blood & cancer
Published: February 25, 2025
Monocyte STAT1 phosphorylation and treatment response of JAK inhibitors in chronic nonbacterial osteomyelitis.
Journal: Pediatric rheumatology online journal
Published: September 06, 2024
Epstein-Barr virus monitoring for preemptive re-hematopoietic cell transplantation in CD3δ-deficient siblings.
Journal: Pediatric blood & cancer
Published: May 06, 2024
Pretransplant ribavirin and interferon-α therapy for rhinovirus interstitial pneumonia in a RAG1-deficient infant.
Journal: Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy
Published: June 14, 2023
De novo p.G696S mutation in COL4A1 causes intracranial calcification and late-onset cerebral hemorrhage: A case report and review of the literature.
Journal: European journal of medical genetics
Published: June 05, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026