Shiho Nishimura
Hiroshima, Japan
Last Updated: 09/26/2026
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Found 15 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
Neonatal Stroke Following Placental Abruption in a Protein C-Deficient Mother-Infant Pair.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: October 05, 2025
Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.
Journal: The Journal of experimental medicine
Published: October 01, 2025
Age-specific incidence of joint disease in paediatric patients with haemophilia: A single-centre real-world outcome based on consecutive US examination.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: March 27, 2023
Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ.
Journal: The Journal of allergy and clinical immunology
Published: February 15, 2021
Pneumococcal Serotype-specific Opsonophagocytic Activity in Interleukin-1 Receptor-associated Kinase 4-deficient Patients.
Journal: The Pediatric infectious disease journal
Published: January 20, 2021
Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency.
Journal: Journal of immunology (Baltimore, Md. : 1950)
Published: December 30, 2020
IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation.
Journal: Journal of clinical immunology
Published: May 11, 2020
Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations.
Journal: International immunology
Published: May 09, 2020
Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusiondependent pyruvate kinase deficiency anemia.
Journal: Hematology reports
Published: September 13, 2019
Gain-of-Function STAT1 Mutation With Familial Lymphadenopathy and Hodgkin Lymphoma.
Journal: Frontiers in pediatrics
Published: December 01, 2018
Azacitidine successfully maintained the second remission in an infant with KMT2A-rearranged acute lymphoblastic leukemia who relapsed after unrelated cord blood transplantation.
Journal: Pediatric blood & cancer
Published: February 06, 2017
Last Updated: 09/26/2026