Ryuta Nishikomori

Professor

Kurume University School of Medicine

Japan

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About

Ryuta Nishikomori is a Professor at Kurume University School of Medicine in Japan. His research areas include the early diagnosis of genetic immunodeficiencies, pharmacokinetics, and the evaluation of unmet medical needs in rheumatic diseases. He has published recent articles on topics such as chronic granulomatous disease, autoimmune myocarditis, and novel genetic mutations linked to various syndromes.

Articles (12)

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2025

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2024

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2021

Collaborators (9)

Nan Yan

University of Texas Southwestern Medical Center

UNITED STATES

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Yutaro Yamada

Osaka University

JAPAN

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Hideki Fujii

Associate professor

Kobe University Graduate School of Medicine

JAPAN

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David F. Westneat

UNITED STATES

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Hiroyuki Wakiguchi

Yamaguchi University Graduate School of Medicine

JAPAN

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Kohsuke Imai

Professor and Chairman

National Defense Medical College

JAPAN

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Satoshi Okada

Professor

Hiroshima University

JAPAN

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Susumu Yamazaki

University of Tokyo Hospital

JAPAN

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Kazushi Izawa

JAPAN

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Ryuta Nishikomori

Research Interests

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Articles (12)

Early diagnosis of chronic granulomatous disease and McLeod syndrome via the use of a next generation sequencing

Pharmacokinetics, safety, and efficacy of 20% subcutaneous immunoglobulin (Ig20Gly) administered weekly or every 2 weeks in Japanese patients with primary immunodeficiency diseases: a phase 3, open-label study

Promoting awareness of terminology related to unmet medical needs in context of rheumatic diseases in Japan: a systematic review for evaluating unmet medical needs

Ultrasound and biopsy findings in arthritis with familial Mediterranean fever

Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease

Intracellular virus sensor MDA5 mutation develops autoimmune myocarditis and nephritis

A novel mutation in early-onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes.

Enzyme activity in dried blood spot as a diagnostic tool for adenosine deaminase 2 deficiency.

<i>NOD</i>2 Mutation-Associated Case with Blau Syndrome Triggered by BCG Vaccination

Case of cryopyrin‐associated periodic syndrome who recovered from growth delay by treatment with canakinumab

AIRE Gene Mutation Presenting at Age 2 Years With Autoimmune Retinopathy and Steroid-Responsive Acute Liver Failure: A Case Report and Literature Review

Aicardi-Goutières syndrome-like encephalitis in mutant mice with constitutively active MDA5

Collaborators (9)

Nan Yan

Yutaro Yamada

Hideki Fujii

David F. Westneat

Hiroyuki Wakiguchi

Kohsuke Imai

Satoshi Okada

Susumu Yamazaki

Kazushi Izawa

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