Journal Report

Intractable and Rare Diseases Research

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Journal Information
Journal Title
Intractable and Rare Diseases Research
Publisher
International Advancement Center for Medicine and Health Research Co., Ltd.
ISSN
2186-3644
E-ISSN
2186-361X
Database
SCOPUS
Domain
Health Sciences, Life Sciences, Social Sciences
Classification History
Year A+ A B C
2026 ✓
2025 ✓
2024 ✓
2023 ✓
2021/2022 ✓
2020 ✓
2019 ✓
2018
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Mitochondrial DNA A3243G variant-associated MELAS: Recent advances in clinical trials, therapeutic interventions, and disease-modifying strategies
Kuan-Yu Chu
2026-8-31 Vol. 15 Issue 3 Pages 219-231
DOI: 10.5582/irdr.2026.01026
Skeletal involvement in Joubert syndrome: From low bone mineral density to severe secondary osteoporosis
Tatsiana Babina, Bogumiła Alicja Górczewska, Elżbieta Jakubowska-Pietkiewicz
2026-8-31 Vol. 15 Issue 3 Pages 277-279
DOI: 10.5582/irdr.2026.01020
Traditional Chinese medicine research on rare diseases: Publication trends and future perspectives
Li-ming Chen, Xin-yi Chen, Bo-wen Liu et al.
2026-8-31 Vol. 15 Issue 3 Pages 268-272
DOI: 10.5582/irdr.2026.01041
Fulminant myocarditis and sudden death associated with thymoma-related autoimmunity
Ying Liu, Xue Yin, Baitong Wang et al.
2026-8-31 Vol. 15 Issue 3 Pages 273-276
DOI: 10.5582/irdr.2026.01022
Japanese intractable and rare dermatologic diseases: From the official skin-centered nanbyo core to an illustrative mechanism-based framework
Yue Han, Tian-Ge Qin, Peipei Song
2026-8-31 Vol. 15 Issue 3 Pages 200-218
DOI: 10.5582/irdr.2026.01061
Cutaneous lymphomas reported following the use of dupilumab, nemolizumab, tralokinumab, or lebrikizumab: A case investigation based on JADER database and disproportionality analysis
Hiroyuki Tanaka, Toshihiro Ishii
2026-8-31 Vol. 15 Issue 3 Pages 247-253
DOI: 10.5582/irdr.2026.01017
Prenatal molecularly supported diagnosis of a fetus with urinary malformation caused by novel compound heterozygous variants in the <i>FAM149B1</i> gene
Jinyu Liu, Yi Wu, Shixuan Xu et al.
2026-8-31 Vol. 15 Issue 3 Pages 260-267
DOI: 10.5582/irdr.2026.01029
Generation and characterization of induced pluripotent stem cells from a patient with classic Fabry disease
Guowei Li, Jing Luan, Zihan Li et al.
2026-8-31 Vol. 15 Issue 3 Pages 254-259
DOI: 10.5582/irdr.2026.01023
Phenotypic variability of Fragile-X syndrome in Asian population: A systematic review
Christina L Minar Napitupulu, Jeslyn Tengkawan, Agustini Utari et al.
2026-8-31 Vol. 15 Issue 3 Pages 232-246
DOI: 10.5582/irdr.2026.01037
A neurologist's guide to VEXAS syndrome: Differentiating somatic autoinflammation from autoimmune mimics
Nikolaos Mitsoudis, Ioannis Nikolakakis, Athanasia Apsemidou et al.
2026-5-31 Vol. 15 Issue 2 Pages 166-172
DOI: 10.5582/irdr.2026.01013
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Printed: November 4, 2026 09:51