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1. 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.

4. STING signalling is terminated through ESCRT-dependent microautophagy of vesicles originating from recycling endosomes

7. Aberrant RNA sensing in regulatory T cells causes systemic autoimmunity

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

10. Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency

15. Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency

17. Immunophenotyping of A20 haploinsufficiency by multicolor flow cytometry

18. Efficient detection of somatic UBA1 variants and clinical scoring system predicting patients with variants in VEXAS syndrome

20. BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies.

21. Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity

22. Corrigendum to “Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease”Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866.

25. Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency

26. Pyoderma gangrenosum, acne, and unclassified inflammatory bowel disease syndrome: A case report on a new subtype of pyogenic arthritis, pyoderma gangrenosum, and acne syndrome

27. Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations

32. Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases

33. Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1 :: CREM fusion presenting associated with IL ‐6/ STAT3 signaling

34. Additional file 1 of Efficacy and safety of baricitinib in Japanese patients with autoinflammatory type I interferonopathies (NNS/CANDLE, SAVI, And AGS)

36. Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1::CREM fusion presenting associated with IL‐6/STAT3 signaling.

37. Anti–Integrin αvβ6 Antibody as a Diagnostic Marker for Pediatric Patients With Ulcerative Colitis

38. Assessment of type I interferon signatures in undifferentiated inflammatory diseases: A Japanese multicenter experience

40. Gain-of-function mutations inALPK1cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome

41. Case Report: A Pediatric Case of Familial Mediterranean Fever Concurrent With Autoimmune Hepatitis

42. Fever of unknown origin caused by an intracranial mesenchymal tumor with a EWSR1-CREM fusion presenting associated with IL-6/STAT3 signaling

49. Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation

50. Novel AP3B1 mutations in a Hermansky–Pudlak syndrome type2 with neonatal interstitial lung disease

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