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

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

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

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

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

16. List of Contributors

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

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

21. An efficient diagnosis: A patient with X‐linked inhibitor of apoptosis protein (XIAP) deficiency in the setting of infantile hemophagocytic lymphohistiocytosis was diagnosed using high serum interleukin‐18 combined with common laboratory parameters

22. Case Report: A Case of Epstein-Barr Virus-Associated Acute Liver Failure Requiring Hematopoietic Cell Transplantation After Emergent Liver Transplantation

24. Augmentation of Stimulator of Interferon Genes–Induced Type I Interferon Production in COPA Syndrome

26. Aberrant localization of CDC42 C-terminal variants to the Golgi apparatus drives pyrin inflammasome-dependent autoinflammation

28. Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation

30. Neonatal-onset autoinflammation and immunodeficiency caused by heterozygous missense mutation of the proteasome subunit β-type 9

32. EBV‐associated lymphoproliferative disorder in a patient with X‐linked severe combined immunodeficiency with multiple reversions of an IL2RG mutation in T cells

35. Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the NOD2 mutation

38. Rescue of recurrent deep intronic mutation underlying cell type–dependent quantitative NEMO deficiency

39. A novel NLRP3 variant in two unrelated patients with cryopyrin-associated periodic syndrome

42. Successful treatment of spondyloenchondrodysplasia with baricitinib.

43. Brief Report: Late‐Onset Cryopyrin‐Associated Periodic Syndrome Due to Myeloid‐Restricted Somatic NLRP3 Mosaicism

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