167 results on '"Honda, Yoshitaka"'
Search Results
2. Partial Trisomy 9p with Clinical Symptoms Resembling Interferonopathies
3. Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants
4. Hematopoietic Cell Transplantation Ameliorates Autoinflammation in A20 Haploinsufficiency
5. Necrotizing Funisitis as an Intrauterine manifestation of Cryopyrin-Associated Periodic Syndrome: a case report and review of the literature
6. A novel mutation in early‐onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes
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
9. Successful cord blood transplantation using reduced intensity conditioning in a 5‐month‐old patient with IL‐10RA deficiency.
10. Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity
11. Incomplete Presentation of WHIM Syndrome: The Diagnostic Role of Dysmorphic Neutrophils in Bone Marrow
12. The Environmental Degradability of Demnum, a Typical Pfpe Polymer
13. Trial of rotor balancing for acoustic response reduction in automotive motors
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
17. Functional Components and Health Benefits of Fermented Soymilk
18. Case Report: A Pediatric Case of Familial Mediterranean Fever Concurrent With Autoimmune Hepatitis
19. Induced Pluripotent Stem Cell-Derived Monocytes/Macrophages in Autoinflammatory Diseases
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
23. Allograft Dysfunction After Lung Transplantation for COPA Syndrome: A Case Report and Literature Review
24. Augmentation of Stimulator of Interferon Genes–Induced Type I Interferon Production in COPA Syndrome
25. Partial Trisomy 9p with Clinical Symptoms Resembling Interferonopathies
26. Aberrant localization of CDC42 C-terminal variants to the Golgi apparatus drives pyrin inflammasome-dependent autoinflammation
27. 深部イントロン変異による細胞種依存性量的NEMO異常症の病態解明と低分子化合物による治療の試み
28. Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation
29. Febrile attacks triggered by milk allergy in an infant with mevalonate kinase deficiency
30. Neonatal-onset autoinflammation and immunodeficiency caused by heterozygous missense mutation of the proteasome subunit β-type 9
31. Glycemic variability in preterm infants receiving intermittent gastric tube feeding: Report of three cases
32. EBV‐associated lymphoproliferative disorder in a patient with X‐linked severe combined immunodeficiency with multiple reversions of an IL2RG mutation in T cells
33. Necrotizing Funisitis As an Intrauterine Manifestation of Cryopyrin-Associated Periodic Syndrome: A Case Report and Review of The Literature
34. Successful treatment of spondyloenchondrodysplasia with baricitinib
35. Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the NOD2 mutation
36. Pyoderma gangrenosum associated with chronic recurrent multifocal osteomyelitis as a possible paradoxical reaction to anti‐tumor necrosis factor‐α therapy
37. Haploinsufficiency of A20 with a novel mutation of deletion of exons 2–3 of TNFAIP3
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
40. A Case with Spondyloenchondrodysplasia Treated with Growth Hormone
41. Vaccine-strain herpes zoster found in the trigeminal nerve area in a healthy child: A case report
42. Successful treatment of spondyloenchondrodysplasia with baricitinib.
43. Brief Report: Late‐Onset Cryopyrin‐Associated Periodic Syndrome Due to Myeloid‐Restricted Somatic NLRP3 Mosaicism
44. A case of neonatal toxic shock syndrome-like exanthematous disease concurrent with maternal toxic shock syndrome
45. Characterization of Soymilk Prepared by Ohmic Heating and the Effects of Voltage Applied
46. パルスレーザー堆積法によるMgO(100)薄膜のホモエピタキシャル成長
47. Interface Engineering of MgO and Al2O3 by Pulsed Laser Deposition
48. MgO 超薄膜のX線光電子分光
49. 静電不安定性を持つMgO(111)超薄膜の作製と評価
50. Determination of α-hydroxy acids and their enantiomers in fruit juices by ligand exchange CE with a dual central metal ion system
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