156 results on '"Hiejima, Eitaro"'
Search Results
2. Clinical outcome of ulcerative colitis with severe onset in children: a multicenter prospective cohort study
3. A Non-targeted Proteomics Newborn Screening Platform for Inborn Errors of Immunity.
4. Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants
5. Efficacy of steroid therapy for improving native liver survival after pediatric acute liver failure with immune activation.
6. Immunophenotyping of A20 haploinsufficiency by multicolor flow cytometry
7. Bruton tyrosine kinase deficiency augments NLRP3 inflammasome activation and causes IL-1[beta]-mediated colitis
8. Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations
9. Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis
10. Successful cord blood transplantation using reduced intensity conditioning in a 5‐month‐old patient with IL‐10RA deficiency.
11. Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations.
12. Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation
13. Alemtuzumab‐based reduced‐intensity conditioning for XIAP deficiency
14. A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients
15. Anti–Integrin αvβ6 Antibody as a Diagnostic Marker for Pediatric Patients With Ulcerative Colitis
16. Assessment of type I interferon signatures in undifferentiated inflammatory diseases: A Japanese multicenter experience
17. Recurrent tandem duplication of UNC13D in familial hemophagocytic lymphohistiocytosis type 3
18. Case Report: A Pediatric Case of Familial Mediterranean Fever Concurrent With Autoimmune Hepatitis
19. Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation
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21. Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report
22. Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation
23. Case Report: A Case of Epstein-Barr Virus-Associated Acute Liver Failure Requiring Hematopoietic Cell Transplantation After Emergent Liver Transplantation
24. Aberrant localization of CDC42 C-terminal variants to the Golgi apparatus drives pyrin inflammasome-dependent autoinflammation
25. Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis
26. Sustained high plasma mannose less sensitive to fluctuating blood glucose in glycogen storage disease type Ia children
27. A Non-targeted Proteomics Newborn Screening Platform for Inborn Errors of Immunity
28. Esophageal foreign body causing sustained stridor in an infant
29. Does the spread of hepatitis B virus genotype A increase the risk of intrafamilial transmission in Japan?
30. Acute lymphoblastic leukemia in a girl with Wilsonʼs disease
31. Gastric ulcer and gastroenteritis caused by Epstein–Barr virus during immunosuppressive therapy for a child with systemic juvenile idiopathic arthritis
32. Acute liver failure in young children with systemic-onset juvenile idiopathic arthritis without macrophage activation syndrome: Report of two cases
33. Source of transmission in children with chronic hepatitis B infection after the implementation of a strategy for prevention in those at high risk
34. Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3
35. Cellular immunity in children with successful immunoprophylactic treatment for mother-to-child transmission of hepatitis B virus
36. Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders
37. 炎症性腸疾患患者ではMucosal-associated invariant T細胞が減少しており、アポトーシスを起こしやすいという特徴がある。
38. A novel NLRP3 variant in two unrelated patients with cryopyrin-associated periodic syndrome
39. Sa2088 Nationwide Multi-Center Study of Pediatric Small Bowel Capsule Endoscopy in Japan
40. Reply to Walsh et al
41. A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients
42. Diagnostic accuracy of endoscopic features of pediatric acute gastrointestinal graft-versus-host disease
43. Reply
44. Reduced Numbers and Proapoptotic Features of Mucosal-associated Invariant T Cells as a Characteristic Finding in Patients with Inflammatory Bowel Disease
45. Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function
46. Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report.
47. Fatty liver and anti-oxidant enzyme activities along with peroxisome proliferator-activated receptors γ and α expressions in the liver of Wilson's disease
48. Sustained high plasma mannose less sensitive to fluctuating blood glucose in glycogen storage disease type Ia children
49. Acute liver failure in young children with systemic-onset juvenile idiopathic arthritis without macrophage activation syndrome: Report of two cases
50. Utility of Simplified Criteria for the Diagnosis of Autoimmune Hepatitis in Children
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