290 results on '"Nishikomori R."'
Search Results
2. High level of serum human interleukin-18 in a patient with pyogenic arthritis, pyoderma gangrenosum and acne syndrome
3. Obvious optic disc swelling in a patient with cryopyrin-associated periodic syndrome
4. Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen
5. Diagnosis of NLRP3 somatic mosaicism in CINCA/NOMID patients using next-generation sequencing
6. Clinical heterogeneity among a three-generation Japanese family with D18N TREX1 mutation for Aicardi-Goutières syndrome / familial chilblain lupus
7. Dosing patterns of canakinumab in patients with Cryopyrin-Associated Periodic Syndromes (CAPS): A comparative analysis of a study in Western versus Japanese patients
8. Reply
9. Guidelines for the genetic diagnosis of hereditary recurrent fevers
10. Thymus hyperplasia in a girl undergoing treatment with tocilizumab for systemic juvenile idiopathic arthritis: 703284
11. DOHaD and Allergic Diseases in Schoolchildren: Does IUGR Affect Risk of Allergic Diseases?: 719
12. Birth Order Effect on the Prevalence of Childhood Allergy: Comparisons among Different Allergic Diseases: 525
13. Functional analysis of a novel G87V TNFRSF1A mutation in patients with TNF receptor-associated periodic syndrome
14. Evidence-based provisional clinical classification criteria for autoinflammatory periodic fevers
15. 5326Can patient-derived iPSCs be applied to phenotypic cell-based high throughput screening assessment to distinguish between different types of long-QT syndrome?
16. A sporadic case of granulomatous disease negative for NOD2 mutations and mimicking Blau syndrome
17. Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency
18. AB0995 Clinical, therapeutic, and genetic analyses in a patient with papa syndrome complicated with inflammatory bowel disease
19. High level of serum human interleukin-18 in a patient with pyogenic arthritis, pyoderma gangrenosum and acne syndrome
20. Remarkable improvement of articular pain by biologics in a Multicentric carpotarsal osteolysis patient with a mutation of MAFB gene
21. Clinical and genetic analyses in a patient with PAPA syndrome complicated with inflammatory bowel disease
22. Understanding the pathophysiology of NOMID arthropathy for drug discovery by iPSCs technology
23. Remarkable improvement of articular pain by biologics in a Multicentric carpotarsal osteolysis patient with a mutation of MAFB gene.
24. Understanding the pathophysiology of NOMID arthropathy for drug discovery by iPSCs technology
25. Clinical and genetic analyses in a patient with PAPA syndrome complicated with inflammatory bowel disease
26. Somatic NLRP3 mosaicism in Muckle-Wells syndrome
27. STAT4 serine phosphorylation is critical for IL-12-induced IFN-W production but not for cell proliferation
28. STAT4 serine phosphorylation is critical for IL-12-induced IFN-? production but not for cell proliferation
29. STAT4 serine phosphorylation is critical for IL-12 induced IFN-gamma production and Th1 differentiation
30. A nationwide survey of Aicardi-Goutieres syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study
31. P03-023 – Autoinflammatory diseases database in Japan
32. PW02-029 - Single cell fluorescent immunoassay of CINCA/NOMID
33. A Japanese pediatric patient with coexisting systemic lupus erythematosus and familial Mediterranean fever
34. Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi-Goutieres syndrome/familial chilblain lupus
35. Gastric ulcer and gastroenteritis caused by Epstein-Barr virus during immunosuppressive therapy for a child with systemic juvenile idiopathic arthritis
36. Detection of Base Substitution-Type Somatic Mosaicism of the NLRP3 Gene with >99.9% Statistical Confidence by Massively Parallel Sequencing
37. Cryopyrin-associated Periodic Syndrome: A Case Report and Review of the Japanese Literature
38. Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency.
39. The CD40-CD40L axis and IFN- play critical roles in Langhans giant cell formation
40. Clinical heterogeneity among a three-generation Japanese family with D18N TREX1 mutation for Aicardi-Goutières syndrome / familial chilblain lupus
41. Dosing patterns of canakinumab in patients with Cryopyrin-Associated Periodic Syndromes (CAPS): A comparative analysis of a study in Western versus Japanese patients
42. Diagnosis of NLRP3 somatic mosaicism in CINCA/NOMID patients using next-generation sequencing
43. Screening of Untreated Schoolchildren with Allergic Symptoms - How many are left untreated?
44. Total and LDL Cholesterol Are Associated with Atopic Status in Schoolchildren
45. Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15
46. Breast-feeding in Infancy and the Prevalence of Allergic Diseases in Schoolchildren-Does Reverse Causation Matter?
47. Growth Of Schoolchildren With Food Allergy To Egg, Milk, Or Wheat In Infancy
48. Allergic Status of Schoolchildren with Food Allergy to Egg, Milk or Wheat in Infancy
49. Childhood Obesity as a Possible Aggravating Factor of Atopic Dermatitis
50. SPINK5 polymorphism and disease severity among Japanese children with atopic dermatitis
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