196 results on '"Kobayashi, Norimoto"'
Search Results
2. Mosaicism of an ELANE Mutation in an Asymptomatic Mother
3. Analysis of biomarker serum levels in IVIG and infliximab refractory Kawasaki disease patients
4. In-depth proteomic analysis of juvenile dermatomyositis serum reveals protein expression associated with muscle-specific autoantibodies
5. A low-frequency IL4R locus variant in Japanese patients with intravenous immunoglobulin therapy-unresponsive Kawasaki disease
6. Early diagnosis of early-onset sarcoidosis: a case report with functional analysis and review of the literature
7. Markedly elevated CD64 expression on neutrophils and monocytes as a biomarker for diagnosis and therapy assessment in Kawasaki disease
8. Acute Myeloid Leukemia in a Patient With X-linked Severe Combined Immunodeficiency
9. IFR4/MUM1‐positive lymphoma in Waldeyer ring with co‐expression of CD5 and CD10
10. Immune Complex-Mediated Glomerulonephritis in a Patient with Wiskott–Aldrich Syndrome
11. Clinical Course in a Patient With Neutrophil-Specific Granule Deficiency and Rapid Detection of Neutrophil Granules as a Screening Test
12. Serial monitoring of Mucorales DNA load in serum samples of a patient with disseminated mucormycosis after allogeneic bone marrow transplantation
13. Markedly elevated CD64 expressions on neutrophils and monocytes are useful for diagnosis of periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome during flares
14. Cytomegalovirus Encephalitis in a Patient with Severe Combined Immunodeficiency
15. Dramatic Improvement in the Multifocal Positron Emission Tomography Findings of a Young Adult with Chronic Granulomatous Disease Following Allogeneic Hematopoietic Stem Cell Transplantation
16. Clinical and laboratory features of fatal rapidly progressive interstitial lung disease associated with juvenile dermatomyositis
17. Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes
18. Successful treatment for West syndrome with severe combined immunodeficiency
19. Successful cord blood transplantation after repeated transfusions of unmobilized neutrophils in addition to antifungal treatment in an infant with chronic granulomatous disease complicated by invasive pulmonary aspergillosis
20. Clinical impact of myositis-specific autoantibodies on long-term prognosis of juvenile idiopathic inflammatory myopathies: multicentre study
21. Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families
22. Food allergy after cord blood transplantation in children
23. Clinical practice guidance for juvenile dermatomyositis (JDM) 2018-Update
24. Identification of Severe Combined Immunodeficiency by T-Cell Receptor Excision Circles Quantification Using Neonatal Guthrie Cards
25. TIM-1 and TIM-4 Glycoproteins Bind Phosphatidylserine and Mediate Uptake of Apoptotic Cells
26. CD30+ anaplastic large cell lymphoma complicated by pyoderma gangrenosum with increased levels of serum cytokines
27. Neutrophil-mediated inflammation in respiratory syncytial viral bronchiolitis
28. Expansion of clonotype-restricted HLA-identical maternal CD4 + T cells in a patient with severe combined immunodeficiency and a homozygous mutation in the Artemis gene
29. A Pediatric Case of Relapsing-Remitting Multiple Sclerosis Onset following Varicella Zoster Ophthalmicus with Optic Neuritis
30. Clinical features and new diagnostic criteria for the syndrome of periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis
31. Absence of Memory B Cells in Patients with Common Variable Immunodeficiency
32. The different process of class switching and somatic hypermutation; a novel analysis by CD27− naive B cells
33. Heterozygous Mutations in OAS1 Cause Infantile-Onset Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia
34. External validation of the EULAR/ACR idiopathic inflammatory myopathies classification criteria with a Japanese paediatric cohort.
35. Heterozygous Mutations in OAS1 Cause Infantile-Onset Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia
36. Analysis of serum IL-38 in juvenile-onset systemic lupus erythematosus
37. Infliximab versus intravenous immunoglobulin for refractory Kawasaki disease: a phase 3, randomized, open-label, active-controlled, parallel-group, multicenter trial
38. Characteristics and outcome of intractable vasculitis syndrome in children: Nation-wide survey in Japan
39. IFR4/MUM1-positive lymphoma in Waldeyer ring with co-expression of CD5 and CD10
40. Novel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's disease
41. Neurological Course of a Surviving Infant With Cytomegalovirus Ventriculoencephalitis and Polyradiculomyelitis
42. Increased Serum B Cell Activating Factor and a Proliferation-inducing Ligand Are Associated with Interstitial Lung Disease in Patients with Juvenile Dermatomyositis
43. A novel surfactant protein C L55F mutation associated with interstitial lung disease alters subcellular localization of proSP-C in A549 cells
44. An Increase in Circulating B Cell–Activating Factor in Childhood-Onset Ocular Myasthenia Gravis
45. Successful treatment for West syndrome with severe combined immunodeficiency
46. IL-18 serum concentration is markedly elevated in typical familial Mediterranean fever with M694I mutation and can distinguish it from atypical type
47. Dramatic Improvement in the Multifocal Positron Emission Tomography Findings of a Young Adult with Chronic Granulomatous Disease Following Allogeneic Hematopoietic Stem Cell Transplantation
48. SomaticNLRP3mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes
49. Successful cord blood transplantation after repeated transfusions of unmobilized neutrophils in addition to antifungal treatment in an infant with chronic granulomatous disease complicated by invasive pulmonary aspergillosis
50. Increased Serum B Cell Activating Factor and a Proliferation-inducing Ligand Are Associated with Interstitial Lung Disease in Patients with Juvenile Dermatomyositis.
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