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1. Pharmacokinetics, safety, and efficacy of 20% subcutaneous immunoglobulin (Ig20Gly) administered weekly or every 2 weeks in Japanese patients with primary immunodeficiency diseases: a phase 3, open-label study.

3. Immunological profile in a family with nephrogenic diabetes insipidus with a novel 11 kb deletion in AVPR2 and ARHGAP4 genes

4. Large scale analysis of pediatric antiviral CD8+ T cell populations reveals sustained, functional and mature responses

10. Hemophagocytic Lymphohistiocytosis in Children with Chronic Granulomatous Disease—Single-Center Experience from North India

15. Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency

16. Corrigendum: Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency

17. qMaLioffG: A single green fluorescent protein FLIM indicator enabling quantitative imaging of endogenous ATP

19. A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside

21. Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency

23. Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency

24. Clinical and Immunological Characterization of ICF Syndrome in Japan

27. A complementary approach for genetic diagnosis of inborn errors of immunity using proteogenomic analysis

28. Successful Treatment of Granulomatous-lymphocytic Interstitial Lung Disease in a Patient with CTLA-4 Deficiency

31. Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study

34. Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies

36. Common Variable Immunodeficiency Caused by FANC Mutations

37. Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy

41. Meningoencephalitis in primary antibody deficiency: Our experience from northwest India

44. Decreased somatic hypermutation induces an impaired peripheral B cell tolerance checkpoint

45. Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015

46. The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies

47. Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism

50. Outcomes of Childhood Pulmonary Arterial Hypertension in BMPR2 and ALK1 Mutation Carriers

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