38 results on '"Nonoyama Shigeaki"'
Search Results
2. Neuroprotective effects of adenosine deaminase in the striatum
3. Clinical features and hematopoietic stem cell transplantations for CD40 ligand deficiency in Japan
4. Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies
5. Maternal mosaicism of an ANKH mutation in a family with craniometaphyseal dysplasia
6. Factors Associated with Steroid Phobia in Caregivers of Children with Atopic Dermatitis
7. Salivary Cortisol Response to Stress in Young Children with Atopic Dermatitis
8. Endocrine complications in primary immunodeficiency diseases in Japan
9. Multiple Reversions of an IL2RG Mutation Restore T cell Function in an X-linked Severe Combined Immunodeficiency Patient
10. Hyper-eosinophilia in granular acute B-cell lymphoblastic leukemia with myeloid antigen expression
11. Clinical and Genetic Characteristics of XIAP Deficiency in Japan
12. Nationwide Survey of Patients with Primary Immunodeficiency Diseases in Japan
13. Analysis of somatic hypermutations in the IgM switch region in human B cells
14. Hemophagocytosis after bone marrow transplantation for JAK3-deficient severe combined immunodeficiency
15. Rapidly progressive encephalopathy with coagulation abnormality (Discussion and Diagnosis)
16. Rapidly progressive encephalopathy with coagulation abnormality (Case Presentation)
17. Quantitative assessment of PTPN11 or RAS mutations at the neonatal period and during the clinical course in patients with juvenile myelomonocytic leukaemia
18. A case of glycogen storage disease type Ib presenting with prolonged neonatal hypoglycaemia and minimal metabolic abnormalities
19. Identification of Severe Combined Immunodeficiency by T-Cell Receptor Excision Circles Quantification Using Neonatal Guthrie Cards
20. Primary immunodeficiencies: 2009 update
21. Two Brothers with Ataxia-Telangiectasia-like Disorder with Lung Adenocarcinoma
22. RAPID: Resource of Asian Primary Immunodeficiency Diseases
23. Soluble TWEAK is markedly elevated in hemophagocytic lymphohistiocytosis
24. Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
25. dup(8p)/del(8q) Recombinant Chromosome in a Girl With Hepatic Focal Nodular Hyperplasia
26. Bone Marrow Transplantation From a Pediatric Donor With a High Frequency of Cytomegalovirus-Specific T-Cells
27. Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity
28. Outcome in patients with Wiskott–Aldrich syndrome following stem cell transplantation: an analysis of 57 patients in Japan
29. A Non-Obese Boy With Prader-Willi Syndrome Shows Cardiopulmonary Impairment Due to Severe Kyphoscoliosis
30. Analysis of serum soluble CD40 ligand (sCD40L) in the patients undergoing allogeneic stem cell transplantation: platelet is a major source of serum sCD40L
31. Common variable immunodeficiency classification by quantifying T-cell receptor and immunoglobulin κ-deleting recombination excision circles
32. X-linked thrombocytopenia in a girl
33. Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects
34. WASP is involved in proliferation and differentiation of human haemopoietic progenitors in vitro
35. Absence of IgD- CD27+ Memory B Cell Population in X-linked Hyper-IgM Syndrome
36. Diminished Expression of CD40 Ligand by Activated Neonatal T Cells
37. The Random Inactivation of the X Chromosome Carrying the Defective Gene Responsible for X-linked Hyper IgM Syndrome (X-HIM) in Female Carriers of HIGM1
38. Activated B Cells from Patients with Common Variable Immunodeficiency Proliferate and Synthesize Immunoglobulin
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