308 results on '"Sasahara, Yoji"'
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2. Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood
3. Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome
4. Factors associated with employment status among mothers of survivors of childhood cancer: a cross-sectional study
5. Living Donor Lobar Lung Transplant for a Patient With Lung Disease Caused by ABCA3 Gene Mutations: A Case Report
6. Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985–2016
7. Comprehensive genetic analysis for identification of monogenic disorders and selection of appropriate treatments in pediatric patients with persistent thrombocytopenia.
8. Favorable prognosis of vaccine-associated immune thrombocytopenia in children is correlated with young age at vaccination: Retrospective survey of a nationwide disease registry
9. Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia–telangiectasia caused by novel compound heterozygous variants in ATM
10. Mechanisms of genotype-phenotype correlation in autosomal dominant anhidrotic ectodermal dysplasia with immune deficiency
11. Hematopoietic Cell Transplantation Rescues Inflammatory Bowel Disease and Dysbiosis of Gut Microbiota in XIAP Deficiency
12. Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study
13. Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond–Blackfan anemia
14. Elucidation of the Effects of a Current X-SCID Therapy on Intestinal Lymphoid Organogenesis Using an In Vivo Animal Model
15. Hematopoietic stem cell transplantation for pediatric acute myeloid leukemia patients with KMT2A rearrangement; A nationwide retrospective analysis in Japan
16. Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation
17. Clinical practice recommendations for the diagnosis and management of human herpesvirus-6B encephalitis after allogeneic hematopoietic stem cell transplantation: the Japan Society for Hematopoietic Cell Transplantation
18. Efficacy of rituximab for the treatment and prevention of autoimmunity in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia
19. The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation
20. Comprehensive Targeted Sequencing Identifies Monogenic Disorders in Patients With Early-onset Refractory Diarrhea
21. Impact of low-dose irradiation and in vivo T-cell depletion on hematopoietic stem cell transplantation for non-malignant diseases using fludarabine-based reduced-intensity conditioning
22. Hematopoietic stem cell transplantation in children and adolescents with relapsed or refractory B-cell non-Hodgkin lymphoma
23. Wiskott-Aldrich Syndrome Protein Is Required for NK Cell Cytotoxicity and Colocalizes with Actin to NK Cell-Activating Immunologic Synapses
24. Infantile-onset inflammatory bowel disease in a patient with Hermansky-Pudlak syndrome: a case report
25. Correction: Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia
26. IKBA S32 Mutations Underlie Ectodermal Dysplasia with Immunodeficiency and Severe Noninfectious Systemic Inflammation
27. Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan
28. Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study
29. Allogeneic Hematopoietic Stem Cell Transplantation for Leukocyte Adhesion Deficiency
30. Phenotypic heterogeneity in individuals with MECOM variants in 2 families
31. Impairment of cytokine production following immunological synapse formation in patients with Wiskott-Aldrich syndrome and leukocyte adhesion deficiency type 1
32. Casitas B-cell lymphoma mutation in childhood T-cell acute lymphoblastic leukemia
33. Refractory atopic dermatitis in a child with hypomorphic mutation in XIAP gene and low serum IgG.
34. WIP Is a Chaperome for Wiskott-Aldrich Syndrome Protein (WASP)
35. Identification of acquired mutations by whole-genome sequencing in GATA-2 deficiency evolving into myelodysplasia and acute leukemia
36. Hematopoietic stem cell transplantation for inborn errors of metabolism: A report from the Research Committee on Transplantation for Inborn Errors of Metabolism of the Japanese Ministry of Health, Labour and Welfare and the Working Group of the Japan Society for Hematopoietic Cell Transplantation
37. WASP–WIP complex in the molecular pathogenesis of Wiskott–Aldrich syndrome
38. Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets
39. Identification of novel kinase fusion transcripts in paediatric B cell precursor acute lymphoblastic leukaemia with IKZF1 deletion
40. Recurrent pneumonia with mild hypogammaglobulinemia diagnosed as X-linked agammaglobulinemia in adults
41. Two‐year crizotinib monotherapy induced durable complete response of pediatric ALK‐positive inflammatory myofibroblastic tumor.
42. B-cell function after unrelated umbilical cord blood transplantation using a minimal-intensity conditioning regimen in patients with X-SCID
43. Interstitial lung disease in two brothers with novel compound heterozygous ABCA3 mutations
44. Nationwide Survey of Patients with Primary Immunodeficiency Diseases in Japan
45. Mesenchymal chondrosarcoma diagnosed on FISH for HEY1-NCOA2 fusion gene
46. The open conformation of WASP regulates its nuclear localization and gene transcription in myeloid cells
47. A nationwide survey of Aicardi–Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study
48. IDH2 and TP53 mutations are correlated with gliomagenesis in a patient with Maffucci syndrome
49. Selective expansion of donor-derived regulatory T cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome
50. Clofarabine monotherapy in two patients with refractory Langerhans cell histiocytosis.
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