128 results on '"Sasahara, Yoji"'
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2. Clofarabine monotherapy in two patients with refractory Langerhans cell histiocytosis
3. Challenges to Widespread Use of Fertility Preservation Facilities for Pediatric Cancer Patients in Japan
4. Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity
5. Two‐year crizotinib monotherapy induced durable complete response of pediatric ALK‐positive inflammatory myofibroblastic tumor
6. Factors associated with employment status among mothers of survivors of childhood cancer: a cross-sectional study
7. Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome
8. Living Donor Lobar Lung Transplant for a Patient With Lung Disease Caused by ABCA3 Gene Mutations: A Case Report
9. Comprehensive genomic profiling suggested multifocal development of retinoblastoma in a single eye
10. Anti–Integrin αvβ6 Antibody as a Diagnostic Marker for Pediatric Patients With Ulcerative Colitis
11. Stage M Infantile Neuroblastoma With Involvement of Falx Cerebri: Case Report and Literature Review
12. Phenotypic heterogeneity in individuals with MECOM variants in 2 families
13. Impairment of cytokine production following immunological synapse formation in patients with Wiskott-Aldrich syndrome and leukocyte adhesion deficiency type 1
14. Intraoperative Placement of an Absorbable Spacer Prior to Radiation Therapy for a Malignant Peripheral Nerve Sheath Tumor
15. NovelPOLEmutations identified in patients with IMAGE-I syndrome cause aberrant subcellular localisation and protein degradation in the nucleus
16. Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation
17. Registry data analysis of hematopoietic stem cell transplantation on systemic chronic active Epstein–Barr virus infection patients in Japan
18. A pediatric case of osteosarcoma and tuberous sclerosis complex with a novel germline mutation in the TSC2 gene and a somatic mutation in the TP53 gene
19. BRAF V600E-positive cells as molecular markers of bone marrow disease in pediatric Langerhans cell histiocytosis
20. Primary Immunodeficiencies Associated With Early-Onset Inflammatory Bowel Disease in Southeast and East Asia
21. Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985–2016
22. The Work Experienced in Fostering Posttraumatic Growth Among Parents of Children with Leukemia: A Qualitative Study Using a Modified Grounded Theory Approach
23. The Outcomes of Systemic Chronic Active EBV Infection Treatment By Allogeneic Hematopoietic Stem Cell Transplantation: An Analysis of Japanese Registry Data
24. Clofarabine monotherapy in two patients with refractory Langerhans cell histiocytosis
25. Hematopoietic Cell Transplantation Rescues Inflammatory Bowel Disease and Dysbiosis of Gut Microbiota in XIAP Deficiency
26. Aberrant localization of CDC42 C-terminal variants to the Golgi apparatus drives pyrin inflammasome-dependent autoinflammation
27. Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study
28. Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia–telangiectasia caused by novel compound heterozygous variants in ATM
29. Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation
30. Catecholamine‐induced paralytic ileus controlled by phentolamine in a child with giant differentiating neuroblastoma
31. Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other Than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985–2016
32. Chronological changes of skin eruptions toward cold abscess formation in hyper‐immunoglobulin E syndrome
33. Pediatric psoriasis induced by HLA‐B46‐Cw1 haplotype: A retrospective study of psoriasis onset after hematopoietic stem cell transplantation
34. Case Report: Infantile-Onset Fulminant Type 1 Diabetes Mellitus Caused by Novel Compound Heterozygous LRBA Variants
35. A pediatric case of osteosarcoma and tuberous sclerosis complex with a novel germline mutation in the TSC2 gene and a somatic mutation in the TP53 gene
36. The Working Group for Revision of “Guidelines for the Use of Palivizumab in Japan”: A Committee Report
37. Correction: Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia
38. Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond–Blackfan anemia
39. Chemoradiotherapy of spinal extradural Ewing sarcoma after the Fontan procedure
40. Utility of a bridged nucleic acid clamp for liquid biopsy: Detecting BRAF V600E in the cerebrospinal fluid of a patient with brain tumor
41. Comprehensive Targeted Sequencing Identifies Monogenic Disorders in Patients With Early-onset Refractory Diarrhea
42. Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation
43. The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation
44. Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation
45. Improvement of native pulmonary alveolar proteinosis after contralateral single living‐donor lobar lung transplantation: A case report
46. Elucidation of the Effects of a Current X-SCID Therapy on Intestinal Lymphoid Organogenesis Using an In Vivo Animal Model
47. Hematopoietic stem cell transplantation for pediatric acute myeloid leukemia patients with KMT2A rearrangement; A nationwide retrospective analysis in Japan
48. Atopic dermatitis without serum immunoglobulin E elevation or loss‐of‐function filaggrin gene mutation in a patient with X‐linked agammaglobulinemia
49. 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
50. BRAFV600E-Positive Precursors As Molecular Markers of Bone Marrow Involvement in Pediatric Langerhans Cell Histiocytosis
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