180 results on '"Karakawa, Shuhei"'
Search Results
2. Correction to: Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency
3. Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency
4. Eculizumab treatment in paediatric patients diagnosed with aHUS after haematopoietic stem cell transplantation: a HSCT-TMA case series from Japanese aHUS post-marketing surveillance
5. Clinical significance of human neutrophil antigen-1 antibodies in children with neutropenia
6. A PEDIATRIC CASE OF PANNICULITIS INDUCED BY Pseudomonas aeruginosa WITH CLINICAL FEATURES SIMILAR TO ECTHYMA GANGRENOSUM
7. Isolated Chronic Mucocutaneous Candidiasis due to a Novel Duplication Variant of IL17RC
8. Landscape of driver mutations and their clinical effects on Down syndrome–related myeloid neoplasms
9. Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
10. Successful Hematopoietic Stem Cell Transplantation for Autosomal Recessive STAT1 Complete Deficiency
11. Scoring system for diagnosis and pretreatment risk assessment of neuroblastoma using urinary biomarker combinations
12. Intravenous Thrombolysis for Pediatric Ischemic Stroke Secondary to Cancer Therapy-related Cardiac Dysfunction: A Case Report
13. Retrospective Evaluation of an Oral Propranolol Delivery Strategy in 25 Cases of Infantile Hemangioma
14. Isolated Chronic Mucocutaneous Candidiasis due to a Novel Duplication Variant of IL17RC
15. Eculizumab treatment in paediatric patients diagnosed with aHUS after haematopoietic stem cell transplantation: a HSCT-TMA case series from Japanese aHUS post-marketing surveillance
16. Myeloid/natural killer (NK) cell precursor acute leukemia as a distinct leukemia type
17. Human STAT1 gain of function with chronic mucocutaneous candidiasis: A comprehensive review for strengthening the connection between bedside observations and laboratory research
18. Neutropenia (In Infancy and Childhood)
19. Human STAT1 gain of function with chronic mucocutaneous candidiasis: A comprehensive review for strengthening the connection between bedside observations and laboratory research.
20. Successful Bone Marrow Transplantation in a Patient with Acute Myeloid Leukemia Developed from Severe Congenital Neutropenia Using Modified Chemotherapy and Conditioning Regimen for Leukemia.
21. A Pediatric Case of Panniculitis Induced by Pseudomonas AeruginosaWith Clinical Features Similar to Ecthyma Gangrenosum
22. Primäre Autoimmunneutropenie im Säuglings‐ und Kindesalter mit Hautinfektion
23. Chronic Neutropenia in Children With Abscess Forming Cervical Lymphadenitis Caused by Staphylococcus aureus
24. A complementary approach for genetic diagnosis of inborn errors of immunity using proteogenomic analysis
25. Primary autoimmune neutropenia in infancy and childhood accompanied by cutaneous infection
26. Inborn errors of immunity with loss- and gain-of-function germline mutations in STAT1
27. Anti‐human neutrophil antigen‐1a, ‐1b, and ‐2 antibodies in neonates and children with immune neutropenias analyzed by extracted granulocyte antigen immunofluorescence assay
28. Inborn errors of immunity with loss- and gain-of-function germline mutations in STAT1.
29. Mosaicism of an ELANE Mutation in an Asymptomatic Mother in a Familial Case of Cyclic Neutropenia
30. Erdafitinib in pediatric patients with advanced solid tumors with fibroblast growth factor receptor (FGFR) gene alterations: RAGNAR study pediatric cohort.
31. Successful treatment of BK virus‐associated severe hemorrhagic cystitis with bilateral single‐J ureteral stenting
32. A pediatric case of congenital neutropenia with SRP54 gene mutation in which monocytosis and gingival swelling were useful in differentiating from autoimmune neutropenia
33. Decreased Expression in Nuclear Factor-κB Essential Modulator Due to a Novel Splice-Site Mutation Causes X-linked Ectodermal Dysplasia with Immunodeficiency
34. T2-FLAIR Mismatch Sign and Response to Radiotherapy in Diffuse Intrinsic Pontine Glioma
35. Comprehensive Genetic Analysis Revealed Myeloid/Natural Killer (NK) Cell Precursor Acute Leukemia As a Novel Distinctive Leukemia Entity
36. Possible involvement of regulatory T cell abnormalities and variational usage of TCR repertoire in children with autoimmune neutropenia
37. Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations
38. Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia
39. A Case Report of a Japanese Boy with Morquio A Syndrome: Effects of Enzyme Replacement Therapy Initiated at the Age of 24 Months
40. Mediastinal hemangiopericytoma
41. Successful Bone Marrow Transplantation Using an Immunomyelosuppressive Conditioning in Patients with Severe Congenital Neutropenia: The Results of a Single-Institute
42. Clinical Feature and Genetic Alterations in Myeloid/Natural Killer (NK) Cell Precursor Acute Leukemia and Myeloid/NK Cell Acute Leukemia
43. Adult-onset primary cyclic autoimmune neutropenia: a case report
44. Azacitidine successfully maintained the second remission in an infant with KMT2A -rearranged acute lymphoblastic leukemia who relapsed after unrelated cord blood transplantation
45. Successful Hematopoietic Stem Cell Transplantation Using an Immunosuppressive Conditioning Regimen in Ten Patients with Severe Congenital Neutropenia: A Single-Institute Experience
46. Long-Term Follow-up of Patients with Chronic Granulomatous Disease Receiving Bone Marrow Transplantation Using Immunosuppressive Conditioning Regimen
47. Successful Retransplantation of Bone Marrow Cells Following Failure of Initial Engraftment in 4 Patients with SCN
48. Erythropoietin Treatment Enhanced Cell Surface CXCR4 Expression On Neonatal CD34-Positive Cells
49. Continuous Intravenous Infusion of Ketamine and Lidocaine as Adjuvant Analgesics in a 5-Year-Old Patient with Neuropathic Cancer Pain
50. Clinical and Genetic Characteristics of Patients with Severe Congenital Neutropenia in Japan,
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.