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174 results on '"Karakawa, Shuhei"'

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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

7. Landscape of driver mutations and their clinical effects on Down syndrome–related myeloid neoplasms

11. Scoring system for diagnosis and pretreatment risk assessment of neuroblastoma using urinary biomarker combinations

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

18. Successful Bone Marrow Transplantation in a Patient with Acute Myeloid Leukemia Developed from Severe Congenital Neutropenia Using Modified Chemotherapy and Conditioning Regimen for Leukemia.

19. Human STAT1 gain of function with chronic mucocutaneous candidiasis: A comprehensive review for strengthening the connection between bedside observations and laboratory research.

21. A Pediatric Case of Panniculitis Induced by Pseudomonas AeruginosaWith Clinical Features Similar to Ecthyma Gangrenosum

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

27. Erdafitinib in pediatric patients with advanced solid tumors with fibroblast growth factor receptor (FGFR) gene alterations: RAGNAR study pediatric cohort.

29. Inborn errors of immunity with loss- and gain-of-function germline mutations in STAT1.

31. Successful treatment of BK virus‐associated severe hemorrhagic cystitis with bilateral single‐J ureteral stenting

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

37. Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations

39. A Case Report of a Japanese Boy with Morquio A Syndrome: Effects of Enzyme Replacement Therapy Initiated at the Age of 24 Months

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

45. Successful Hematopoietic Stem Cell Transplantation Using an Immunosuppressive Conditioning Regimen in Ten Patients with Severe Congenital Neutropenia: A Single-Institute Experience

48. Continuous Intravenous Infusion of Ketamine and Lidocaine as Adjuvant Analgesics in a 5-Year-Old Patient with Neuropathic Cancer Pain

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