SHUHEI KARAKAWA

Last Updated :2023/11/02

Affiliations, Positions
Hiroshima University Hospital(Medical), Assistant Professor
E-mail
kara1224hiroshima-u.ac.jp

Basic Information

Academic Degrees

  • Doctor of Philosophy in Medical Science, Hiroshima University

Research Fields

  • Medicine,dentistry, and pharmacy;Clinical internal medicine;Pediatrics

Educational Activity

Course in Charge

  1. 2023, Undergraduate Education, Year, Systemic Disease Control
  2. 2023, Undergraduate Education, Intensive, Practice of Medicine I
  3. 2023, Undergraduate Education, Intensive, Practice of Medicine II
  4. 2023, Undergraduate Education, 2Term, Pediatrics
  5. 2023, Undergraduate Education, 2Term, Pediatrics

Research Activities

Academic Papers

  1. A pediatric case of congenital neutropenia with SRP54 gene mutation in which monocytosis and gingival swelling were useful in differentiating from autoimmune neutropenia, Pediatr Blood Cancer, 20220306
  2. Successful treatment of BK virus-associated severe hemorrhagic cystitis with bilateral single-J ureteral stenting, International Journal of Urology, 20220426
  3. Disseminated Aspergillus siamensis infection following haploidentical bone marrow transplantation for chronic granulomatous disease, Rinsho Ketsueki, 61(4), 327-333, 20200501
  4. Transient pseudothrombocytopenia in a neonate: Transmission of a maternal EDTA-dependent anticoagulant, PLATELETS, 23(5), 399-400, 2012
    Link to Paper Search Results by DOI
  5. Mosaicism of an ELANE Mutation in an Asymptomatic Mother in a Familial Case of Cyclic Neutropenia, JOURNAL OF CLINICAL IMMUNOLOGY, 35(5), 512-516, 2015
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  6. Reconstitution of Regulatory T Cells Involves in the Development of Acute Graft-Versus-Host Disease after Hematopoietic Stem Cell Transplantation., BLOOD, 112(11), 769-769, 2008
  7. Decreased Expression in Nuclear Factor-kappa B Essential Modulator Due to a Novel Splice-Site Mutation Causes X-linked Ectodermal Dysplasia with Immunodeficiency, JOURNAL OF CLINICAL IMMUNOLOGY, 31(5), 762-772, 2011
  8. Clinical and Genetic Characteristics of Patients with Severe Congenital Neutropenia in Japan, BLOOD, 118(21), 1387-1388, 2011
  9. Erythropoietin Treatment Enhanced Cell Surface CXCR4 Expression On Neonatal CD34-Positive Cells, BLOOD, 120(21), 2012
  10. Successful Retransplantation of Bone Marrow Cells Following Failure of Initial Engraftment in 4 Patients with SCN, BLOOD, 124(21), 2014
  11. Azacitidine successfully maintained the second remission in an infant with KMT2A-rearranged acute lymphoblastic leukemia who relapsed after unrelated cord blood transplantation, Pediatric Blood and Cancer, 20170704
  12. Azacitidine successfully maintained the second remission in an infant with KMT2A-rearranged acute lymphoblastic leukemia who relapsed after unrelated cord blood transplantation, PEDIATRIC BLOOD & CANCER, 64(12), 201712
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  13. Anti-human neutrophil antigen-1a,-1b, and-2 antibodies in neonates and children with immune neutropenias analyzed by extracted granulocyte antigen immunofluorescence assay, TRANSFUSION, 57(11), 2586-2594, 201711
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  14. Adult-onset primary cyclic autoimmune neutropenia: a case report, TRANSFUSION, 58(4), 884-890, 201804
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  15. Simultaneous detection of ABL1 mutation and IKZF1 deletion in Philadelphia chromosome-positive acute lymphoblastic leukemia using a customized target enrichment system panel, INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 40(4), 427-436, 201808
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  16. Chronic Neutropenia in Children With Abscess Forming Cervical Lymphadenitis Caused by Staphylococcus aureus, PEDIATRIC INFECTIOUS DISEASE JOURNAL, 38(3), 293-296, 201903
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  17. A Case Report of a Japanese Boy with Morquio A Syndrome: Effects of Enzyme Replacement Therapy Initiated at the Age of 24 Months, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 21(3), 202002
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  18. Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia, HEMATOLOGY REPORTS, 12(1), 2020
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  19. Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations, INTERNATIONAL IMMUNOLOGY, 32(10), 663-671, 202010
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  20. Possible involvement of regulatory T cell abnormalities and variational usage of TCR repertoire in children with autoimmune neutropenia, CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 204(1), 1-13, 202104
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  21. T2-FLAIR Mismatch Sign and Response to Radiotherapy in Diffuse Intrinsic Pontine Glioma, PEDIATRIC NEUROSURGERY, 56(1), 1-9, 202103
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  22. Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings, JOURNAL OF CLINICAL IMMUNOLOGY, 41(5), 975-986, 202107
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