J. Kobayashi

发表

Analysis of clinical presentations of allergic transfusion reactions and febrile non‐haemolytic transfusion reactions in paediatric patients

Tomohiko Nakamura, K. Sakashita, E. Hidaka, 2019, Vox sanguinis.

PCDH17 functions as a common tumor suppressor gene in acute leukemia and its transcriptional downregulation is mediated primarily by aberrant histone acetylation, not DNA methylation

K. Koike, Y. Nakazawa, K. Sakashita, 2019, International Journal of Hematology.

Relationship between allergic sensitisation-associated single-nucleotide polymorphisms and allergic transfusion reactions and febrile non-haemolytic transfusion reactions in paediatric cases.

Y. Nakazawa, K. Matsuda, T. Takeshita, 2021, Blood transfusion = Trasfusione del sangue.

High frequency of STAT3 gene mutations in T‐cell receptor (TCR)γδ‐type T‐cell large granular lymphocytic leukaemia: implications for molecular diagnostics

K. Oshimi, F. Ishida, Hikaru Kobayashi, 2020, British Journal of Haematology.

T-cell large granular lymphocytic (LGL) leukemia consists of CD4+/CD8dim and CD4-/CD8+ LGL populations in association with immune thrombocytopenia, autoimmune neutropenia, and monoclonal B-cell lymphocytosis

T. Itoh, Takayuki Takahashi, Y. Aoyama, 2019, Journal of clinical and experimental hematopathology : JCEH.

Detection of Bacillus cereus as a causative agent of emetic food poisoning by an unconventional culture procedure.

M. Ohta, J. Kobayashi, N. Kubota, 2022, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

Administration of platelet concentrates suspended in bicarbonated Ringer's solution in children who had platelet transfusion reactions

S. Shimodaira, K. Sakashita, E. Hidaka, 2018, Vox sanguinis.

Early Phase Increase in Serum TIMP-1 in Patients with Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion

J. Kobayashi, N. Kubota, M. Motobayashi, 2022, Children.

Frequent STAT3 mutations in CD8+ T cells from patients with pure red cell aplasia.

M. Hirokawa, K. Matsuda, Toshiro Ito, 2018, Blood advances.

Immature Platelet Fraction and Its Kinetics in Neonates

Y. Nakazawa, F. Ishida, K. Sakashita, 2022, Journal of pediatric hematology/oncology.

T cell clonal expansion and STAT3 mutations: a characteristic feature of acquired chronic T cell-mediated pure red cell aplasia

M. Hirokawa, F. Ishida, S. Nakao, 2022, International Journal of Hematology.

STAT3 mutations in natural killer cells are associated with cytopenia in patients with chronic lymphoproliferative disorder of natural killer cells

F. Ishida, Y. Hirabayashi, N. Sekiguchi, 2019, International Journal of Hematology.

An epidemiologic study of nosocomial infections in a pediatric long-term care facility.

E. Ford-Jones, J. Kobayashi, G. Miller, 1993, American journal of infection control.

Novel Causative RET Mutation in a Japanese Family with Hirschsprung's Disease: Case Report and Factors Impacting Disease Severity

E. Hidaka, T. Hatata, S. Takamizawa, 2020, Journal of Pediatric Genetics.

Reanalysis of Chromosomal Microarray Data Using a Smaller Copy Number Variant Call Threshold Identifies Four Cases with Heterozygous Multiexon Deletions of ARID1B, EHMT1, and FOXP1 Genes

Kyoko Takano, Eriko Nishi, K. Wakui, 2023, Molecular Syndromology.