K. Kudo

发表

Gene alterations involving the CRLF2‐JAK pathway and recurrent gene deletions in Down syndrome‐associated acute lymphoblastic leukemia in Japan

Y. Hayashi, R. Kanezaki, T. Toki, 2014, Genes, chromosomes & cancer.

Presence of respiratory syncytial virus genomic sequences in middle ear fluid and its relationship to expression of cytokines and cell adhesion molecules.

J. Patel, K. Togawa, I. Moro, 1993, The Journal of infectious diseases.

Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond–Blackfan anemia

S. Miyano, S. Ogawa, Kenichi Yoshida, 2020, Bone Marrow Transplantation.

Cytokine expression after the topical administration of substance P to human nasal mucosa. The role of substance P in nasal allergy.

K. Togawa, I. Saito, Y. Okamoto, 1993, Journal of immunology.

Epstein-Barr Virus–Negative Granulomatous Disease Due to SAP Deficiency

H. Kanegane, K. Terui, K. Tanita, 2021, Journal of Clinical Immunology.

Hirosaki Med.J. 71:75―78,2020 CASE STUDY

E. Ito, Sumito Sato, Tatsuya Yamamoto, 2020 .

Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen

T. Morio, T. Toki, E. Ito, 2007, Bone Marrow Transplantation.

Low NUDT15 expression levels due to biallelic NUDT15 variants and 6‐mercaptopurine intolerance

Scott A. Brown, Motohiro Kato, N. Kiyokawa, 2022, British journal of haematology.

Comprehensive genetic analyses of relapsed B-cell precursor acute lymphoblastic leukemia in children

R. Kanezaki, T. Toki, E. Ito, 2019 .

An international retrospective study for tolerability of 6-mercaptopurine on NUDT15 bi-allelic variants in children with acute lymphoblastic leukemia

Hsi-Che Liu, Motohiro Kato, A. Yeoh, 2021, Haematologica.

Mechanism of KIT gene regulation by GATA1 lacking the N-terminal domain in Down syndrome–related myeloid disorders

R. Kanezaki, T. Toki, E. Ito, 2022, Scientific Reports.

Zoledronic acid for relapsed Langerhans cell histiocytosis with isolated skull bone lesion

E. Ito, K. Terui, Akie Kobayashi, 2019, Pediatrics international : official journal of the Japan Pediatric Society.

Voriconazole for both successful treatment of disseminated Trichosporon asahii infection and subsequent cord blood transplantation in an infant with acute myelogenous leukemia

E. Ito, K. Terui, S. Sasaki, 2011, Bone Marrow Transplantation.

Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation

S. Ogawa, Y. Shiozawa, Kenichi Yoshida, 2018, Genes, chromosomes & cancer.

Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21

R. Kanezaki, T. Toki, E. Ito, 2020, Pediatric blood & cancer.

Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing

R. Kanezaki, T. Toki, E. Ito, 2020, Genes, chromosomes & cancer.

Salvage therapy with 2-chlorodeoxyadenosine for refractory and relapsed pediatric Langerhans cell histiocytosis: an updated nationwide survey in Japan

K. Sakamoto, A. Morimoto, Y. Shioda, 2021, International Journal of Hematology.

Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan

M. V. van Zelm, H. Kanegane, T. Morio, 2022, Journal of Clinical Immunology.

Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia

S. Miyano, S. Ogawa, Kenichi Yoshida, 2022, EJHaem.

BRAF V600E-positive cells as molecular markers of bone marrow disease in pediatric Langerhans cell histiocytosis

H. Kanegane, R. Kanezaki, T. Toki, 2022, Haematologica.

Genomic sequences of respiratory syncytial virus in otitis media with effusion

I. Saito, P. Ogra, Y. Okamoto, 1991, The Lancet.

[Detection of RS viral sequences in otitis media effusion from children].

K. Togawa, Y. Okamoto, E. Ito, 1991, Nihon Jibiinkoka Gakkai kaiho.

Guillain-Barré syndrome mimicking acute methotrexate-associated encephalopathy in an adolescent patient with lymphoblastic lymphoma.

E. Ito, K. Terui, S. Sasaki, 2010, Journal of pediatric hematology/oncology.

A Rapid Cytologic Double Staining of Epstein-Barr Virus-encoded Small RNA and Cell Surface Markers for Diagnosis of Epstein-Barr Virus-associated Hemophagocytic Lymphohistiocytosis.

E. Ito, Y. Nakazawa, Tomohiko Sato, 2019, Journal of pediatric hematology/oncology.

Two novel variants of MOZ-CBP fusion transcripts in spontaneously remitted infant leukemia with t(1;16;8)(p13;p13;p11), a new variant of t(8;16)(p11;p13)

E. Ito, Tomohiko Sato, K. Terui, 2008, Haematologica.

Optimal timing of liver transplantation for liver cirrhosis caused by sclerosing cholangitis in a patient with Langerhans cell histiocytosis: a case report

Y. Tanami, K. Mizuta, Y. Ihara, 2022, International Journal of Hematology.

Preceding polydipsia/polyuria, ataxia, and dysarthria in an adult with mixed histiocytosis (Erdheim Chester disease/Langerhans cell histiocytosis)

Takashi Miyoshi, S. Imashuku, S. Tamaki, 2022, Annals of Hematology.

Detection of BRAF V600E mutation in radiological Langerhans cell histiocytosis-associated neurodegenerative disease using droplet digital PCR analysis

K. Sakamoto, A. Morimoto, Y. Shioda, 2023, International Journal of Hematology.

Diplotype analysis of NUDT15 variants and 6-mercaptopurine sensitivity in pediatric lymphoid neoplasms

J. Takita, E. Ito, S. Ito, 2018, Leukemia.

CD7-positive acute myelomonocytic leukemia with trisomy 21 as a sole acquired chromosomal abnormality in two adolescents.

E. Ito, Tomohiko Sato, K. Terui, 2011, Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis.

Childhood acute myeloid leukemia with 5q deletion and HNRNPH1-MLLT10 fusion: the first case report

S. Ogawa, J. Takita, Kenichi Yoshida, 2022, Blood Advances.

A comparison of FLAG-Ida and daunorubicin combined with clofarabine in high-risk acute myeloid leukaemia: data from the UK NCRI AML17 Trial

R. Hills, J. Takita, A. Hunter, 2018, Leukemia.

Early-onset Marfan syndrome with a novel missense mutation: A case report.

T. Toki, K. Terui, Toru Takahashi, 2023, Journal of Cardiology Cases.

Spontaneous remission of skull Langerhans cell histiocytosis that had developed by repeated head injury: illustrative case

A. Kurose, Takahiro Morita, Nozomi Fujiwara, 2023, Journal of Neurosurgery: Case Lessons.

Epithelioid inflammatory myofibroblastic sarcoma harboring ROS 1-TFG fusion ; a case report

E. Ito, S. Yagihashi, H. Mizukami, 2016 .