K. Imagawa

发表

A novel BBS10 mutation identified in a patient with Bardet–Biedl syndrome with a violent emotional outbreak

K. Kosaki, T. Takenouchi, Tomoko Uehara, 2017, Human Genome Variation.

Interinstitutional patient transfers between rapid chemotherapy cycles were feasible to utilize proton beam therapy for pediatric Ewing sarcoma family of tumors.

H. Sakurai, S. Sakashita, T. Masumoto, 2018, Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology.

Prediction of interindividual differences in hepatic functions and drug sensitivity by using human iPS-derived hepatocytes

K. Harada, H. Mizuguchi, E. Noguchi, 2014, Proceedings of the National Academy of Sciences.

Time course of peripheral immunophenotypes of multisystem inflammatory syndrome in children

H. Takada, S. Hosaka, A. Morita, 2022, Clinical Immunology.

Vaccination for Patients with Inborn Errors of Immunity: a Nationwide Survey in Japan

T. Morio, H. Takada, S. Nonoyama, 2021, Journal of Clinical Immunology.

Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis

S. Ito, Shinji Saitoh, Tokio Sugiura, 2022, JPGN reports.

An Adult Patient with Alagille Syndrome Showing Mainly Renal Failure and Vascular Abnormality without Liver Manifestation

Masaki Kobayashi, K. Hirayama, H. Shimohata, 2020, Internal medicine.

22q11.2 Duplication Syndrome with Persistent 5th Aortic Arch

H. Horigome, Y. Hiramatsu, N. Ishikawa, 2019, Pediatric Cardiology and Cardiac Surgery.

Genotyping NUDT15 can predict the dose reduction of 6-MP for children with acute lymphoblastic leukemia especially at a preschool age

N. Kiyokawa, E. Noguchi, Hisato Suzuki, 2016, Journal of Human Genetics.

Generation of a bile salt export pump deficiency model using patient-specific induced pluripotent stem cell-derived hepatocyte-like cells

K. Harada, H. Mizuguchi, E. Noguchi, 2017, Scientific Reports.

Case report: Immunological characteristics of de novo ulcerative colitis in a child post COVID-19

H. Takada, M. Tagawa, Noriaki Sakamoto, 2023, Frontiers in Immunology.

Preaxial polydactyly in an individual with Wiedemann‐Steiner syndrome caused by a novel nonsense mutation in KMT2A

K. Kosaki, T. Takenouchi, Tomoko Uehara, 2017, American journal of medical genetics. Part A.

Genome analysis in sick neonates and infants: high-yield phenotypes and contribution of small copy number variations.

Masatoshi Kondo, R. Kosaki, K. Kosaki, 2022, The Journal of pediatrics.

Vaccination for Patients with Inborn Errors of Immunity: a Nationwide Survey in Japan

T. Morio, H. Takada, S. Nonoyama, 2021, Journal of Clinical Immunology.

Kawasaki disease with dilatation of the common bile duct: A case report and review of literature

H. Takada, M. Tagawa, A. Morita, 2021, International journal of rheumatic diseases.

Clinical phenotype and molecular analysis of a homozygous ABCB11 mutation responsible for progressive infantile cholestasis

H. Kusuhara, M. Kage, K. Tanikawa, 2018, Journal of Human Genetics.

Proposal of a liver histology‐based scoring system for bile salt export pump deficiency

Y. Zen, H. Kondou, M. Kage, 2020, Hepatology research : the official journal of the Japan Society of Hepatology.

Variants in KIF2A cause broad clinical presentation; the computational structural analysis of a novel variant in a patient with a cortical dysplasia, complex, with other brain malformations 3

H. Takada, K. Kosaki, T. Takenouchi, 2021, American journal of medical genetics. Part A.

Human ESC/iPSC-Derived Hepatocyte-like Cells Achieve Zone-Specific Hepatic Properties by Modulation of WNT Signaling.

H. Mizuguchi, F. Sakurai, M. Tachibana, 2017, Molecular therapy : the journal of the American Society of Gene Therapy.

Immunological characteristics of severe acute hepatitis of unknown origin in a child post SARS-CoV-2 infection

K. Asayama, H. Takada, D. Matsubara, 2022, Clinical Immunology.

Initial manifestations in Patients with Inborn Errors of Immunity Based on Onset Age: a Study from a Nationwide Survey in Japan

T. Morio, H. Takada, S. Nonoyama, 2023, Journal of Clinical Immunology.

A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2

H. Takada, T. Takenouchi, Tomoko Uehara, 2019, Clinical case reports.

A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay

H. Takada, K. Kosaki, T. Takenouchi, 2019, Human genome variation.

Pneumococcal Serotype-specific Opsonophagocytic Activity in Interleukin-1 Receptor-associated Kinase 4-deficient Patients.

H. Takada, S. Okada, S. Nishimura, 2021, The Pediatric infectious disease journal.

Transient myelodysplasia triggered by parvovirus B19 infection in a male with inborn error of bile acid metabolism

H. Nittono, Y. Yuza, A. Inui, 2023, Pediatric blood & cancer.

Infliximab for the Treatment of Refractory Kawasaki Disease: A Nationwide Survey in Japan

I. Takeuchi, T. Shiraishi, Tomio Kobayashi, 2017, The Journal of pediatrics.

A Case of Anorexia Nervosa with Focal Cortical Dysplasia

H. Takada, T. Enokizono, T. Ohto, 2024, Case reports in psychiatry.

Schuurs‐Hoeijmakers syndrome in two patients from Japan

K. Kosaki, T. Takenouchi, Tomoko Uehara, 2018, American journal of medical genetics. Part A.

Abdominal aortic thrombus formation in a neonate with an interrupted aortic arch

H. Takada, H. Horigome, H. Kato, 2021, Clinical case reports.