If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where Koji Kato is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 20 Similar Profiles
Hematopoietic Stem Cell Transplantation Medicine & Life Sciences
Fetal Blood Medicine & Life Sciences
Transplantation Medicine & Life Sciences
Graft vs Host Disease Medicine & Life Sciences
Stem Cell Transplantation Medicine & Life Sciences
Japan Medicine & Life Sciences
Precursor Cell Lymphoblastic Leukemia-Lymphoma Medicine & Life Sciences
Transplants Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1985 2019

Allogeneic stem cell transplantation with reduced intensity conditioning for patients with adrenoleukodystrophy

Kato, K., Maemura, R., Wakamatsu, M., Yamamori, A., Hamada, M., Kataoka, S., Narita, A., Miwata, S., Sekiya, Y., Kawashima, N., Suzuki, K., Narita, K., Doisaki, S., Muramatsu, H., Sakaguchi, H., Matsumoto, K., Koike, Y., Onodera, O., Kaga, M., Shimozawa, N. & 1 others, Yoshida, N., Mar 1 2019, In : Molecular Genetics and Metabolism Reports. 18, p. 1-6 6 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Stem Cell Transplantation
Internal Capsule
Transplantation
Fetal Blood
2 Citations (Scopus)

A retrospective analysis of haplo-identical HLA-mismatch hematopoietic transplantation without posttransplantation cyclophosphamide for GVHD prophylaxis in patients with adult T-cell leukemia–lymphoma

on behalf of ATL Working Group of the Japan Society for Hematopoietic Cell Transplantation, Aug 1 2019, In : Bone Marrow Transplantation. 54, 8, p. 1266-1274 9 p.

Research output: Contribution to journalArticle

Cyclophosphamide
Hematopoietic Stem Cell Transplantation
Transplantation
T-Lymphocytes
Tissue Donors

Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (Journal of Human Genetics, (2017), 62, 9, (861-863), 10.1038/jhg.2017.53)

Kato, K., Miya, F., Hori, I., Ieda, D., Ohashi, K., Negishi, Y., Hattori, A., Okamoto, N., Kato, M., Tsunoda, T., Yamasaki, M., Kanemura, Y., Kosaki, K. & Saitoh, S., Jul 1 2019, In : Journal of Human Genetics. 64, 7, p. 701-702 2 p.

Research output: Contribution to journalComment/debate

Open Access
Periventricular Nodular Heterotopia
Medical Genetics
Cleft Palate
Missense Mutation
Mutation

Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex

Kato, K., Oka, Y., Muramatsu, H., Vasilev, F. F., Otomo, T., Oishi, H., Kawano, Y., Kidokoro, H., Nakazawa, Y., Ogi, T., Takahashi, Y. & Saitoh, S., Jan 1 2019, (Accepted/In press) In : Journal of medical genetics.

Research output: Contribution to journalArticle

Genes
Chondrodysplasia Punctata
Coloboma
Microphthalmos
Exome
35 Citations (Scopus)

Brentuximab vedotin with chemotherapy for CD30-positive peripheral T-cell lymphoma (ECHELON-2): a global, double-blind, randomised, phase 3 trial

ECHELON-2 Study Group, Jan 19 2019, In : The Lancet. 393, 10168, p. 229-240 12 p.

Research output: Contribution to journalArticle

Peripheral T-Cell Lymphoma
Drug Therapy
Vincristine
Prednisone
Doxorubicin