Hematology/Oncology/Cardiovascular

Fingerprint The fingerprint is based on mining the text of the scientific documents related to the associated persons. Based on that an index of weighted terms is created, which defines the key subjects of research unit

Hematopoietic Stem Cell Transplantation Medicine & Life Sciences
Peripheral Blood Stem Cell Transplantation Medicine & Life Sciences
Drug Therapy Medicine & Life Sciences
Transplantation Medicine & Life Sciences
Acute Myeloid Leukemia Medicine & Life Sciences
Granulocyte Colony-Stimulating Factor Medicine & Life Sciences
Therapeutics Medicine & Life Sciences
Stem Cell Transplantation Medicine & Life Sciences

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Research Output 1991 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 othersYoshida, 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

Anemia in Patients with Severe Aortic Stenosis

CURRENT AS Registry Investigators, Dec 1 2019, In : Scientific reports. 9, 1, 1924.

Research output: Contribution to journalArticle

Open Access
Aortic Valve Stenosis
Anemia
Confidence Intervals
Aortic Valve
Hemoglobins

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., Jan 1 2019, In : Journal of Human Genetics.

Research output: Contribution to journalComment/debate

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