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Journal of Clinical Immunology|April 22, 2015
Somatic mosaicism for a NRAS mutation associates with disparate clinical features in RAS-associated leukoproliferative disease: a report of two casesMitsutaka Shiota, Xi Yang, Mei Kubokawa, et al.
Pediatric Blood & Cancer|December 5, 2013
Reduced intensity conditioning in allogeneic stem cell transplantation for AML with Down syndromeHideki Muramatsu, Hirotoshi Sakaguchi, Takashi Taga, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|December 3, 2019
Clinical Outcomes after Allogeneic Hematopoietic Stem Cell Transplantation in Children with Juvenile Myelomonocytic Leukemia: A Report from the Japan Society for Hematopoietic Cell TransplantationNao Yoshida, Hirotoshi Sakaguchi, Miharu Yabe, et al.
Haematologica|May 13, 2014
Peripheral blood lymphocyte telomere length as a predictor of response to immunosuppressive therapy in childhood aplastic anemiaHirotoshi Sakaguchi, Nobuhiro Nishio, Asahito Hama, et al.
Plos One|January 1, 2016
Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic LeukemiaHirotoshi Sakaguchi, Hideki Muramatsu, Yusuke Okuno, et al.
Molecular Genetics and Metabolism Reports|December 7, 2018
Allogeneic stem cell transplantation with reduced intensity conditioning for patients with adrenoleukodystrophyKoji Kato, Ryo Maemura, Manabu Wakamatsu, et al.
American Journal of Hematology|September 10, 2022
Adenovirus disease after hematopoietic cell transplantation: A Japanese transplant registry analysisYoshihiro Inamoto, Wataru Takeda, Tsuneaki Hirakawa, et al.
Haematologica|July 10, 2012
Spliceosomal gene mutations are frequent events in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemiaSarah Abu Kar, Anna Jankowska, Hideki Makishima, et al.
British Journal of Haematology|February 18, 2026
Utility of transplant conditioning intensity score in allogeneic haematopoietic stem cell transplantation for genetic disordersKoji Kawaguchi, Satoshi Miyamoto, Nao Yoshida, et al.
Nature Genetics|July 9, 2013
Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemiaHirotoshi Sakaguchi, Yusuke Okuno, Hideki Muramatsu, et al.
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