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3. Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations. (30th June 2020)

4. Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia. Issue 12 (24th May 2017)

6. Description of longitudinal tumor evolution in a case of multiply relapsed clear cell sarcoma of the kidney. Issue 2 (29th December 2021)

8. Effect of kinematics on the torque/force generation, surface characteristics, and shaping ability of a nickel‐titanium rotary glide path instrument: An ex vivo study. (18th March 2022)

10. High ENT1 and DCK gene expression levels are a potential biomarker to predict favorable response to nelarabine therapy in T‐cell acute lymphoblastic leukemia. Issue 4 (2nd August 2019)