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Journal of Human Genetics|December 6, 2018
Carnitine palmitoyltransferase II deficiency with a focus on newborn screeningGo Tajima, Keiichi Hara, Miori Yuasa
Chemistry, an Asian Journal|May 9, 2008
Catalytic asymmetric epoxidation of alpha,beta-unsaturated phosphane oxides with a Y(O-iPr)3/biphenyldiol complexKeiichi Hara, So-Young Park, Noriyuki Yamagiwa, et al.
Pediatric Hematology and Oncology|July 7, 2009
Successful treatment of Kasabach-Merritt syndrome with vincristine and diagnosis of the hemangioma using three-dimensional imagingKeiichi Hara, Tomoaki Yoshida, Teruyuki Kajiume, et al.
Indian Journal of Pediatrics|September 2, 2016
Primary Carnitine Deficiency - A Rare Treatable Cause of Cardiomyopathy and Massive HepatomegalyShivani Deswal, Sunita Bijarnia-Mahay, Vinamr Manocha, et al.
Molecular Genetics and Metabolism|November 19, 2016
Screening of MCAD deficiency in Japan: 16years' experience of enzymatic and genetic evaluationGo Tajima, Keiichi Hara, Miyuki Tsumura, et al.
Journal of the American Chemical Society|September 7, 2006
Mixed La-Li heterobimetallic complexes for tertiary nitroaldol resolutionShin-ya Tosaki, Keiichi Hara, Vijay Gnanadesikan, et al.
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