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Molecular Genetics and Metabolism|August 11, 2006
Gene expression profiles of homogentisate-treated Fah-/- Hpd-/-mice using DNA microarraysYasuhiko Tanaka, Kimitoshi Nakamura, Shirou Matsumoto, et al.Clinical Ophthalmology (Auckland, N.Z.)|May 31, 2014
Progression of nuclear sclerosis based on changes in refractive values after lens-sparing vitrectomy in proliferative diabetic retinopathyTsunehiko Ikeda, Masahiro Minami, Kimitoshi Nakamura, et al.Clinical Case Reports|April 29, 2024
Serum brain natriuretic peptide levels may be a useful marker for early diagnosis of cardiomyopathy secondary to neuroblastoma: A case reportNatsumi Fujiyama, Osamu Matsuo, Takahiro Yamashita, et al.Molecular Genetics and Metabolism Reports|June 22, 2026
Newborn screening for Fabry disease in Japan: an additional 3-year reportTakaaki Sawada, Jun Kido, Keishin Sugawara, et al.Experimental and Clinical Transplantation : Official Journal of the Middle East Society for Organ Transplantation|November 23, 2021
Complete Remission of Refractory Immunothrombocytopenic Purpura After Tacrolimus Replacement With Cyclosporine in a Case of Living Related Liver TransplantMasayoshi Hamaguchi, Rieko Sakamoto, Kensaku Kohrogi, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 26, 2022
Muscle biochemical and pathological diagnosis in Pompe diseaseYoshihiko Saito, Kimitoshi Nakamura, Tokiko Fukuda, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|September 11, 2016
Citrulline for urea cycle disorders in JapanKenichi Tanaka, Kimitoshi Nakamura, Shirou Matsumoto, et al.The Journal of Biological Chemistry|October 16, 2002
Cardiac-specific expression of calcineurin reverses embryonic lethality in calreticulin-deficient mouseLei Guo, Kimitoshi Nakamura, Jeffery Lynch, et al.International Journal of Pediatric Otorhinolaryngology|July 7, 2022
Therapeutic outcomes of laryngeal closure and laryngostomy in children with recurrent pneumoniaDaizo Murakami, Satoru Miyamaru, Kohei Nishimoto, et al.Human Genome Variation|June 4, 2026
Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variantHitoshi Kashiki, Jun Kido, Yohei Misumi, et al.Pageof 23