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Diagnostics (Basel, Switzerland)|October 23, 2021
High-Risk Screening for Fabry Disease: A Nationwide Study in Japan and Literature ReviewTakaaki Sawada, Jun Kido, Keishin Sugawara, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 11, 2021
Possible roles of anti-type II collagen antibody and innate immunity in the development and progression of diabetic retinopathyTsunehiko Ikeda, Kimitoshi Nakamura, Teruyo Kida, et al.
Advances in Experimental Medicine and Biology|July 30, 2017
Tyrosinemia Type I in Japan: A Report of Five CasesKimitoshi Nakamura, Michinori Ito, Yosuke Shigematsu, et al.
World Journal of Hepatology|August 8, 2019
Wilson disease developing osteoarthritic pain in severe acute liver failure: A case reportJun Kido, Shirou Matsumoto, Keishin Sugawara, et al.
Respiratory Medicine Case Reports|July 7, 2018
Liposteroid and methylprednisolone combination therapy for a case of idiopathic lung hemosiderosisRieko Sakamoto, Shiro Matsumoto, Hiroshi Mitsubuchi, et al.
The Journal of Nutrition|May 22, 2007
Animal models of tyrosinemiaKimitoshi Nakamura, Yasuhiko Tanaka, Hiroshi Mitsubuchi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|July 22, 2014
Diagnosis and treatment of urea cycle disorder in JapanKimitoshi Nakamura, Jun Kido, Hiroshi Mitsubuchi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 17, 2014
Biochemical and clinical features of hereditary hyperprolinemiaHiroshi Mitsubuchi, Kimitoshi Nakamura, Shirou Matsumoto, et al.
The Journal of Nutrition|September 23, 2008
Inborn errors of proline metabolismHiroshi Mitsubuchi, Kimitoshi Nakamura, Shiro Matsumoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 3, 2014
Diagnosis and treatment of hereditary tyrosinemia in JapanKimitoshi Nakamura, Shirou Matsumoto, Hiroshi Mitsubuchi, et al.
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