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Molecular Genetics and Metabolism Reports|October 4, 2017
Elosulfase alfa enzyme replacement therapy attenuates disease progression in a non-ambulatory Japanese patient with Morquio A syndrome (case report)Misako Hiramatsu, Kimitoshi NakamuraPathogens (Basel, Switzerland)|October 23, 2021
Oral Immunotherapy for Children with Cow's Milk AllergyMika Ogata, Jun Kido, Kimitoshi NakamuraCase Reports in Pediatrics|April 2, 2020
Carglumic Acid Contributes to a Favorable Clinical Course in a Case of Severe Propionic AcidemiaJun Kido, Shirou Matsumoto, Kimitoshi NakamuraAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 12, 2011
Newborn screening for lysosomal storage disordersKimitoshi Nakamura, Kiyoko Hattori, Fumio EndoMolecular and Cellular Neurosciences|August 24, 2020
Role of induced pluripotent stem cells in lysosomal storage diseasesJun Kido, Kimitoshi Nakamura, Takumi EraPediatrics International : Official Journal of the Japan Pediatric Society|November 3, 2011
Effect of body mass index-z score on adverse levels of cardiovascular disease risk factorsKeisuke Katsuren, Kimitoshi Nakamura, Takao OhtaCardiology in the Young|June 3, 2022
Torsion of wandering spleen after Fontan operation in a patient with situs inversus: a rare complicationFumiya Miyamura, Osamu Matsuo, Kimitoshi NakamuraInternational Journal of Neonatal Screening|October 19, 2020
Newborn Screening for Pompe DiseaseTakaaki Sawada, Jun Kido, Kimitoshi NakamuraFrontiers in Genetics|January 30, 2023
Gene therapy for lysosomal storage diseases: Current clinical trial prospectsJun Kido, Keishin Sugawara, Kimitoshi NakamuraJournal of Inherited Metabolic Disease|March 1, 2018
Mulberries in the urine: a tell-tale sign of Fabry diseasePin Fee Chong, Kimitoshi Nakamura, Ryutaro KiraPageof 23