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Journal of Inherited Metabolic Disease|February 15, 2014
Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation [corrected]Yoko Nakajima, Judith Meijer, Doreen Dobritzsch, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 20, 2018
Biallelic GALM pathogenic variants cause a novel type of galactosemiaYoichi Wada, Atsuo Kikuchi, Natsuko Arai-Ichinoi, et al.
BMC Gastroenterology|November 16, 2019
Three cases of histologically proven hepatic epithelioid hemangioendothelioma evaluated using a second-generation microbubble contrast medium in ultrasonography: case reportsJun Arai, Yuu Shimozuma, Yumi Otoyama, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2020
Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemiaYoichi Wada, Atsuo Kikuchi, Natsuko Arai-Ichinoi, et al.
In Vivo (Athens, Greece)|July 2, 2020
Laparoscopic Treatment of a Hepatoduodenal Ligament Schwannoma With Infrared Indocyanine Green FluorescenceKodai Tomioka, Takeshi Aoki, Tomotake Koizumi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2024
Phenotypic and genetic spectra of galactose mutarotase deficiency: A nationwide survey conducted in JapanYasuko Mikami-Saito, Yoichi Wada, Natsuko Arai-Ichinoi, et al.
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