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[文献書誌] Suzuki Y, Tsukuda K, Taniyama M, Atsumi Y, Matsuoka K, Oka Y: "Lipoma and sensory neuropathy in mitochondrial diabetes associated with tRNA mutation at position 3271"Diabetes Care. 25. 407-408 (2002)
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[文献書誌] Tanizawa Y, Nakai K, Sasaki T, Anno T, Ohta Y, Inoue H, Matuo K, Koga M, Furukawa S, Oka Y: "Unregulated elevation of glutamate dehydrogenase activity induces glutamine-stimulated insulin secretion : Identification and characterization of a GLUD1 gene mutation, and insulin secretion studies with MIN6 cells overexpressing the mutant GDH"Diabetes. 51. 712-717 (2002)
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[文献書誌] Yamasoba T, Goto Yu-ichi, Oka Y, Nishino I, Tsukuda K, Nonaka I: "Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to G point mutation in the mitochondrial ribosomal RNA gene"Neuromuscular Disorders. 12. 506-512 (2002)
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[文献書誌] Suzuki Y, Suzuki S, Taniyama M, Muramatsu T, Ohta S, Oka Y, Atsumi Y, Matsuoka K: "Multiple cranial mononeuropathies with acetylcholine receptor antibody in mitochondrial diabetes"Diabetes Care. (in press). (2002)
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[文献書誌] Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, Smith RJ, Timmermans J-P, Van Camp G: "The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells"Histochemistry and Cell Biology. (in press). (2003)
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[文献書誌] Wenyi Z, Suzuki S, Hirai H, Hinokio Y, Tanizawa Y, Matsutani M, Satoh J, Oka Y: "Role of Urotensin II Gene in the Genetic Susceptibility to Type 2 Diabetes Mellitus in Japanese"Diabetologia. (in press). (2003)
