論　文　（原著）　1995年〜1992年

番号 著　　　者　　　名
（共著者も記入）		 論　　文　　題　　名 発表誌名 巻 初頁〜終頁 発行年
31 Tatsumi N, Inui K, Sakai N, Fukushima H, Nishimoto J, Yanagihara I, Nishigaki T, Tsukamoto H, Fu L, Taniike M, Okada S Molecular defects in Krabbe disease Hum Mol Genet 4 1865-1868 1995
32 Kaido M, Fujimura H, Taniike M, Yoshikawa H,Toyooka K, Yorifuji S, Inui K,Okada S, Sparaco M, Yanagihara T Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondria encephalomyopathy (tRNAIle4296 mutation): histochemical, immunohistochemial, and ultrastructual study. J Neurol Sci 131 170-176 1995
33 上松あゆ美、山中　康成、宮崎　文、平松　英文、奥村　光祥、吉田　晃、田中　里江子、百井亨、乾　幸治、岡田　伸太郎 成人型RDS を発症した重症型Hunter症候群（酸性ムコ多糖症TypeIIA ）の一例 日本赤十字社和歌山医療センター医学雑誌 13 91-96 1995
34 Sakai N, Inui K, Midorikawa M, Okuno Y, Ueda S, Iwamatsu A, Okada S Purification and characterization of galactocerebrosidase from human lymphocytes. J Biochem 116 615-620 1994
35 Hayashi J, Ohta S, Kagawa Y, Takai D, Miyabayashi S, Tada K, Fukushima H, Inui K, Okada S, Goto Y, Nonaka I Functional and morphological abnormalities of mitochondria in human cells containing mitochondriaｌDNA with pathogenic point mutations in tRNA genes. J Biol Chem 269 19060-19066 1994
36 Tsukamoto H, Inui K, Matsuoka T, Yanagihara I, Fukushima H, Okada S One base deletion in the cysteine-rich domain of the dysphin gene in Duchenne muscular dystrophy patients. Hum Mol Genet 3 995-996 1994
37 Sakai N, Inui K, Fujii N, Fukushima H, Nishimoto J, Yanagihara I, Isegawa Y, Iwamatsu A, Okada S Krabbe disease: Isolation and characterization of a full-length cDNA for human galactocerebrosidase. Biochem Biophys Res Commun 198 485-491 1994
38 Wada Y, Gu J, Okamoto N, Inui K Diagnosis of carbohydrate -deficient glycoprotein syndrome by matrix-assisted laser desorption time-of-flight mass spectrometery. Biol Mass Spectro 23 108-109 1994
39 Ono J, Kodaka R, Imai K, Itagaki Y, Tanaka J, Inui K, Nagai T, Sakurai K, Harada K, Okada S Evaluation of myelination by means of the T2 value on magnetic resonance imaging. Brain Dev 15 433-438 1993
40 Toyooka K, Fujimura H, Yoshikawa H, Taniike M, Inui K, Yorifuji S, Tarui S, Okada S, Yanagihara T Nephrosialidosis:　ultrastructural and lectin histochemical study. Acta Neuropathol 86 198-205 1993
41 Tsukamoto H, Inui K, Taniike M, Kamiyama K, Hori M, Sumi K, Okada S Different clinical features in monozygotic twins: a case of 7q-syndrome. Clin Genet 43 139-142 1993
42 Tsukamoto H, Sakai N, Taniike M, Nakatsukasa M, Yoshiwara W, Sakamoto H, Fujimura H, Inui K, Okada S Case of ring chromosome 7 : the first report of neuropathological findings.　 Am J Med Genet 46 632-635 1993
43 山下　真理子、山崎　正博、日下　博文、今井　輝国、乾　幸治 発症年齢と臨床型に著しい違いを呈したＧM1 gangliosidosis type３の姉弟例 臨床神経学 33 631-636 1993
44 村松　敬久、土居　義典、米澤　嘉啓、近森　大志郎、山田　光俊、瀬尾　宏美、山崎　文靖、古野　貴志、矢部　敏和、小澤　利男、乾　幸治　 大動脈弁および僧帽弁に高度な肥厚を示したムコ多糖症（Scheie症候群）の１例 J Cardiology 23 183-190 1993
45 Tada K, Taniike M, Ono J, Tsukamoto H, Inui K, Okada S. Serial magnetic resonance imaging studies in a case of late onset globoid cell leukodystrophy. Neuropediatr 23 306-309 1992
46 Wada Y, Nishikawa A, Okamoto N,　Inui K, Tsukamoto H, Okada S, Taniguchi N. Structure of serum transferrin in carbohydrate-deficient　glycoprotein syndrome. Biochem Biophys Res Commun 189 832-836 1992
47 Tsukamoto H, Inui K, Taniike M, Nishimoto J, Midorikawa M, Yoshimine T, Kato A, Ikeda T, Hayakawa T, Okada S. A case of Hallervorden-Spatz disease: progressive and intractable dystonia controlled by bilateral thalamotomy. Brain Dev 14 269-272 1992
48 Taniike M, Fukushima H,　Yanagihara I, Tsukamoto H, Tanaka J, Fujimura H, Nagai T, Sano T, Yamaoka K, Inui K, Okada S.v Mitochondrial tRNAIle　mutation in fatal cardiomyopathy.　 Biochem Biophys Res Commun 186 47-53 1992
49 Inui K, Tsukamoto H, Fukushima H, Taniike M, Tanaka J, Nishigaki T, Okada S. Detection of the A to G (3243) mutation of mitochondrial DNA in Japanes families with mitochondrial encephalomyopathies. J Inher Metab Dis 15 311-314 1992
50 Inui K, Fukushima H, Tsukamoto H, Taniike M, Midorikawa M, Tanaka J, Nishigaki T, Okada S. Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA Leu(UUR) gene. J Pediatr 120 62-66 1992
51 Taniike M, Fujimura H, Kogaki S, Tsukamoto H, Inui K, Midorikawa M, Nishimoto J, Okada S A case of pigmentary type of orthochromatic leukodystrophy with early onset. Acta Neuropathol 83 427-433 1992
52 Yoshida K, Oshima A, Sakuraba H, Nakano T, Yanagisawa N, Inui K, Okada S, Uyama E, Namba R, Kondo K, Iwasaki S, Takamiya K, Suzuki Y. GM1 gangliosidosis in adults: clinical and molecular analysis of 16 Japanese patients. Ann Neurol 31 328-332 1992
53 田中　敏章、日比　逸郎、加藤　精彦、斎藤　史郎、清水　直容、諏訪　成三、　新美　仁男 TAP-144-SR　CPP臨床研究会員（岡田　伸太郎, 乾　幸治, 塚本　浩子） 中枢性思春期早発症におけるsuper long-acting LH-RH アナログ（TAP-144-SR）による６ヵ月間の治療成績 ホルモンと臨床 40 943-949 1992