REYE'S SYNDROME: SERUM GLUTAMIC OXALACETIC TRANSAMINASE ISOZYMES AND ORNITHINE TRANSCARBAMYLASE ACTIVITY
スポンサーリンク
概要
著者
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YOSHINO Makoto
Department of Pediatrics and Child Health, Kurume University School of Medicine
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Yoshino Makoto
Department Of Advanced Materials Science & Engineering Faculty Of Engineering Yamaguchi Universi
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YAMASHITA FUMIO
Department of Child Health, Kurume University School of Medicine
関連論文
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- 遅発型オルニチントランスカルバミラーゼ欠損症男性患者における予後因子と血漿アミノ酸プロフィールの特徴
- Synthesis and Gas Permeation Properties of Star-like Poly(ethylene oxide)s Using Hyperbranched Polyimide as Central Core
- Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency
- Pyruvate dehydrogenase E1α subunit deficiency in a female patient : evidence of antenatal origin of brain damage and possible etiology of infantile spasms
- Investigation of the IVS5 +5G → A splice site mutation of HPS1 gene found in Japanese patients with Hermansky-Pudlak syndrome
- Carotenoids Formation by a Facultative Methylotroph, Protaminobacter ruber
- 日本における新生児スクリーニング使用済み濾紙血の目的外使用と長期保存
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- A long-term survival case of arginase deficiency with severe multicystic white matter and compound mutations
- Pyruvate dehydrogenase E1 alpha subunit deficiency in a female patient: evidence of antenatal origin of brain damage and possible etiology of infantile spasms
- Effects of Image Distortion Correction on Voxel-based Morphometry
- Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations
- Mucolipidosis II and III alpha/beta : mutation analysis of 40 Japanese patients showed genotype-phenotype correlation
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- EVALUATION OF ALTERNTAE-DAY STEROID THERAPY FOR NEPHROTIC SYNDROME IN CHILDHOOD BY CROSS-OVER STUDY
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- International Comparative Study of Childhood Malignancy Comparative Study of Pediatric Malignancy between Kurume and Karachi (K-K Project 1991).
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- DIAGNOSIS OF REYE SYNDROME
- Arginase activity in peripheral erythrocytes in developing individuals.
- REYE'S SYNDROME: SERUM GLUTAMIC OXALACETIC TRANSAMINASE ISOZYMES AND ORNITHINE TRANSCARBAMYLASE ACTIVITY
- A case of hemolytic anemia in Wilson's disease no evidence for abnormal erythrocyte enzyme activities.