栗木 武男 | Pharma Research Laboratories, Hoechst Japan Limited
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概要
関連著者
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栗木 武男
Pharma Research Laboratories, Hoechst Japan Limited
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栗木 武男
Pharma Research And Development Division Hoechst Japan Limited
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栗木 武男
ヘキストジャパン(株)
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佐野 昭光
Pharma Research & Development Division Hoechst Japan Ltd.
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栗木 武男
Laboratory For Chemistry Hoechst Japan Limited
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川島 嘉明
Gifu Pharmaceutical University
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竹内 洋文
Gifu Pharmaceutical University
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丹羽 敏幸
岐阜薬科大学製剤学教室
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丹羽 敏幸
Gifu Pharmaceutical University
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日野 知証
Gifu Pharmaceutical University
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鈴木 恵美
Laboratory For Chemistry Hoechst Japan Limited
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力石 祐次
Hoechst Japan, Ltd., Pharma Research and Development Division, Development Laboratories
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植田 泰誠
Faculty of Pharmaceutical Sciences, Nagoya City University
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力石 祐次
Hoechst Japan Ltd. Pharma Research And Development Division Development Laboratories
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榊原 仁作
名市大院薬
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榊原 仁作
Faculty Of Pharmaceutical Sciences Science University Of Tokyo
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栗木 武男
星薬科大学薬品分析化学教室
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榊原 仁作
Nagoya City Univ. Nagoya Jpn
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浅野 正久
Department of Pharmacology, Nagoya City University Medical School
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力石 祐次
Pharma Research & Development Division, Hoechst Japan Ltd.,
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杉岡 龍夫
Pharma Research Laboratories, Hoechst Japan Limited
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浅野 俊一
Pharma Research Laboratories, Hoechst Japan Limited
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鈴木 恵美
Pharma Research Laboratories, Hoechst Japan Limited
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城塚 美喜雄
Laboratory Shirakawa Site, Nippon Roussel K.K.
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斉藤 健二
Laboratory Shirakawa Site, Nippon Roussel K.K.
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斉藤 健二
Laboratory Shirakawa Site Nippon Roussel K.k.
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浅野 正久
Department Of Pharmacology Nagoya City University Medical School
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今枝 一男
Hoshi College of Pharmacy
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大沢 敬子
Hoshi College of Pharmacy
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大崎 勉
Pharma Research And Development Division Hoechst Japan Limited
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植田 泰誠
Faculty Of Pharmaceutical Sciences Nagoya City University
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榊原 仁作
Faculty Of Pharmaceutical Sciences Nagoya City University
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杉岡 龍夫
Pharma Research Laboratories Hoechst Japan Limited
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Chikaraishi Y
Nippon Hoechst Marion Roussel Ltd. Research And Development Division Preclinical Development Laborat
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浅野 俊一
Pharma Research Laboratories Hoechst Japan Limited
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城塚 美喜雄
Laboratory Shirakawa Site Nippon Roussel K.k.
著作論文
- Stability and Degradation Pattern of Cefpirome (HR 810) in Aqueous Solution
- Particle Design of Tolbutamide by the Spherical Crystallization Technique. V. Improvement of Dissolution and Bioavailability of Direct Compressed Tablets Prepared Using Tolbutamide Agglomerated Crystals
- Particle Design for Antidiabetic Drugs by the Spherical Crystallization Technique. IV. Assessment of Compressibility of Agglomerated Tolbutamide Crystals Prepared by Crystallization Technique
- Particle Design of Tolbutamide by the Spherical Crystallization Technique. III. : Micromeritic Properties and Dissolution Rate of Tolbutamide Spherical Agglomerates Prepared by the Quasi-Emulsion Solvent Diffusion Method and the Solvent Chenge Method
- Particle Design of Tolbutamide by the Spherical Cystallization Technique. II. : Factors Causing Polymorphism of Tolbutamide Spherical Agglomerates
- Studies on Oxygen Determination by the Carrier Gas Method. IX. Determination of Oxygen in Thallium and Thallium Compounds
- Synthesis of Imidazo[4,5-c][1,2,6]thiadiazine 2-Oxides from Hydrolytes of Xanthines and Determination of Their Vasodilating Activity