ACTN1 Mutations Cause Congenital Macrothrombocytopenia von Kunishima, Shinji, Okuno, Yusuke, Yoshida, Kenichi, Shiraishi, Yuichi, Sanada, Masashi, Muramatsu, Hideki, Chiba, Kenichi, Tanaka, Hiroko, Miyazaki, Koji, Sakai, Michio, Ohtake, Masatoshi, Kobayashi, Ryoji, Iguchi, Akihiro, Niimi, Gen, Otsu, Makoto, Takahashi, Yoshiyuki, Miyano, Satoru, Saito, Hidehiko, Kojima, Seiji, Ogawa, Seishi

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Compound Heterozygous Mutations in the Cholesterol Side-Chain Cleavage Enzyme Gene (CYP11A) Cause Congenital Adrenal Insufficiency in Humans von Katsumata, Noriyuki, Ohtake, Masatoshi, Hojo, Toru, Ogawa, Eishin, Hara, Takayuki, Sato, Naoko, Tanaka, Toshiaki

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Acute encephalopathy with a truncation mutation in the SCN1A gene: A case report von Takayanagi, Masaru, Haginoya, Kazuhiro, Umehara, Naoki, Kitamura, Taro, Numata, Yurika, Wakusawa, Keisuke, Hino‐Fukuyo, Naomi, Mazaki, Emi, Yamakawa, Kazuhiro, Ohura, Toshihiro, Ohtake, Masatoshi

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Acute Encephalopathy Associated With Influenza C Virus Infection von Takayanagi, Masaru, Umehara, Naoki, Watanabe, Hiroshi, Kitamura, Taro, Ohtake, Masatoshi, Nishimura, Hidekazu, Matsuzaki, Yoko, Ichiyama, Takashi

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Compound Heterozygous Mutations in the Cholesterol Side-Chain Cleavage Enzyme Gene (CYP11A) Cause Congenital Adrenal Insufficiency in Humans von Katsumata, Noriyuki, Ohtake, Masatoshi, Hojo, Toru, Ogawa, Eishin, Hara, Takayuki, Sato, Naoko, Tanaka, Toshiaki

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Acute encephalopathy with a truncation mutation in the SCNIA gene: A case report von TAKAYANAGI, Masaru, HAGINOYA, Kazuhiro, OHTAKE, Masatoshi, UMEHARA, Naoki, KITAMURA, Taro, NUMATA, Yurika, WAKUSAWA, Keisuke, HINO-FUKUYO, Naomi, MAZAKI, Emi, YAMAKAWA, Kazuhiro, OHURA, Toshihiro

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A Case of Langerhans Cell Histiocytosis who Died from Liver Cirrhosis von OHTAKE, Masatoshi, MORIYA, Kunihiko, CHIKAOKA, Shuji

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Esophagomediastinal Fistula as a Complication of Tuberculous Mediastinal Lymphadenitis von OHTAKE, Masatoshi, SAITO, Hiroshi, OKUNO, Motoyasu, YAMAMOTO, Shigeyoshi, OHGIMI, Tatsuo

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Changes in zinc and copper concentrations in breast milk and blood of Japanese women during lactation von Ohtake, M. (Tohoku Univ., Sendai (Japan). School of Medicine), Tamura, T

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Essential Thrombocythemia in a Girl Associated with Acquired von Willebrand Disease von OHTAKE, Masatoshi, SUZUKI, Rikio, CHIKAOKA, Shuji

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Serum Zinc and Copper Levels in Healthy Japanese Infants von OHTAKE, MASATOSHI

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Zinc and Copper Concentrations in Human Milk and in Serum from Exclusively-Breast-Fed Infants during the First 3 Months of Life von OHTAKE, MASATOSHI, CHIBA, RYO, MOCHIZUKI, KEIKO, TADA, KEIYA

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Serum Zinc and Copper Levels in Healthy Japanese Children von OHTAKE, MASATOSHI, TAMURA, TSUNENOBU

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Lymphoblasts and Diagnosis of Pyruvate Carboxylase Deficiency von TAKADA, GORO, OHTAKE, MASATOSHI, MIYABAYASHI, SHIGEAKI, TADA, KEIYA

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Chronic Hypernatremia Associated with Holoprosencephaly von OHTAKE, MASATOSHI, SUZUKI, HIROSHI, IGARASHI, YUTAKA, KOBAYASHI, YASUKO, SAITO, TETSU

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Efficacy of Twice‐Daily Cimetidine in Pediatric Peptic Ulcer von Kato, Seiichi, Ozawa, Akira, Shibuya, Hidenori, Ohtake, Masatoshi, Nakagawa, Hiroshi

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Degeneration of Respiratory System in Sea Urchin Spermatozoa during Incubation in Seawater for Long Duration von Tateru Ohtake, Masatoshi Mita, Akiko Fujiwara, Eigoro Tazawa, Ikuo Yasumasu

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Efficacy of Twice-Daily Cimetidine in Pediatric Peptic Ulcer von Kato, Seiichi, Ozawa, Akira, Shibuya, Hidenori, Ohtake, Masatoshi, Nakagawa, Hiroshi

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Modification and Pyroelectricity of Pb(Zr, Ti)O3-Based Ceramics Using HIP with Novel Glass Encapsulation von SUGIYAMA, Osamu, OHTAKE, Masatoshi, KUWAHARA, Hiroshi, OHSUMI, Shuzo, KATO, Kazuaki, FUKUSHIMA, Toshihiro, KANEKO, Shoji

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Information recording method and apparatus with suppressed mark edge jitters von Miyamoto, Makoto, Toda, Tsuyoshi, Ohtake, Masatoshi, Terao, Motoyasu, Ushiyama, Junko, Andoo, Keikichi, Anzai, Yumiko, Hirotsune, Akemi, Nishida, Tetsuya, Saga, Hideki

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