Mutation spectrum of α-Galactosidase gene in Japanese patients with Fabry disease von Kobayashi, Masahisa, Ohashi, Toya, Kaneshiro, Eiko, Higuchi, Takashi, Ida, Hiroyuki

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Role of Longitudinal Strain in the Evaluation of Contractile Dysfunction in Japanese Fabry Disease Patients von Nojiri, Ayumi, Morimoto, Satoshi, Fukuro, Eiko, Okuyama, Toraaki, Anan, Ikuko, Kawai, Makoto, Sakurai, Ken, Kobayashi, Masahisa, Kobayashi, Hiroshi, Ida, Hiroyuki, Ohashi, Toya, Yoshimura, Michihiro, Eto, Yoshikatsu, Hongo, Kenichi

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Clinical findings of gadolinium-enhanced cardiac magnetic resonance in Fabry patients von Nojiri, Ayumi, Anan, Ikuko, Morimoto, Satoshi, Kawai, Makoto, Sakuma, Toru, Kobayashi, Masahisa, Kobayashi, Hiroshi, Ida, Hiroyuki, Ohashi, Toya, Eto, Yoshikatsu, Shibata, Takahiro, Yoshimura, Michihiro, Hongo, Kenichi

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The beneficial effects of long-term enzyme replacement therapy on cardiac involvement in Japanese Fabry patients von Hongo, Kenichi, Ito, Keiichi, Date, Taro, Anan, Ikuko, Inoue, Yasunori, Morimoto, Satoshi, Ogawa, Kazuo, Kawai, Makoto, Kobayashi, Hiroshi, Kobayashi, Masahisa, Ida, Hiroyuki, Ohashi, Toya, Taniguchi, Ikuo, Yoshimura, Michihiro, Eto, Yoshikatsu

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Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST) von Saito, Osamu, Kusano, Eiji, Akimoto, Tetsu, Asano, Yasushi, Kitagawa, Teruo, Suzuki, Ken, Ishige, Nobuyuki, Akiba, Takashi, Saito, Akira, Ishimura, Eiji, Hattori, Motoshi, Hishida, Akira, Guili, Chu, Maruyama, Hiroki, Kobayashi, Masahisa, Ohashi, Touya, Matsuda, Ichiro, Eto, Yoshikatsu

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Experience with enteral sulfonylurea monotherapy for extremely low birth weight infants with hyperglycemia von Nakagawa, Ai, Hirano, Daishi, Inage, Yuka, Yamada, Saya, Kotake, Yuko, Ikoma, Naohiro, Kumazawa, Kensuke, Hayashi, Shion, Tanabe, Yukitoshi, Kobayashi, Masahisa, Shimizu, Masaki

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Massive accumulation of globotriaosylceramide in various tissues from a Fabry patient with a high antibody titer against alpha-galactosidase A after 6 years of enzyme replacement t... von Hongo, Kenichi, Harada, Toru, Fukuro, Eiko, Kobayashi, Masahisa, Ohashi, Toya, Eto, Yoshikatsu

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Rapid Immunochromatographic Detection of Serum Anti-α-Galactosidase A Antibodies in Fabry Patients after Enzyme Replacement Therapy von Nakano, Sachie, Tsukimura, Takahiro, Togawa, Tadayasu, Ohashi, Toya, Kobayashi, Masahisa, Takayama, Katsuyoshi, Kobayashi, Yukuharu, Abiko, Hiroshi, Satou, Masatsugu, Nakahata, Tohru, Warnock, David G, Sakuraba, Hitoshi, Shibasaki, Futoshi

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The role of native T1 values on the evaluation of cardiac manifestation in Japanese Fabry disease patients von Anan, Ikuko, Sakuma, Toru, Fukuro, Eiko, Morimoto, Satoshi, Nojiri, Ayumi, Kawai, Makoto, Sakurai, Ken, Kobayashi, Masahisa, Kobayashi, Hiroshi, Ida, Hiroyuki, Ohashi, Toya, Yoshimura, Michihiro, Eto, Yoshikatsu, Hongo, Kenichi

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Risk factors for hyperglycemia in extremely low birth weight infants during the first 14 days von Inage, Yuka, Hirano, Daishi, Nakagawa, Ai, Yamada, Saya, Kotake, Yuko, Ikoma, Naohiro, Kumazawa, Kensuke, Hayashi, Shion, Tanabe, Yukitoshi, Kobayashi, Masahisa, Shimizu, Masaki

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Characteristics of the Electrocardiogram in Japanese Fabry Patients Under Long-Term Enzyme Replacement Therapy von Morimoto, Satoshi, Nojiri, Ayumi, Fukuro, Eiko, Anan, Ikuko, Kawai, Makoto, Sakurai, Ken, Kobayashi, Masahisa, Kobayashi, Hiroshi, Ida, Hiroyuki, Ohashi, Toya, Shibata, Takahiro, Yoshimura, Michihiro, Eto, Yoshikatsu, Hongo, Kenichi

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Characteristics of Cerebral Microbleeds in Patients with Fabry Disease von Kono, Yu, MD, PhD, Wakabayashi, Taichi, MD, Kobayashi, Masahisa, MD, PhD, Ohashi, Toya, MD, PhD, Eto, Yoshikatsu, MD, PhD, Ida, Hiroyuki, MD, PhD, Iguchi, Yasuyuki, MD, PhD

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Novel TFAP2A mutation in a Japanese family with Branchio-oculo-facial syndrome von Sato, Taisuke, Samura, Osamu, Kato, Noriko, Taniguchi, Kosuke, Takahashi, Ken, Ito, Yuki, Aoki, Hiroaki, Kobayashi, Masahisa, Migita, Ohsuke, Okamoto, Aikou, Hata, Kenichiro

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Biallelic mutations of EGFR in a compound heterozygous state cause ectodermal dysplasia with severe skin defects and gastrointestinal dysfunction von Hayashi, Shion, Yokoi, Takayuki, Hatano, Chihiro, Enomoto, Yumi, Tsurusaki, Yoshinori, Naruto, Takuya, Kobayashi, Masahisa, Ida, Hiroyuki, Kurosawa, Kenji

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A first fatal neonatal case of Enterobacter sakazakii infection in Japan von Teramoto, Satoshi, Tanabe, Yukitoshi, Okano, Erika, Nagashima, Tatsuo, Kobayashi, Masahisa, Etoh, Yoshikatsu

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Significance of screening for Fabry disease among male dialysis patients von Ichinose, Mayuri, Nakayama, Masaaki, Ohashi, Toya, Utsunomiya, Yasunori, Kobayashi, Masahisa, Eto, Yoshikatsu

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Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally von Okamoto, Aikou, Kobayashi, Masahisa, Aoki, Hiroaki, Kajiwara, Kazuhiro, Ito, Yuki, Matsuoka, Tomona, Sato, Taisuke, Samura, Osamu, Hasegawa, Akihiro, Inage, Yuka

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Non-invasive screening method for Fabry disease by measuring globotriaosylceramide in whole urine samples using tandem mass spectrometry von Kitagawa, Teruo, Ishige, Nobuyuki, Suzuki, Ken, Owada, Misao, Ohashi, Toya, Kobayashi, Masahisa, Eto, Yoshikatsu, Tanaka, Akemi, Mills, Kevin, Winchester, Bryan, Keutzer, Joan

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Frequency of de novo mutations in Japanese patients with Fabry disease von Kobayashi, Masahisa, Ohashi, Toya, Iizuka, Sayoko, Kaneshiro, Eiko, Higuchi, Takashi, Eto, Yoshikatsu, Ida, Hiroyuki

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Selective bronchial occlusion as treatment for pulmonary interstitial emphysema von Inage, Yuka, Kumazawa, Kensuke, Mori, Takuma, Tanabe, Yukitoshi, Kobayashi, Masahisa

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