Globotriaosylceramide Immunostaining of Myocardium in a Patient With Fabry Disease von Yoshida, Satoru, Kawano, Hiroaki, Ikeda, Satoshi, Sakuraba, Hitoshi, Okano, Shinji, Maemura, Koji

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Profiles of Globotriaosylsphingosine Analogs and Globotriaosylceramide Isoforms Accumulated in Body Fluids from Various Phenotypic Fabry Patients von Shiga, Tomoko, Tsukimura, Takahiro, Kubota, Takao, Togawa, Tadayasu, Sakuraba, Hitoshi

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High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening von Spada, Marco, Pagliardini, Severo, Yasuda, Makiko, Tukel, Turgut, Thiagarajan, Geetha, Sakuraba, Hitoshi, Ponzone, Alberto, Desnick, Robert J.

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Comparative study on incorporation of three recombinant human α-galactosidase A drugs (agalsidases) into cultured fibroblasts and organs/tissues of Fabry mice von Tsukimura, Takahiro, Shiga, Tomoko, Togawa, Tadayasu, Sakuraba, Hitoshi

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Nano-LC-MS/MS for Quantification of Lyso-Gb3 and Its Analogues Reveals a Useful Biomarker for Fabry Disease von Sueoka, Hideaki, Ichihara, Junji, Tsukimura, Takahiro, Togawa, Tadayasu, Sakuraba, Hitoshi

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Structural Basis of Mucopolysaccharidosis Type II and Construction of a Database of Mutant Iduronate 2-Sulfatases von Saito, Seiji, Ohno, Kazuki, Okuyama, Torayuki, Sakuraba, Hitoshi

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Distributions of Globotriaosylceramide Isoforms, and Globotriaosylsphingosine and Its Analogues in an α-Galactosidase A Knockout Mouse, a Model of Fabry Disease von Sueoka, Hideaki, Aoki, Mikio, Tsukimura, Takahiro, Togawa, Tadayasu, Sakuraba, Hitoshi

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Inhibition of astrocytic adenosine receptor A2A attenuates microglial activation in a mouse model of Sandhoff disease von Ogawa, Yasuhiro, Furusawa, Eiri, Saitoh, Takahiro, Sugimoto, Hiroki, Omori, Takumi, Shimizu, Shinya, Kondo, Hisatsugu, Yamazaki, Mika, Sakuraba, Hitoshi, Oishi, Kazuhiko

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In Vivo Delivery of Therapeutic Molecules by Transplantation of Genome-Edited Induced Pluripotent Stem Cells von Nakajima, Ittetsu, Tsukimura, Takahiro, Ono, Terumi, Shiga, Tomoko, Shitara, Hiroshi, Togawa, Tadayasu, Sakuraba, Hitoshi, Miyaoka, Yuichiro

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Genetically Modified Cell Transplantation Through Macroencapsulated Spheroids with Scaffolds to Treat Fabry Disease von Kami, Daisuke, Suzuki, Yosuke, Yamanami, Masashi, Tsukimura, Takahiro, Togawa, Tadayasu, Sakuraba, Hitoshi, Gojo, Satoshi

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Abnormal differentiation of Sandhoff disease model mouse-derived multipotent stem cells toward a neural lineage von Ogawa, Yasuhiro, Kaizu, Katsutoshi, Yanagi, Yusuke, Takada, Subaru, Sakuraba, Hitoshi, Oishi, Kazuhiko

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Fabry-database.org: database of the clinical phenotypes, genotypes and mutant α-galactosidase A structures in Fabry disease von Saito, Seiji, Ohno, Kazuki, Sakuraba, Hitoshi

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Abnormal organization during neurodevelopment in a mouse model of Sandhoff disease von Ogawa, Yasuhiro, Sasanuma, Yayoi, Shitara, Shuhei, Koshizuka, Asuna, Okada, Rieko, Sakuraba, Hitoshi, Oishi, Kazuhiko

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Does administration of hydroxychloroquine/amiodarone affect the efficacy of enzyme replacement therapy for Fabry mice? von Tsukimura, Takahiro, Saito, Koki, Shiga, Tomoko, Ogawa, Yasuhiro, Sakuraba, Hitoshi, Togawa, Tadayasu

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Plasma globotriaosylsphingosine as a biomarker of Fabry disease von Togawa, Tadayasu, Kodama, Takashi, Suzuki, Toshihiro, Sugawara, Kanako, Tsukimura, Takahiro, Ohashi, Toya, Ishige, Nobuyuki, Suzuki, Ken, Kitagawa, Teruo, Sakuraba, Hitoshi

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Cell Transplantation Combined with Recombinant Collagen Peptides for the Treatment of Fabry Disease von Kami, Daisuke, Yamanami, Masashi, Tsukimura, Takahiro, Maeda, Hideki, Togawa, Tadayasu, Sakuraba, Hitoshi, Gojo, Satoshi

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Monitoring of anti-drug antibodies and disease-specific biomarkers in three patients from a Japanese Fabry family treated with enzyme replacement therapy von Kubota, Takao, Tsukimura, Takahiro, Shiga, Tomoko, Togawa, Tadayasu, Sakuraba, Hitoshi

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Comparative urinary globotriaosylceramide analysis by thin-layer chromatography-immunostaining and liquid chromatography-tandem mass spectrometry in patients with Fabry disease von Shiga, Tomoko, Tsukimura, Takahiro, Namai, Yurie, Togawa, Tadayasu, Sakuraba, Hitoshi

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Late-onset Krabbe disease is predominant in Japan and its mutant precursor protein undergoes more effective processing than the infantile-onset form von Hossain, Mohammad Arif, Otomo, Takanobu, Saito, Seiji, Ohno, Kazuki, Sakuraba, Hitoshi, Hamada, Yusuke, Ozono, Keiichi, Sakai, Norio

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Comparative study of structural changes caused by different substitutions at the same residue on α-galactosidase A von Saito, Seiji, Ohno, Kazuki, Sakuraba, Hitoshi

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