International Morquio A Registry: Clinical manifestation and natural course of Morquio A disease von Montaño, A. M., Tomatsu, S., Gottesman, G. S., Smith, M., Orii, T.

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Effect of ‘attenuated' mutations in mucopolysaccharidosis IVA on molecular phenotypes of N-acetylgalactosamine-6-sulfate sulfatase von Montaño, A. M, Sukegawa, K, Kato, Z, Carrozzo, R, Di Natale, P, Christensen, E, Orii, K. O, Orii, T, Kondo, N, Tomatsu, S

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Mucopolysaccharidosis IVA: identification of mutations and methylation study in GALNS gene von Tomatsu, S, Nishioka, T, Montaño, A M, Gutierrez, M A, Pena, O S, Orii, K O, Sly, W S, Yamaguchi, S, Orii, T, Paschke, E, Kircher, S G, Noguchi, A

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Natural history of extensive Mongolian spots in mucopolysaccharidosis type II (Hunter syndrome): a survey among 52 Japanese patients von Ochiai, T, Suzuki, Y, Kato, T, Shichino, H, Chin, M, Mugishima, H, Orii, T

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Effect of Hunter disease (mucopolysaccharidosis type II) mutations on molecular phenotypes of iduronate‐2‐sulfatase: Enzymatic activity, protein processing and structural analysis... von Sukegawa‐Hayasaka, K., Kato, Z., Nakamura, H., Tomatsu, S., Fukao, T., Kuwata, K., Orii, T., Kondo, N.

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Effect of insitu annealing on physical properties of Si nanoparticles synthesized by pulsed laser ablation von HIRASAWA, M, ORII, T, SETO, T

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Keratan sulphate levels in mucopolysaccharidoses and mucolipidoses von Tomatsu, S., Okamura, K., Maeda, H., Taketani, T., Castrillon, S. V., Gutierrez, M. A., Nishioka, T., Fachel, A. A., Orii, K. O., Grubb, J. H., Cooper, A., Thornley, M., Wraith, E., Barrera, L. A., Laybauer, L. S., Giugliani, R., Schwartz, I. V., Frenking, G. Schulze, Beck, M., Kircher, S. G., Paschke, E., Yamaguchi, S., Ullrich, K., Haskins, M., Isogai, K., Suzuki, Y., Orii, T., Kondo, N., Creer, M., Okuyama, T., Tanaka, A., Noguchi, A.

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Heparan sulfate levels in mucopolysaccharidoses and mucolipidoses von Tomatsu, S., Gutierrez, M. A., Ishimaru, T., Peña, O. M., Montaño, A. M., Maeda, H., Velez‐Castrillon, S., Nishioka, T., Fachel, A. A., Cooper, A., Thornley, M., Wraith, E., Barrera, L. A., Laybauer, L. S., Giugliani, R., Schwartz, I. V., Frenking, G. Schulze, Beck, M., Kircher, S. G., Paschke, E., Yamaguchi, S., Ullrich, K., Isogai, K., Suzuki, Y., Orii, T., Noguchi, A.

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Growth of single-walled carbon nanotubes from size-selected catalytic metal particles von KOHNO, M, ORII, T, HIRASAWA, M, SETO, T, MURAKAMI, Y, CHIASHI, S, MIYAUCHI, Y, MARUYAMA, S

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Hematopoietic Stem Cell Transplantation for Mucopolysaccharidoses: Past, Present, and Future von Taylor, Madeleine, Khan, Shaukat, Stapleton, Molly, Wang, Jianmin, Chen, Jing, Wynn, Robert, Yabe, Hiromasa, Chinen, Yasutsugu, Boelens, Jaap Jan, Mason, Robert W., Kubaski, Francyne, Horovitz, Dafne D.G., Barth, Anneliese L., Serafini, Marta, Bernardo, Maria Ester, Kobayashi, Hironori, Orii, Kenji E., Suzuki, Yasuyuki, Orii, Tadao, Tomatsu, Shunji

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Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase von Izai, K, Uchida, Y, Orii, T, Yamamoto, S, Hashimoto, T

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Cloning of a human gene, PIG-F, a component of glycosylphosphatidylinositol anchor biosynthesis, by a novel expression cloning strategy von Inoue, N, Kinoshita, T, Orii, T, Takeda, J

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Treatment of MPS VII (Sly disease) by allogeneic BMT in a female with homozygous A619V mutation von YAMADA, Y, KATO, K, ORII, T, SUKEGAWA, K, TOMATSU, S, FUKUDA, S, EMURA, S, KOJIMA, S, MATSUYAMA, T, SLY, W. S, KONDO, N

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Human peroxisome assembly factor-2 (PAF-2) : A gene responsible for group C peroxisome biogenesis disorder in humans von FUKUDA, S, SHIMOZAWA, N, KUROKI, Y, FUJIKI, Y, ORII, T, KONDO, N, SUZUKI, Y, ZHANG, Z, TOMATSU, S, TSUKAMOTO, T, HASHIGUCHI, N, OSUMI, T, MASUNO, M, IMAIZUMI, K

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Optical excitation and energy transfer of Eu3+-doped CdS nanocrystals in reverse micelles von Matsuishi, K, Makita, Y, Onari, S, Orii, T, Seto, A

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Temperature dependence of photoluminescence from mono-dispersed Si nanoparticles von ORII, T, HIRASAWA, M, SETO, T, AYA, N, ONARI, S

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Purification and Properties of Rat Liver Peroxisomal Very-Long-Chain Acyl-CoA Synthetase von Uchida, Yasushi, Kondo, Naomi, Orii, Tadao, Hashimoto, Takashi

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Magnetic Properties of Monodispersed Ni/NiO Core−Shell Nanoparticles von Seto, Takafumi, Akinaga, Hiroyuki, Takano, Fumiyoshi, Koga, Kenji, Orii, Takaaki, Hirasawa, Makoto

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Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders von Suzuki, Y., Shimozawa, N., Imamura, A., Fukuda, S., Zhang, Z., Orii, T., Kondo, N.

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Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect von Shimozawa, N, Suzuki, Y, Orii, T, Moser, A, Moser, H W, Wanders, R J

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