Scalpellum occulta: A rare case of dorsal spinal arachnoid web without the scalpel sign von Choi, Joo Won, DeSimone, Kulani E., Dacumos, Vianca Mae, Hoshide, Reid R., Qiao, Yang, Hui, Ferdinand K.

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Concurrence of chromosome 6 chromothripsis and glioblastoma metastasis von Rennert, Robert C, Hoshide, Reid R, Signorelli, Jason W, Amaro, Deirdre, Sack, Jayson A, Brennan, Cameron W, Chen, Clark C

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Prenatal monitoring of ornithine transcarbamoylase deficiency in two families by DNA analysis von Matsuura, T., Hoshide, R., Fukushima, M., Sakiyama, T., Owada, M., Matsuda, I.

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Identification of two new aberrant splicings in the ornithine carbamoyltransferase (OCT) gene in two patients with early and late onset OCT deficiency von Matsuura, T., Hoshide, R., Komaki, S., Kiwaki, K., Endo, F., Nakamura, S., Jitosho, T., Matsuda, I.

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Specificity of PCR‐SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency von Hoshide, R., Matsuura, T., Komaki, S., Koike, E., Ueno, I., Matsuda, I.

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Emergence of community-acquired extended-spectrum beta-lactamase Escherichia coli (ESBLEC) in Honolulu: a case series of three individuals with community-acquired ESBLEC bacteriuri... von Hoshide, Reid R, Chung, Heath, Tokeshi, Jinichi

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The polymorphic 43Thr bcl-2 protein confers relative resistance to autoimmunity : an analytical evaluation von KOMAKI, S, KOHNO, M, MATSUURA, N, SHIMADZU, M, ADACHI, N, HOSHIDE, R, NISHIYAMA, S, MATSUDA, I

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Barriers to healthcare of homeless residents of three Honolulu shelters von Hoshide, Reid R, Manog, Jenny D, Noh, Thomas, Omori, Jill

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Molecular Cloning, Tissue Distribution, and Chromosomal Localization of Human Cationic Amino Acid Transporter 2 (HCAT2) von Hoshide, Ryuuji, Ikeda, Yoichiro, Karashima, Shinnyo, Matsuura, Toshinobu, Komaki, Satoru, Kishino, Tatsuya, Niikawa, Norio, Endo, Fumio, Matsuda, Ichiro

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Favorable outcomes for Native Hawaiians and other Pacific Islanders with severe traumatic brain injury von Nakagawa, Kazuma, Hoshide, Reid R, Asai, Susan M, Johnson, Katherine G, Beniga, Juliet G, Albano, Melanie C, del Castillo, Johnna L, Donovan, Daniel J, Chang, Cherylee W, Koenig, Matthew A

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Ten novel mutations of the ornithine transcarbamylase (OTC) gene in OTC deficiency von Shimadzu, Mitsunobu, Matsumoto, Hiroshi, Matsuura, Toshinobu, Kobayashi, Keiko, Komaki, Satoru, Kiwaki, Kohji, Hoshide, Ryuuji, Endo, Fumio, Saheki, Takeyori, Matsuda, Ichiro

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Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomati... von Matsuda, I, Matsuura, T, Nishiyori, A, Komaki, S, Hoshide, R, Matsumoto, T, Funakoshi, M, Kiwaki, K, Endo, F, Hata, A, Shimadzu, M, Yoshino, M

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For novel gene mutations in five Japanese male patients with neonatal or late onset OTC deficiency : application of PCR-single-strand conformation polymorphisms for all exons and a... von MATSUURA, T, HOSHIDE, R, SETOYAMA, C, SHIMADA, K, HASE, Y, YANAGAWA, T, KAJITA, M, MATSUDA, I

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The R40h mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients von NISHIYORI, A, YOSHINO, M, MORI, M, KATO, H, MATSUURA, T, HOSHIDE, R, MATSUDA, I, KUNO, T, MIYAZAKI, S, HIROSE, S.-I, KUROMARU, R.-I

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Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male von Nishiyori, Atsushi, Yoshino, Makoto, Tananari, Yoshifumi, Matsuura, Toshinobu, Hoshide, Ryuuji, Mastuda, Ichiro, Mori, Masataka, Kato, Hirohisa

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Carbamyl phosphate synthetase I deficiency : one base substitution in an exon of the CPS I gene causes a 9-basepair deletion due to aberrant splicing von HOSHIDE, R, MATSUURA, T, HARAGUCHI, Y, ENDO, F, YOSHINAGA, M, MATSUDA, I

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Scalpellum occulta: A rare case of dorsal spinal arachnoid web without the scalpel sign von Choi, Joo Won, DeSimone, Kulani E, Dacumos, Vianca Mae, Hoshide, Reid R, Qiao, Yang, Hui, Ferdinand K

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Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male von Nishiyori, A, Yoshino, M, Tananari, Y, Matsuura, T, Hoshide, R, Mastuda, I, Mori, M, Kato, H

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Assignment of the Human Carbamyl Phosphate Synthetase I Gene (CPS1) to 2q35 by Fluorescence in Situ Hybridization von Hoshide, Ryuuji, Soejima, Hidenobu, Ohta, Tohru, Niikawa, Norio, Haraguchi, Yougo, Matsuura, Toshinobu, Endo, Fumio, Matsuda, Ichiro

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Ten novel mutations of the ornithine transcarbamylase (OTC) gene in OTC deficiency von Shimadzu, M, Matsumoto, H, Matsuura, T, Kobayashi, K, Komaki, S, Kiwaki, K, Hoshide, R, Endo, F, Saheki, T, Matsuda, I

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