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Results:
1-16
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Results: 16
Authors:
Ozawa, E
Nishino, I
Nonaka, I
Citation: E. Ozawa et al., Sarcolemmopathy: Muscular dystrophies with cell membrane defects, BRAIN PATH, 11(2), 2001, pp. 218-230
Authors:
Matsuda, C
Hayashi, YK
Ogawa, M
Aoki, M
Murayama, K
Nishino, I
Nonaka, I
Arahata, K
Brown, RH
Citation: C. Matsuda et al., The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle, HUM MOL GEN, 10(17), 2001, pp. 1761-1766
Authors:
Nishino, I
Spinazzola, A
Hirano, M
Citation: I. Nishino et al., MNGIE: from nuclear DNA to mitochondrial DNA, NEUROMUSC D, 11(1), 2001, pp. 7-10
Authors:
Shirasaki, T
Nishino, I
Yamamoto, K
Citation: T. Shirasaki et al., Determination of vanadium, chromium, arsenic, selenium and molybdenum in river and lake-water samples by nitrogen microwave-induced plasma mass spectrometry, BUNSEKI KAG, 50(9), 2001, pp. 595-601
Authors:
Ikemoto-Tsuchiya, K
Nishino, I
Kawai, M
Morimatsu, M
Nonaka, I
Citation: K. Ikemoto-tsuchiya et al., A new form of muscular dystrophy with mitochondrial structural abnormalities, MUSCLE NERV, 24(12), 2001, pp. 1710-1711
Authors:
Nishino, I
Fujitomo, H
Umeda, T
Citation: I. Nishino et al., Determination of a new oral cephalosporin, cefmatilen hydrochloride hydrate, and its seven metabolites in human and animal plasma and urine by coupled systems of ion-exchange and reversed-phase high-performance liquid chromatography, J CHROMAT B, 749(1), 2000, pp. 101-110
Authors:
Nishino, I
Spinazzola, A
Papadimitriou, A
Hammans, S
Steiner, I
Hahn, CD
Connolly, AM
Verloes, A
Guimaraes, J
Maillard, I
Hamano, H
Donati, MA
Semrad, CE
Russell, JA
Andreu, AL
Hadjigeorgiou, GM
Vu, TH
Tadesse, S
Nygaard, TG
Nonaka, I
Hirano, I
Bonilla, E
Rowland, LP
DiMauro, S
Hirano, M
Citation: I. Nishino et al., Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations, ANN NEUROL, 47(6), 2000, pp. 792-800
Authors:
Amemiya, S
Hamamoto, M
Goto, Y
Komaki, H
Nishino, I
Nonaka, I
Katayama, Y
Citation: S. Amemiya et al., Psychosis and progressing dementia: Presenting features of a mitochondriopathy, NEUROLOGY, 55(4), 2000, pp. 600-601
Authors:
Nishino, I
Fu, J
Tanji, K
Yamada, T
Shimojo, S
Koori, T
Mora, M
Riggs, JE
Oh, SJ
Koga, Y
Sue, CM
Yamamoto, A
Murakami, N
Shanske, S
Byrne, E
Bonilla, E
Nonaka, I
DiMauro, S
Hirano, M
Citation: I. Nishino et al., Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease), NATURE, 406(6798), 2000, pp. 906-910
Authors:
Fujitomo, H
Nagaoka, T
Nishino, I
Umeda, T
Citation: H. Fujitomo et al., Determination of a new oral cephalosporin, S-1090, in human plasma and urine by direct injection high-performance liquid chromatography with ultraviolet detection and column switching, J CHROMAT B, 728(1), 1999, pp. 125-131
Authors:
Papadopoulou, LC
Sue, CM
Davidson, MM
Tanji, K
Nishino, I
Sadlock, JE
Krishna, S
Walker, W
Selby, J
Glerum, DM
Van Coster, R
Lyon, G
Scalais, E
Lebel, R
Kaplan, P
Shanske, S
De Vivo, DC
Bonilla, E
Hirano, M
DiMauro, S
Schon, EA
Citation: Lc. Papadopoulou et al., Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene, NAT GENET, 23(3), 1999, pp. 333-337
Authors:
Nygaard, TG
Raymond, D
Chen, CP
Nishino, I
Greene, PE
Jennings, D
Heiman, GA
Klein, C
Saunders-Pullman, RJ
Kramer, P
Ozelius, LJ
Bressman, SB
Citation: Tg. Nygaard et al., Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31, ANN NEUROL, 46(5), 1999, pp. 794-798
Authors:
Nishino, I
Spinazzola, A
Hirano, M
Citation: I. Nishino et al., Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder, SCIENCE, 283(5402), 1999, pp. 689-692
Authors:
Sue, CM
Tanji, K
Hadjigeorgiou, G
Andreu, AL
Nishino, I
Krishna, S
Bruno, C
Hirano, M
Shanske, S
Bonilla, E
Fischel-Ghodsian, N
DiMauro, S
Friedman, R
Citation: Cm. Sue et al., Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene, NEUROLOGY, 52(9), 1999, pp. 1905-1908
Authors:
Minami, N
Nishino, I
Kobayashi, O
Ikezoe, K
Goto, Y
Nonaka, I
Citation: N. Minami et al., Mutations of calpain 3 gene in patients with sporadic limb-girdle musculardystrophy in Japan, J NEUR SCI, 171(1), 1999, pp. 31-37
Authors:
Kimura, S
Sugino, S
Ohtani, Y
Matsukura, M
Nishino, I
Ikezawa, M
Sakata, A
Kondo, Y
Yoshioka, K
Huard, J
Nonaka, I
Miike, T
Citation: S. Kimura et al., Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy, ANN NEUROL, 44(6), 1998, pp. 967-971
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