AAAAAA

   
Results: 1-25 | 26-34 |
Results: 26-34/34

Authors: Kurata, K Hayashi, M Satoh, J Kojima, H Nagata, J Tamagawa, K Shinohara, T Morimatsu, Y Kominami, E
Citation: K. Kurata et al., Pathological study on sibling autopsy cases of the late infantile form of neuronal ceroid lipofuscinosis, BRAIN DEVEL, 21(1), 1999, pp. 63-67

Authors: Fukuzawa, M Satoh, J Qiang, X Miyaguchi, S Sakata, Y Nakazawa, T Ikehata, F Ohta, S Toyota, T
Citation: M. Fukuzawa et al., Inhibition of tumor necrosis factor-alpha with anti-diabetic agents, DIABET RE C, 43(3), 1999, pp. 147-154

Authors: Kutsuwada, K Satoh, J Ohki, G Muto, S Imai, M Arakawa, M Suzuki, M
Citation: K. Kutsuwada et al., Cloning and characterization of 5 '-flanking region of mouse non-selectivecation channel 1, BBA-GENE ST, 1444(1), 1999, pp. 92-100

Authors: Kastrukoff, LF Morgan, NG Zecchini, D White, R Petkau, AJ Satoh, J Paty, DW
Citation: Lf. Kastrukoff et al., Natural killer cells in relapsing-remitting MS - Effect of treatment with interferon beta-1B, NEUROLOGY, 52(2), 1999, pp. 351-359

Authors: Satoh, J
Citation: J. Satoh, Sums of products of two q-Bernoulli numbers, J NUMBER TH, 74(2), 1999, pp. 173-180

Authors: Negoro, K Kinouchi, Y Hiwatashi, N Takahashi, S Takagi, S Satoh, J Shimosegawa, T Toyota, T
Citation: K. Negoro et al., Crohn's disease is associated with novel polymorphisms in the 5 '-flankingregion of the tumor necrosis factor gene, GASTROENTY, 117(5), 1999, pp. 1062-1068

Authors: Satoh, J Kurohara, K Yukitake, M Kuroda, Y
Citation: J. Satoh et al., The 14-3-3 protein detectable in the cerebrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture, EUR NEUROL, 41(4), 1999, pp. 216-225

Authors: Mushiake, K Arimoto, M Satoh, J Mori, K
Citation: K. Mushiake et al., Detection of PRDV from wild adult kuruma prawn, FISH PATHOL, 33(5), 1998, pp. 503-509

Authors: Satoh, J Kuroda, Y Nawata, H Yanase, T
Citation: J. Satoh et al., Molecular basis of hypokalemic myopathy caused by 17 alpha-hydroxylase/17,20-lyase deficiency, NEUROLOGY, 51(6), 1998, pp. 1748-1751
Risultati: 1-25 | 26-34 |