Analysis of respiratory movement in the spondylotic myelopathy at middle-low cervical level von Oguni, E, Nagata, H

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Spatial patterns of reflex evoked by pressure stimulation of the foot pads in cats von Hongo, T, Kudo, N, Oguni, E, Yoshida, K

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Amyloid β protein in plasma from patients with sporadic Alzheimer's disease von Tamaoka, Akira, Fukushima, Tetsuo, Sawamura, Naoya, Ishikawa, Kin'ya, Oguni, Eiichi, Komatsuzaki, Yasuko, Shoji, Shin'ichi

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Dose-dependent association of apolipoprotein E allele epsilon 4 with late-onset, sporadic Alzheimer's disease von Yoshizawa, T, Yamakawa-Kobayashi, K, Komatsuzaki, Y, Arinami, T, Oguni, E, Mizusawa, H, Shoji, S, Hamaguchi, H

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Clinical evaluation of plasma exchange and high dose intravenous immunoglobulin in a patient with Isaacs' syndrome von Ishii, A, Hayashi, A, Ohkoshi, N, Oguni, E, Maeda, M, Ueda, Y, Ishii, K, Arasaki, K, Mizusawa, H, Shoji, S

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Prion disease with 144 base pair insertion in a Japanese family line von ODA, T, KITAMOTO, T, KASHIMA, H, KOGURE, T, HORI, K, OGINO, K, TATEISHI, J, MITSUHASHI, T, IWABUCHI, K, HAGA, C, OGUNI, E, KATO, Y, TOMINAGA, I, YANAI, K

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Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group von Klepper, Joerg, Akman, Cigdem, Armeno, Marisa, Auvin, Stéphane, Cervenka, Mackenzie, Cross, Helen J., De Giorgis, Valentina, Della Marina, Adela, Engelstad, Kristin, Heussinger, Nicole, Kossoff, Eric H., Leen, Wilhelmina G., Leiendecker, Baerbel, Monani, Umrao R., Oguni, Hirokazu, Neal, Elizabeth, Pascual, Juan M., Pearson, Toni S., Pons, Roser, Scheffer, Ingrid E., Veggiotti, Pierangelo, Willemsen, Michél, Zuberi, Sameer M., De Vivo, Darryl C.

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Variant Intestinal-Cell Kinase in Juvenile Myoclonic Epilepsy von Bailey, Julia N, de Nijs, Laurence, Bai, Dongsheng, Suzuki, Toshimitsu, Miyamoto, Hiroyuki, Tanaka, Miyabi, Patterson, Christopher, Lin, Yu-Chen, Medina, Marco T, Alonso, María E, Serratosa, José M, Durón, Reyna M, Nguyen, Viet H, Wight, Jenny E, Martínez-Juárez, Iris E, Ochoa, Adriana, Jara-Prado, Aurelio, Guilhoto, Laura, Molina, Yolly, Yacubian, Elsa M, López-Ruiz, Minerva, Inoue, Yushi, Kaneko, Sunao, Hirose, Shinichi, Osawa, Makiko, Oguni, Hirokazu, Fujimoto, Shinji, Grisar, Thierry M, Stern, John M, Yamakawa, Kazuhiro, Lakaye, Bernard, Delgado-Escueta, Antonio V

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Mutations in EFHC1 cause juvenile myoclonic epilepsy von Delgado-Escueta, Antonio V, Yamakawa, Kazuhiro, Suzuki, Toshimitsu, Aguan, Kripamoy, Alonso, Maria E, Shi, Jun, Hara, Yuji, Nishida, Motohiro, Numata, Tomohiro, Medina, Marco T, Takeuchi, Tamaki, Morita, Ryoji, Bai, Dongsheng, Ganesh, Subramaniam, Sugimoto, Yoshihisa, Inazawa, Johji, Bailey, Julia N, Ochoa, Adriana, Jara-Prado, Aurelio, Rasmussen, Astrid, Ramos-Peek, Jaime, Cordova, Sergio, Rubio-Donnadieu, Francisco, Inoue, Yushi, Osawa, Makiko, Kaneko, Sunao, Oguni, Hirokazu, Mori, Yasuo

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Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy von MEDINA, M. T, SUZUKI, T, MONTOYA, M. C, OCHOA, A, JARA PRADO, A, TANAKA, M, MACHADO-SALAS, J, FUJIMOTO, S, ITO, M, HAMANO, S, SUGITA, K, UEDA, Y, ALONSO, M. E, OSAWA, M, OGUNI, H, RUBIO-DONNADIEU, F, YAMAKAWA, K, DELGADO-ESCUETA, A. V, DURON, R. M, MARTINEZ-JUAREZ, I. E, BAILEY, J. N, BAI, D, INOUE, Y, YOSHIMURA, I, KANEKO, S

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Congenital malformations due to antiepileptic drugs von Kaneko, S, Battino, D, Andermann, E, Wada, K, Kan, R, Takeda, A, Nakane, Y, Ogawa, Y, Avanzini, G, Fumarola, C, Granata, T, Molteni, F, Pardi, G, Minotti, L, Canger, R, Dansky, L, Oguni, M, Lopes-Cendas, I, Sherwin, A, Andermann, F, Seni, M.-H, Okada, M, Teranishi, T

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TULIP1 ( RALGAPA1) haploinsufficiency with brain development delay von Shimojima, Keiko, Komoike, Yuta, Tohyama, Jun, Takahashi, Sonoko, Páez, Marco T., Nakagawa, Eiji, Goto, Yuichi, Ohno, Kousaku, Ohtsu, Mayu, Oguni, Hirokazu, Osawa, Makiko, Higashinakagawa, Toru, Yamamoto, Toshiyuki

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Densin-180 Forms a Ternary Complex with the α-Subunit of Ca2+/Calmodulin-Dependent Protein Kinase II and α-Actinin von Walikonis, Randall S., Oguni, Asako, Khorosheva, Eugenia M., Jeng, Chung-Jiuan, Asuncion, Franklin J., Kennedy, Mary B.

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Positional Cloning of the Gene LIMBIN Responsible for Bovine Chondrodysplastic Dwarfism von Takeda, Haruko, Takami, Marika, Oguni, Tomoko, Tsuji, Takehito, Yoneda, Kazuhiro, Sato, Hiroaki, Ihara, Naoya, Itoh, Tomohito, Kata, Srinivas R., Mishina, Yuji, Womack, James E., Moritomo, Yasuo, Sugimoto, Yoshikazu, Kunieda, Tetsuo

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Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online von Singh, Baljinder, Monteil, Arnaud, Bidaud, Isabelle, Sugimoto, Yoshihisa, Suzuki, Toshimitsu, Hamano, Shin-ichiro, Oguni, Hirokazu, Osawa, Makiko, Alonso, Maria E, Delgado-Escueta, Antonio V, Inoue, Yushi, Yasui-Furukori, Norio, Kaneko, Sunao, Lory, Philippe, Yamakawa, Kazuhiro

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Successive phase transitions of [(PyO)(H/D)][AuCl 4] (PyO=C 5H 5NO) von Asaji, Tetsuo, Watanabe, Jun, Akiyama, Eigo, Fujimori, Hiroki, Oguni, Masaharu

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Acquired epileptiform opercular syndrome: a case report and results of single photon emission computed tomography and computer-assisted electroencephalographic analysis von Tachikawa, Emiko, Oguni, Hirokazu, Shirakawa, Seigo, Funatsuka, Makoto, Hayashi, Kitami, Osawa, Makiko

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Liquid fragility and the glass transition in water and aqueous solutions von Angell, C.A., Bressel, R.D., Green, J.L., Kanno, H., Oguni, M., Sare, E.J.

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Intrauterine growth in the offspring of epileptic women: a prospective multicenter study von Battino, D, Kaneko, S, Andermann, E, Avanzini, G, Canevini, M.P, Canger, R, Croci, D, Fumarola, C, Guidolin, L, Mamoli, D, Molteni, F, Pardi, G, Vignoli, A, Fukushima, Y, Kan, R, Takeda, A, Nakane, Y, Ogawa, Y, Dansky, L, Oguni, M, Lopez-Ciendas, I, Sherwin, A, Andermann, F, Seni, M.-H, Otani, K, Teranishi, T, Goto, M

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FAIXA DE ACETATO DE CELULOSE FORMADO DE FIBRAS DE ACETATO DE CELULOSE, MÉTODO PARA PRODUÇÃO DE UMA FAIXA DE ACETATO DE CELULOSE von KAZUMA OGUNI

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