Search Results - "AOIKE, F"

Rapid disease progression correlates with instability of mutant SOD1 in familial ALS by Sato, T, Nakanishi, T, Yamamoto, Y, Andersen, P M, Ogawa, Y, Fukada, K, Zhou, Z, Aoike, F, Sugai, F, Nagano, S, Hirata, S, Ogawa, M, Nakano, R, Ohi, T, Kato, T, Nakagawa, M, Hamasaki, T, Shimizu, A, Sakoda, S

“…Studies on the clinical course of familial ALS suggest that the duration of illness is relatively consistent for each mutation but variable among the different…”
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Proton magnetic resonance spectroscopy of a patient with Gerstmann-Straussler-Scheinker disease by KONAKA, K, KAIDO, M, OKUDA, Y, AOIKE, F, ABE, K, KITAMOTO, T, YANAGIHARA, T

“…A 23-year-old woman with Gerstmann-Straussler-Scheinker disease (GSS) was investigated by 1H-magnetic resonance spectroscopy (1H-MRS). She developed gait…”
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Cerebral artery-to-artery embolism in the bay area of metropolitan Osaka, Japan: Frequencies and risk factors by Sugiyama, S., Okuda, Y., Yoshida, T., Kitamura, E., Tanaka, N., Matsubara, Y., Enami, T., Shiraishi, S., Aoike, F., Yanagihara, T.

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Progressive and non-progressive branch atheromatous disease in the bay area of Metropolitan Osaka, Japan: Clinical characteristics by Shiraishi, S., Sugiyama, S., Matsuzaki, J., Yoshida, T., Kitamura, E., Nishida, F., Kuroda, Y., Aoike, F., Okuda, Y., Yanagihara, T.

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Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1 by Kimura, Takashi, Nakamori, Masayuki, Lueck, John D., Pouliquin, Pierre, Aoike, Futoshi, Fujimura, Harutoshi, Dirksen, Robert T., Takahashi, Masanori P., Dulhunty, Angela F., Sakoda, Saburo

“…Myotonic dystrophy type 1 (DM1) is a debilitating multisystemic disorder caused by a CTG repeat expansion in the DMPK gene. Aberrant splicing of several genes…”
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Class Ic antiarrhythmics block human skeletal muscle Na channel during myotonia-like stimulation by Aoike, Futoshi, Takahashi, Masanori P., Sakoda, Saburo

“…Flecainide, a class Ic antiarrhythmic drug, has been anecdotally reported to improve myotonia, but little is known about its kinetics on human skeletal muscle…”
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High rapid disease progression progression correlates with instability of mutant SOD1 in familial ALS by SATO, T, NAKANISHI, T, HIRATA, S, OGAWA, M, NAKANO, R, OHI, T, KATO, T, NAKAGAWA, M, HAMASAKI, T, SHIMIZU, A, SAKODA, S, YAMAMOTO, Y, ANDERSEN, P. M, OGAWA, Y, FUKADA, K, ZHOU, Z, AOIKE, F, SUGAI, F, NAGANO, S

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