Search Results - "Tsuyusaki, Y."

Molecular genetic analysis of 30 families with Joubert syndrome by Suzuki, T., Miyake, N., Tsurusaki, Y., Okamoto, N., Alkindy, A., Inaba, A., Sato, M., Ito, S., Muramatsu, K., Kimura, S., Ieda, D., Saitoh, S., Hiyane, M., Suzumura, H., Yagyu, K., Shiraishi, H., Nakajima, M., Fueki, N., Habata, Y., Ueda, Y., Komatsu, Y., Yan, K., Shimoda, K., Shitara, Y., Mizuno, S., Ichinomiya, K., Sameshima, K., Tsuyusaki, Y., Kurosawa, K., Sakai, Y., Haginoya, K., Kobayashi, Y., Yoshizawa, C., Hisano, M., Nakashima, M., Saitsu, H., Takeda, S., Matsumoto, N.

“…Joubert syndrome (JS) is rare recessive disorders characterized by the combination of hypoplasia/aplasia of the cerebellar vermis, thickened and elongated…”
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Tolterodine activates the frontal micturition area of OAB patients: A real-time measure of oxyhemoglobin concentration changes during urodynamics by Sakakibara, R, Tateno, F, Kishi, M, Tsuyusaki, Y, Yamamoto, T, Uchiyama, T, Takahashi, O

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Meningitis-retention syndrome” - a urodynamic & clinical analysis by Sakakibara, R, Sugiyama, M, Tateno, F, Yano, M, Takahashi, O, Kishi, M, Tsuyusaki, Y, Yamamoto, T, Yamanishi, T, Uchiyama, T, Shibata, C, Yanagisawa, M

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Antithrombotic-free but dangerous: Post-surgical consideration by Aiba, Y., Sakakibara, R., Tsuyusaki, Y., Tateno, F., Kishi, M., Ogata, T.

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Gatrointestinal dysfunction in dementia with lewy bodies: A comparison with Parkinson’s disease by Sakakibara, R., Doi, H., Tateno, F., Kishi, M., Tsuyusaki, Y., Ogata, T., Aiba, Y.

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Wearable gait sensors to measure degenerative cerebellar ataxia by Sakakibara, R., Terayama, K., Ogawa, A., Haruta, H., Akiba, T., Tateno, F., Kishi, M., Tsuyusaki, Y., Aiba, Y., Ogata, T.

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