Masanori Takahashi
Affiliations: | Neurology | Osaka Univ, Suita-shi, Ōsaka-fu, Japan |
Area:
neuromuscular disordersGoogle:
"Masanori Takahashi"Mean distance: 15.86 (cluster 6) | S | N | B | C | P |
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Publications
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| Kubota T, Takahashi S, Yamamoto R, et al. (2023) Optical measurement of gating pore currents in hypokalemic periodic paralysis model cells. Disease Models & Mechanisms |
| Segawa K, Nishiyama M, Mori I, et al. (2023) Hyperkalemic periodic paralysis associated with a novel missense variant located in the inner pore of Nav1.4. Brain & Development |
| Shibano M, Kubota T, Kokubun N, et al. (2022) Periodic paralysis due to cumulative effects of rare variants in SCN4A with small functional alterations. Muscle & Nerve |
| Kubota T, Wu F, Vicart S, et al. (2020) Hypokalaemic periodic paralysis with a charge-retaining substitution in the voltage sensor. Brain Communications. 2: fcaa103 |
| Kubota T, Nakamori M, Takahashi MP. (2014) [Myotonia and cardiac conduction defects in myotonic dystrophy and defect in ion channels]. Rinsho Byori. the Japanese Journal of Clinical Pathology. 62: 246-54 |
| Kokunai Y, Nakata T, Furuta M, et al. (2014) A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1. Neurology. 82: 1058-64 |
| Kokunai Y, Goto K, Kubota T, et al. (2012) A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravis. Neuroscience Letters. 519: 67-72 |
| Yoshinaga H, Sakoda S, Good JM, et al. (2012) A novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodes. Journal of the Neurological Sciences. 315: 15-9 |
| Kubota T, Roca X, Kimura T, et al. (2011) A mutation in a rare type of intron in a sodium-channel gene results in aberrant splicing and causes myotonia. Human Mutation. 32: 773-82 |
| Kubota T, Kinoshita M, Sasaki R, et al. (2009) New mutation of the Na channel in the severe form of potassium-aggravated myotonia. Muscle & Nerve. 39: 666-73 |