Yosuke Kokunai
Osaka, Japan
Last Updated: 09/26/2026
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Found 8 publications
Hypokalaemic periodic paralysis with a charge-retaining substitution in the voltage sensor.
Journal: Brain communications
Published: May 26, 2020
A204E mutation in Nav1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs.
Journal: Scientific reports
Published: July 27, 2018
A case of non-dystrophic myotonia with concomitant mutations in the SCN4A and CLCN1 genes.
Journal: Journal of the neurological sciences
Published: August 25, 2015
A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.
Journal: Neurology
Published: February 28, 2014
Compound heterozygous mutations in the muscle chloride channel gene (CLCN1) in a Japanese family with Thomsen's disease
Journal: Rinsho shinkeigaku = Clinical neurology
Published: April 23, 2013
A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravis.
Journal: Neuroscience letters
Published: February 09, 2012
A survey of cardiologists, diabetologists, gynecologists and ophthalmologists practicing in Osaka on the medical consultation behaviors of myotonic dystrophy patients
Journal: Rinsho shinkeigaku = Clinical neurology
Published: September 28, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026