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Kazuhiro Yamakawa

18

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1268

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De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies

2019 European Journal of Human Genetics
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Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes

2019 Molecular Medicine
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Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures

2014 Nature Communications
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Ion channels: genetics and as a targets for antiepileptic drugs

2013
- Kazuhiro Yamakawa
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Proposal and Performance Evaluation of a Magneto-Striction Type Torque Sensor Consisting of Small-Sized Coils Connected in Series

2012 International Scholarly Research Notices
- Takahiko Tsujisawa
- Kazuhiro Yamakawa
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305 A non-contact torque sensor system using iterative phase difference detection method

2008
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Nav1.1 Localizes to Axons of Parvalbumin-Positive Inhibitory Interneurons: A Circuit Basis for Epileptic Seizures in Mice Carrying an Scn1a Gene Mutation

2007 The Journal of Neuroscience
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Citations (625)
Mini review Na channel gene mutations in epilepsy—The functional consequences

2006
- Kazuhiro Yamakawa
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Epilepsy and sodium channel gene mutations: gain or loss of function?

2005 Neuroreport
- Kazuhiro Yamakawa
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Citations (29)
[Neurinoma of tympanic plexus: a case report].

2002 Nippon Jibiinkoka Gakkai Kaiho
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