Mio Watanabe
Shibukawa, 3778577, Japan
Last Updated: 09/26/2026
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Found 13 publications
Acute encephalopathy with biphasic seizures and late reduced diffusion; posterior frontal hyperperfusion before late seizures revealed by arterial spin labeling: A case report.
Journal: Brain & development
Published: November 16, 2020
A case of pyridoxine-dependent epilepsy with novel ALDH7A1 mutations.
Journal: Oxford medical case reports
Published: November 17, 2019
Rhinovirus-associated acute encephalitis/encephalopathy and cerebellitis.
Journal: Brain & development
Published: October 28, 2018
Two cases of hypohidrotic ectodermal dysplasia caused by novel deletion mutations in the EDA gene.
Journal: The Journal of dermatology
Published: June 16, 2018
A case of mumps-related acute encephalopathy with biphasic seizures and late reduced diffusion.
Journal: Brain & development
Published: February 11, 2017
Evaluation of surgical treatment for intractable aspiration in neurologically impaired patients: our experience with 20 patients
Journal: No to hattatsu = Brain and development
Published: January 01, 2016
Mucolipidosis IV: A milder form with novel mutations and serial MRI findings.
Journal: Brain & development
Published: November 21, 2015
Protein-losing enteropathy as a rare complication of the ketogenic diet.
Journal: Pediatric neurology
Published: November 04, 2014
Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34.
Journal: Brain & development
Published: July 08, 2014
A novel PLP1 frameshift mutation causing a milder form of Pelizaeus-Merzbacher disease.
Journal: Brain & development
Published: April 16, 2014
Serum and CSF biomarkers in acute pediatric neurological disorders.
Journal: Brain & development
Published: February 28, 2013
Last Updated: 09/26/2026