Hikaru Sakamoto
Sakai, Japan
Last Updated: 09/26/2026
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Found 16 publications
Pathological Findings in Male Patients With Anti-N-methyl-d-Aspartate Receptor Encephalitis.
Journal: Journal of neuropathology and experimental neurology
Published: July 09, 2019
Unexpectedly mild phenotype in an ataxic family with a two-base deletion in the APTX gene.
Journal: Journal of the neurological sciences
Published: December 03, 2016
Histopathological features of a patient with Charcot-Marie-Tooth disease type 2U/AD-CMTax-MARS.
Journal: Journal of the peripheral nervous system : JPNS
Published: August 19, 2016
Progression of Dysphagia in Spinocerebellar Ataxia Type 6.
Journal: Dysphagia
Published: August 17, 2016
The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan.
Journal: PloS one
Published: June 16, 2015
Differential Progression of Dysphagia in Heredity and Sporadic Ataxias Involving Multiple Systems.
Journal: European neurology
Published: May 18, 2015
Rotigotine Transdermal Patch Improves Swallowing in Dysphagic Patients with Parkinson's Disease.
Journal: Dysphagia
Published: March 17, 2015
Eyelid tremor in a patient with anti-caspr2 antibody-related encephalitis.
Journal: Case reports in neurology
Published: October 10, 2014
VCP gene analyses in Japanese patients with sporadic amyotrophic lateral sclerosis identify a new mutation.
Journal: Neurobiology of aging
Published: September 15, 2014
Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: March 12, 2014
A case of severe ganciclovir-induced encephalopathy.
Journal: Case reports in neurology
Published: January 10, 2014
A case of anti-N-methyl-d-aspartate receptor encephalitis with multiple sclerosis-like demyelinated lesions.
Journal: Multiple sclerosis and related disorders
Published: May 21, 2013
Last Updated: 09/26/2026