Satoshi Ishihara

Okinawa, Japan

Last Updated: 09/26/2026

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Found 13 publications

Multicenter, randomized, double-blind, placebo-controlled phase 3 study of mogamulizumab with open-label extension study in a minimum number of patients with human T-cell leukemia virus type-1-associated myelopathy.

Multicenter, randomized, double-blind, placebo-controlled phase 3 study of mogamulizumab with open-label extension study in a minimum number of patients with human T-cell leukemia virus type-1-associated myelopathy.

Journal: Journal of neurology

Published: November 07, 2023

Power spectral analysis of heart rate variability is useful as a screening tool for detecting sympathetic and parasympathetic nervous dysfunctions in Parkinson's disease.

Power spectral analysis of heart rate variability is useful as a screening tool for detecting sympathetic and parasympathetic nervous dysfunctions in Parkinson's disease.

Journal: BMC neurology

Published: April 27, 2022

Efficacy of Corticosteroid Therapy for HTLV-1-Associated Myelopathy: A Randomized Controlled Trial (HAMLET-P).

Efficacy of Corticosteroid Therapy for HTLV-1-Associated Myelopathy: A Randomized Controlled Trial (HAMLET-P).

Journal: Viruses

Published: December 06, 2021

Clinical features of inherited neuropathy with BSCL2 mutations in Japan.

Clinical features of inherited neuropathy with BSCL2 mutations in Japan.

Journal: Journal of the peripheral nervous system : JPNS

Published: December 16, 2019

Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan.

Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan.

Journal: Journal of the peripheral nervous system : JPNS

Published: December 06, 2017

Complimentary use of needle electromyography and ultrasonography of tongue is effective for early detection of abnormality in 20 patients with amyotrophic lateral sclerosis

Complimentary use of needle electromyography and ultrasonography of tongue is effective for early detection of abnormality in 20 patients with amyotrophic lateral sclerosis

Journal: Rinsho shinkeigaku = Clinical neurology

Published: October 27, 2017

Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.

Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.

Journal: Brain : a journal of neurology

Published: August 31, 2017

The Sequential Ultrasonographic, Electrophysiological and MRI Findings in a Patient with the Pharyngeal-cervical-brachial Variant of Guillain-Barré Syndrome from the Acute Phase to the Chronic Phase.

The Sequential Ultrasonographic, Electrophysiological and MRI Findings in a Patient with the Pharyngeal-cervical-brachial Variant of Guillain-Barré Syndrome from the Acute Phase to the Chronic Phase.

Journal: Internal medicine (Tokyo, Japan)

Published: May 16, 2017

Clinical manifestations of 5 patients with idiopathic paroxysmal kinesigenic choreoathetosis

Clinical manifestations of 5 patients with idiopathic paroxysmal kinesigenic choreoathetosis

Journal: Rinsho shinkeigaku = Clinical neurology

Published: February 19, 2016

Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2.

Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2.

Journal: Annals of neurology

Published: October 13, 2015

Dolichoectatic vertebrobasilar dissecting aneurysm originating from atherosclerosis: an autopsy case.

Dolichoectatic vertebrobasilar dissecting aneurysm originating from atherosclerosis: an autopsy case.

Journal: Internal medicine (Tokyo, Japan)

Published: August 20, 2013

Increased expression of OX40 is associated with progressive disease in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis.

Increased expression of OX40 is associated with progressive disease in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis.

Journal: Retrovirology

Published: December 04, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026