Yusuke Sakiyama

Kagoshima, Japan

Last Updated: 09/26/2026

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Found 51 publications

Biallelic SIGMAR1 variants in early-onset distal hereditary motor neuropathy: A Japanese case series.

Biallelic SIGMAR1 variants in early-onset distal hereditary motor neuropathy: A Japanese case series.

Journal: Journal of neuromuscular diseases

Published: August 25, 2026

Metagenomic analysis for central nervous system infections: clinical utility and future directions

Metagenomic analysis for central nervous system infections: clinical utility and future directions

Journal: Rinsho shinkeigaku = Clinical neurology

Published: June 17, 2026

Varicella-Zoster Virus Infections of the Central Nervous System

Varicella-Zoster Virus Infections of the Central Nervous System

Journal: Brain and nerve = Shinkei kenkyu no shinpo

Published: May 19, 2026

Longitudinal motor function and biomarker correlates in treated adult spinal muscular atrophy: a single-center cohort study.

Longitudinal motor function and biomarker correlates in treated adult spinal muscular atrophy: a single-center cohort study.

Journal: Frontiers in neurology

Published: May 01, 2026

Functional and Epigenomic Consequences of DNMT1 Variants in Inherited Neurological Disorders.

Functional and Epigenomic Consequences of DNMT1 Variants in Inherited Neurological Disorders.

Journal: International journal of molecular sciences

Published: November 23, 2025

HTLV-1-Specific CTL Accumulation in CSF Contributes to Neuroinflammation in HTLV-1-Associated Myelopathy.

HTLV-1-Specific CTL Accumulation in CSF Contributes to Neuroinflammation in HTLV-1-Associated Myelopathy.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: November 03, 2025

Arginine ameliorates motor and survival deficits in MFN2-Deficient Drosophila models.

Arginine ameliorates motor and survival deficits in MFN2-Deficient Drosophila models.

Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics

Published: September 10, 2025

Respiratory complex I deficiency caused by a novel multi-exonic PUS1 deletion.

Respiratory complex I deficiency caused by a novel multi-exonic PUS1 deletion.

Journal: Journal of human genetics

Published: September 08, 2025

INF2-Related Charcot-Marie-Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights.

INF2-Related Charcot-Marie-Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights.

Journal: Annals of clinical and translational neurology

Published: August 06, 2025

Tibial to ulnar nerve amplitude ratio as a marker of length-dependent neuropathy.

Tibial to ulnar nerve amplitude ratio as a marker of length-dependent neuropathy.

Journal: Clinical neurophysiology practice

Published: August 01, 2025

Biallelic variants in FAT3 cause axonal neuropathy with multisystem neurodevelopmental features.

Biallelic variants in FAT3 cause axonal neuropathy with multisystem neurodevelopmental features.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 26, 2025

Nationwide Characterization of MFN2-Related CMT in 176 Japanese Patients: Clinical and Genetic Insights.

Nationwide Characterization of MFN2-Related CMT in 176 Japanese Patients: Clinical and Genetic Insights.

Journal: Annals of clinical and translational neurology

Published: July 19, 2025

Showing 1-12 of 51

Last Updated: 09/26/2026