Nobuyuki Eura

Nara-shi, Japan

Last Updated: 09/26/2026

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Found 45 publications

Case Report: Anti-LGI1 encephalitis during FcRn inhibition with efgartigimod for myasthenia gravis: implications for the limitations of IgG recycling blockade.

Case Report: Anti-LGI1 encephalitis during FcRn inhibition with efgartigimod for myasthenia gravis: implications for the limitations of IgG recycling blockade.

Journal: Frontiers in immunology

Published: April 13, 2026

A Rare Association of Anti-SRP Antibody-Positive Immune-Mediated Necrotizing Myopathy and Sjögren Disease: Two Case Reports.

A Rare Association of Anti-SRP Antibody-Positive Immune-Mediated Necrotizing Myopathy and Sjögren Disease: Two Case Reports.

Journal: Muscle & nerve

Published: January 24, 2026

Medically Managed Dropped Head Syndrome: Outcomes in Isolated Neck Extensor Myopathy and Primary Hyperparathyroidism-related Myopathy.

Medically Managed Dropped Head Syndrome: Outcomes in Isolated Neck Extensor Myopathy and Primary Hyperparathyroidism-related Myopathy.

Journal: Internal medicine (Tokyo, Japan)

Published: November 19, 2025

Myopathies: Radiologist's Essential Tips for Clinical, Pathologic, and Imaging Findings.

Myopathies: Radiologist's Essential Tips for Clinical, Pathologic, and Imaging Findings.

Journal: Radiographics : a review publication of the Radiological Society of North America, Inc

Published: October 09, 2025

MBNL depletion drives stem cell fusion and immature myonuclear states in myotonic dystrophy type 1.

MBNL depletion drives stem cell fusion and immature myonuclear states in myotonic dystrophy type 1.

Journal: Nature communications

Published: August 06, 2025

Pathogenic CGG expansions in oculopharyngodistal myopathy exhibit distinct characteristics of each causative gene on the flanking sequences as well as methylation status.

Pathogenic CGG expansions in oculopharyngodistal myopathy exhibit distinct characteristics of each causative gene on the flanking sequences as well as methylation status.

Journal: Genome medicine

Published: July 15, 2025

A case of asymptomatic hyperCKemia for 40 years leading to a diagnosis of treatable immune-mediated necrotizing myopathy.

A case of asymptomatic hyperCKemia for 40 years leading to a diagnosis of treatable immune-mediated necrotizing myopathy.

Journal: Neuromuscular disorders : NMD

Published: June 30, 2025

SNUPN variants cause spinocerebellar atrophy by disrupting global splicing in cerebellar Purkinje cells.

SNUPN variants cause spinocerebellar atrophy by disrupting global splicing in cerebellar Purkinje cells.

Journal: Brain : a journal of neurology

Published: April 04, 2025

GGC repeat expansions within new open reading frames are translated into toxic polyglycine proteins in oculopharyngodistal myopathy.

GGC repeat expansions within new open reading frames are translated into toxic polyglycine proteins in oculopharyngodistal myopathy.

Journal: Nature genetics

Published: February 28, 2025

Comparative Analysis of CRISPR/Cas9-targeted Nanopore Sequencing Approaches in Repeat Expansion Disorders.

Comparative Analysis of CRISPR/Cas9-targeted Nanopore Sequencing Approaches in Repeat Expansion Disorders.

Journal: Genomics, proteomics & bioinformatics

Published: July 30, 2024

Response to: Calpainopathy Can Manifest Itself in Not Only Skeletal Muscle but Also the Brain and Myocardium.

Response to: Calpainopathy Can Manifest Itself in Not Only Skeletal Muscle but Also the Brain and Myocardium.

Journal: Internal medicine (Tokyo, Japan)

Published: May 29, 2024

X-linked Myotubular Myopathy Manifesting Carrier with Central and Peripheral Nervous System Involvement.

X-linked Myotubular Myopathy Manifesting Carrier with Central and Peripheral Nervous System Involvement.

Journal: Internal medicine (Tokyo, Japan)

Published: April 17, 2024

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Last Updated: 09/26/2026