Miyoshi Myopathy Latest Advances

Find the Latest Research About Miyoshi Myopathy

Last Updated: 04/28/2026

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Found 262 publications

Dysferlinopathies: phenotypic study of a Moroccan series of 28 cases.

Dysferlinopathies: phenotypic study of a Moroccan series of 28 cases.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: January 13, 2026

DYSF gene variant spectrum in Arab populations across eight countries: A systematic review.

DYSF gene variant spectrum in Arab populations across eight countries: A systematic review.

Journal: Biomolecules & biomedicine
Published: October 25, 2025

An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.

An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.

Journal: Journal of neuromuscular diseases
Published: September 30, 2025

Tips to Design Effective Splice-Switching Antisense Oligonucleotides for Exon Skipping and Exon Inclusion.

Tips to Design Effective Splice-Switching Antisense Oligonucleotides for Exon Skipping and Exon Inclusion.

Journal: Methods in molecular biology (Clifton, N.J.)
Published: July 28, 2025

An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases.

An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases.

Journal: Methods in molecular biology (Clifton, N.J.)
Published: July 28, 2025

A Late-Onset Presentation of Miyoshi Myopathy: A Case Report.

A Late-Onset Presentation of Miyoshi Myopathy: A Case Report.

Journal: Cureus
Published: July 10, 2025

In Vitro Correction of Point Mutations in the DYSF Gene Using Prime Editing.

In Vitro Correction of Point Mutations in the DYSF Gene Using Prime Editing.

Journal: International journal of molecular sciences
Published: April 28, 2025

Dysferlinopathy as cause of long-term hyperCKemia with preserved strength.

Dysferlinopathy as cause of long-term hyperCKemia with preserved strength.

Journal: Orphanet journal of rare diseases
Published: March 20, 2025

Whole Exome Sequencing Identified a Stop-Gained Mutation in DYSF Gene Associated With Dysferlinopathy in an Iranian Family.

Whole Exome Sequencing Identified a Stop-Gained Mutation in DYSF Gene Associated With Dysferlinopathy in an Iranian Family.

Journal: International journal of genomics
Published: January 16, 2025

Clinical Presentation, Diagnosis, and Genetic Insights of Miyoshi Myopathy: A Case Report and Literature Review.

Clinical Presentation, Diagnosis, and Genetic Insights of Miyoshi Myopathy: A Case Report and Literature Review.

Journal: Cureus
Published: September 07, 2024

Limb Girdle Muscular Dystrophy Type 2B (LGMD2B): Diagnosis and Therapeutic Possibilities.

Limb Girdle Muscular Dystrophy Type 2B (LGMD2B): Diagnosis and Therapeutic Possibilities.

Journal: International journal of molecular sciences
Published: April 18, 2024

Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy.

Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy.

Journal: Neuromuscular disorders : NMD
Published: March 26, 2024
Showing 1-12 of 262

Last Updated: 04/28/2026