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Last Updated: 10/31/2025
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Found 260 publications
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.
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.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: July 28, 2025
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.
Journal: International journal of molecular sciences
Published: April 28, 2025
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.
Journal: International journal of genomics
Published: January 16, 2025
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.
Journal: Neuromuscular disorders : NMD
Published: March 26, 2024
Last Updated: 10/31/2025