Dysferlinopathy Latest Advances

Complement C5 Inhibitor Ameliorates a Case of Dysferlinopathy.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: January 13, 2026

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

Journal: Journal of neuromuscular diseases

Published: September 30, 2025

Pathomorphological characteristics of inflammatory and hereditary myopathies

Journal: Arkhiv patologii

Published: September 03, 2025

Boldo Restores Vascularization and Reduces Skeletal Muscle Inflammation in Symptomatic Mice with Dysferlinopathy.

Journal: International journal of molecular sciences

Published: August 14, 2025

Restoration of Dysferlin After Exon 32 Skipping in Patient Cells.

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

Infertility Due to a Novel Variant of a Balanced Y;1 Translocation: A Case Report.

Journal: Cureus

Published: July 05, 2025

Untangling Complexity in Dysferlinopathy With MRI Modeling of Disease Trajectory.

Journal: Neurology. Genetics

Published: June 11, 2025

Comprehensive Profiling of Annexins in Neuromuscular Disorders Reveals a Unique Signature in Dysferlinopathy.

Journal: European journal of neurology

Published: April 10, 2025

Cardiac MRI for early detection of subclinical cardiac dysfunction in dysferlinopathy.

Journal: Neuromuscular disorders : NMD

Published: April 05, 2025

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

Journal: Orphanet journal of rare diseases

Published: March 20, 2025

Antisense oligonucleotide-mediated exon 27 skipping restores dysferlin function in dysferlinopathy patient-derived muscle cells.

Journal: Molecular therapy. Nucleic acids

Published: February 24, 2025

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Complement C5 Inhibitor Ameliorates a Case of Dysferlinopathy.

Complement C5 Inhibitor Ameliorates a Case of Dysferlinopathy.

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

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

Pathomorphological characteristics of inflammatory and hereditary myopathies

Pathomorphological characteristics of inflammatory and hereditary myopathies

Boldo Restores Vascularization and Reduces Skeletal Muscle Inflammation in Symptomatic Mice with Dysferlinopathy.

Boldo Restores Vascularization and Reduces Skeletal Muscle Inflammation in Symptomatic Mice with Dysferlinopathy.

Restoration of Dysferlin After Exon 32 Skipping in Patient Cells.

Restoration of Dysferlin After Exon 32 Skipping in Patient Cells.

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

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

Infertility Due to a Novel Variant of a Balanced Y;1 Translocation: A Case Report.

Infertility Due to a Novel Variant of a Balanced Y;1 Translocation: A Case Report.

Untangling Complexity in Dysferlinopathy With MRI Modeling of Disease Trajectory.

Untangling Complexity in Dysferlinopathy With MRI Modeling of Disease Trajectory.

Comprehensive Profiling of Annexins in Neuromuscular Disorders Reveals a Unique Signature in Dysferlinopathy.

Comprehensive Profiling of Annexins in Neuromuscular Disorders Reveals a Unique Signature in Dysferlinopathy.

Cardiac MRI for early detection of subclinical cardiac dysfunction in dysferlinopathy.

Cardiac MRI for early detection of subclinical cardiac dysfunction in dysferlinopathy.

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

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

Antisense oligonucleotide-mediated exon 27 skipping restores dysferlin function in dysferlinopathy patient-derived muscle cells.

Antisense oligonucleotide-mediated exon 27 skipping restores dysferlin function in dysferlinopathy patient-derived muscle cells.