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Last Updated: 10/31/2025
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Found 58 publications
Muscle MRI in a Rare Case of Limb-Girdle Muscular Dystrophy 1B.
Journal: Cureus
Published: October 26, 2024
Somatic and germinal mosaicism of a canonical splicing variant causing limb-girdle muscular dystrophy type 1B.
Journal: Journal of applied genetics
Published: September 13, 2024
The Influence of a Genetic Variant in CCDC78 on LMNA-Associated Skeletal Muscle Disease.
Journal: International journal of molecular sciences
Published: March 13, 2024
Characterization of cardiac involvement in children with LMNA-related muscular dystrophy.
Journal: Frontiers in cell and developmental biology
Published: January 12, 2023
Somatic and germinal mosaicism in a Han Chinese family with laminopathies.
Journal: European journal of human genetics : EJHG
Published: June 08, 2022
Functional Ability and Physical Activity in Hereditary Neuromuscular Diseases.
Journal: Journal of neuromuscular diseases
Published: February 18, 2022
A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort.
Journal: Journal of neuromuscular diseases
Published: October 04, 2021
Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.
Journal: International journal of molecular sciences
Published: October 22, 2020
Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy.
Journal: Orphanet journal of rare diseases
Published: February 18, 2020
Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients.
Journal: Journal of medical genetics
Published: November 01, 2019
Last Updated: 10/31/2025