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Last Updated: 10/31/2025
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Found 57 publications
Evaluation of cardiomyopathy with two-dimensional speckle tracking echocardiography in limb-girdle muscular dystrophy type 2A and 2B.
Journal: Journal of clinical ultrasound : JCU
Published: June 23, 2022
Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India.
Journal: Global medical genetics
Published: July 07, 2021
Variants of CAPN3 cause limb-girdle muscular dystrophy type 2A in two Chinese families.
Journal: Experimental and therapeutic medicine
Published: February 17, 2020
Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia.
Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia.
Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: December 03, 2019
Titin splicing regulates cardiotoxicity associated with calpain 3 gene therapy for limb-girdle muscular dystrophy type 2A.
Journal: Science translational medicine
Published: January 30, 2019
Coincidence of hereditary motor and sensory neuropathy type 1A and limb girdle muscular dystrophy type 2A
Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Published: December 27, 2018
Severe limb-girdle muscular dystrophy 2A in two young siblings from Guinea-Bissau associated with a novel null homozygous mutation in CAPN3 gene.
Journal: Neuromuscular disorders : NMD
Published: September 01, 2018
Limb-girdle Muscular Dystrophy Type 2A with Muscular Eosinophilic Infiltration in a Chinese Patient.
Limb-girdle Muscular Dystrophy Type 2A with Muscular Eosinophilic Infiltration in a Chinese Patient.
Journal: Chinese medical journal
Published: August 22, 2018
Fatty infiltration evaluation and selective pattern characterization of lower limbs in limb-girdle muscular dystrophy type 2A by muscle magnetic resonance imaging.
Journal: Muscle & nerve
Published: October 16, 2017
Last Updated: 10/31/2025