Last Updated: 09/26/2026
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Found 24 publications
Natural history of limb girdle muscular dystrophy R1 (LGMDR1): a GRASP consortium study.
Journal: Neuromuscular disorders : NMD
Published: December 10, 2025
General and Spine-Specific Sarcopenia in Adult Spinal Deformity: a Narrative Overview of Current Strengths and Limitations.
Journal: Global spine journal
Published: October 29, 2025
Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy.
Journal: The Journal of clinical investigation
Published: May 15, 2025
Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approaches.
Journal: Disease models & mechanisms
Published: November 06, 2024
Elevated VCP ATPase Activity Correlates With Disease Onset in Multisystem Proteinopathy-1.
Journal: Neurology. Genetics
Published: April 17, 2024
Genetic-Based Treatment Strategies for Muscular Dystrophy and Congenital Myopathies.
Journal: Continuum (Minneapolis, Minn.)
Published: December 20, 2022
DNAJB6 isoform specific knockdown: Therapeutic potential for limb girdle muscular dystrophy D1.
Journal: Molecular therapy. Nucleic acids
Published: November 17, 2022
LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials.
Journal: Annals of clinical and translational neurology
Published: November 07, 2022
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure.
Journal: Acta neuropathologica
Published: September 15, 2022
Clinical utility of anti-cytosolic 5'-nucleotidase 1A antibody in idiopathic inflammatory myopathies.
Journal: Annals of clinical and translational neurology
Published: September 21, 2020
Phenotypic diversity in an international Cure VCP Disease registry.
Journal: Orphanet journal of rare diseases
Published: June 24, 2020
Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy.
Journal: The Journal of clinical investigation
Published: January 06, 2020
Last Updated: 09/26/2026