Jesica M. Escudero-Exposito
Barcelona, CT, Spain
Last Updated: 09/26/2026
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Found 10 publications
IMU-based workspace area as a promising complementary tool to assess upper limb function in Neuromuscular diseases: A one-year follow-up.
Journal: Journal of neuromuscular diseases
Published: July 06, 2026
Real-world data on spinal muscular atrophy in Spain: Insights from over 500 individuals in the CuidAME project.
Journal: Journal of neuromuscular diseases
Published: July 29, 2025
Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot-Marie-Tooth Disease.
Journal: Annals of neurology
Published: April 01, 2025
Fetal Akinesia/Hypokinesia and Arthrogryposis of Neuromuscular Origin: Etiologic Groups, Genetics, and Phenotypic Spectrum.
Journal: Annals of clinical and translational neurology
Published: February 24, 2025
Correction: Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases.
Journal: European journal of human genetics : EJHG
Published: December 10, 2024
MYL1-Related Congenital Myopathy: Clinical, Genetic and Pathological Insights.
Journal: Neuropathology and applied neurobiology
Published: November 02, 2024
Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases.
Journal: European journal of human genetics : EJHG
Published: June 05, 2024
Full-Length SMN Transcript in Extracellular Vesicles as Biomarker in Individuals with Spinal Muscular Atrophy Type 2 Treated with Nusinersen.
Journal: Journal of neuromuscular diseases
Published: April 11, 2023
Pathological Features in Paediatric Patients with TK2 Deficiency.
Journal: International journal of molecular sciences
Published: August 12, 2022
Longitudinal Study of Three microRNAs in Duchenne Muscular Dystrophy and Becker Muscular Dystrophy.
Journal: Frontiers in neurology
Published: January 28, 2020
Showing 1-10 of 10
Last Updated: 09/26/2026