Session IV-b: Biology and Physiopathology of Genetic Neuromuscular Diseases

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• Abstract 029 | Adulthood transition age in dystrophinopathies: a management model for integrated care delivery in Tuscany region

  Giulia Ricci ¹, Francesca Torri ¹, Sara Loprieno ¹, Mariaconcetta Rende ¹, Aruzhan Nugumanova ¹, Michele Sacchini ², Chiara Ticci ², Guja Astrea ³, Bianca Buchignani ³, Elena Procopio ², Roberta Battini ³, Gabriele Siciliano ¹ | ¹Department of Clinical and Experimental Medicine, University of Pisa, Italy; ²Metabolic and Muscular Diseases Unit, Meyer Children's Hospital IRCCS, Italy; ³Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, IRCCS Stella Maris Foundation, Calambrone Pisa, Italy.

  Giulia Ricci

  DOI https://doi.org/10.4081/ejtm.2026.15028

  • 262 abstract views
  • 148 PDF

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• Abstract 030 | Expression of the ERG1A potassium channel affects nanoscale membrane characteristics of cultured skeletal muscle cells

  Amber L. Pond ¹, Annie Yojaira Vargas Lizarazo ², Judith K. Davie ¹, Punit Kohli ² | ¹Department of Basic Medical Sciences, School of Medicine, Southern Illinois University; ²School of Chemical and Biomolecular Sciences, Southern Illinois University Carbondale, Illinois, USA.

  Amber L. Pond

  DOI https://doi.org/10.4081/ejtm.2026.15029

  • 231 abstract views
  • 154 PDF

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• Abstract 031 | Lecture: the wonderful machine

  Stefano Schiaffino | Veneto Institute of Molecular Medicine - VIMM, Padua, Italy Veneto Institute of Molecular Medicine - VIMM, Padua, Italy.

  Stefano Schiaffino

  DOI https://doi.org/10.4081/ejtm.2026.15030

  • 238 abstract views
  • 123 PDF

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• Abstract 028 | Modelling satellite cell dysfunction to understand pathogenesis of neuromuscular disorders

  Massimo Ganassi | Genetic Therapy Accelerator Centre, Queen Square Institute of Neurology, University College London, London, UK.

  Massimo Ganassi

  DOI https://doi.org/10.4081/ejtm.2026.15027

  • 265 abstract views
  • 153 PDF

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