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2. A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia. Issue 9 (1st July 2015)

3. Aging‐associated genes and let‐7 microRNAs: a contribution to myogenic program dysregulation in oculopharyngeal muscular dystrophy. Issue 6 (12th March 2019)

4. Biobank of Cells, Tissues and DNA from Patients with Neuromuscular Diseases: An Indispensable link between Clinical Centers and the Scientific Community. (13th February 2017)

5. Botulinum toxin type A affects the transcriptome of cell cultures derived from muscle biopsies of controls and spastic patients. (August 2018)

6. Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1. Issue 12 (17th October 2014)

7. Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patients. Issue 2 (28th January 2020)

8. Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by β sarcoglycan mutations. Issue 2 (1st February 2000)

9. Expanding the central nervous system disease spectrum associated with FLNC mutation. Issue 5 (20th February 2019)

10. Genetic defects are common in myopathies with tubular aggregates. Issue 1 (15th December 2021)