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2. The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world setting

6. Essential components of an effective transition from paediatric to adult neurologist care for adolescents with Duchenne muscular dystrophy; a consensus derived using the Delphi methodology in Eastern Europe, Greece and Israel.

7. Phenotypic characteristics of F64L, I68L, I107V, and S77Y ATTRv genotypes from the Transthyretin Amyloidosis Outcomes Survey (THAOS)

10. Amino acid sequence homology of monoclonal serum free light chain dimers and tissue deposited light chains in AL amyloidosis: a pilot study.

11. Cross-species modeling of muscular dystrophy in Caenorhabditis elegans using patient-derived extracellular vesicles

12. Muscular dystrophy patients show low exercise‐induced blood flow in muscles with normal strength.

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