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  1. Article

    Open Access

    Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

    Sarah Opie-Martin, Alfredo Iacoangeli, Simon D. Topp in Nature Communications (2024)

  2. Article

    Open Access

    The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

    Superoxide dismutase (SOD1) gene variants may cause amyotrophic lateral sclerosis, some of which are associated with a distinct phenotype. Most studies assess limited variants or sample sizes. In this internation...

    Sarah Opie-Martin, Alfredo Iacoangeli, Simon D. Topp in Nature Communications (2022)

  3. Article

    Open Access

    Author Correction: A HML6 endogenous retrovirus on chromosome 3 is upregulated in amyotrophic lateral sclerosis motor cortex

    Ashley R. Jones, Alfredo Iacoangeli, Brett N. Adey, Harry Bowles in Scientific Reports (2022)

  4. Article

    Open Access

    Amyotrophic lateral sclerosis and cerebellum

    Amyotrophic lateral sclerosis (ALS) is a devastating, heterogeneous neurodegenerative neuromuscular disease that leads to a fatal outcome within 2–5 years, and yet, a precise nature of the association between ...

    Renata Kabiljo, Alfredo Iacoangeli, Ammar Al-Chalabi in Scientific Reports (2022)

  5. Article

    Open Access

    A HML6 endogenous retrovirus on chromosome 3 is upregulated in amyotrophic lateral sclerosis motor cortex

    There is increasing evidence that endogenous retroviruses (ERVs) play a significant role in central nervous system diseases, including amyotrophic lateral sclerosis (ALS). Studies of ALS have consistently iden...

    Ashley R. Jones, Alfredo Iacoangeli, Brett N. Adey, Harry Bowles in Scientific Reports (2021)