Publications by authors named "F Taroni"
The article focuses on a careful description of literature on stylometry and on its potential use in forensic science. The state of the art of stylometry is summarized to illustrate the history and the scientific foundation of this discipline. However, the study conducted reveals that there are still some key unresolved aspects that require a response from the academic world.
View Article and Find Full Text PDFGenetic variants in gene, encoding for the glycyl tRNA synthetase 1, cause Charcot-Marie-Tooth disease, type 2D (CMT2D). Here we describe a 14-year-old boy affected by neuropathy with prominent weakness in the upper extremities carrying two missense variants in gene: the c.803C > T, p.
View Article and Find Full Text PDFArticle Synopsis
- Repeat expansions in the C9orf72 gene are a leading genetic cause of ALS and frontotemporal dementia, but understanding how this mutation causes neuron death is still unclear, complicating the search for effective therapies.
- Researchers analyzed data from over 41,000 ALS and healthy samples to identify potential treatments, discovering that acamprosate, a drug used for other conditions, might be repurposed for C9orf72-related diseases.
- Their findings demonstrated that acamprosate has neuroprotective properties in cell models and works similarly well as the current treatment, riluzole, showing the potential of using genomic data to find new drug applications.
Article Synopsis
- Researchers looked at children in Italy who were hospitalized for a urinary infection and checked their sodium (Na) and potassium (K) levels.
- They found that 23% of the kids had low sodium, while some had high potassium or both low sodium and high potassium.
- The study also discovered that specific levels in the blood and age were linked to these imbalances, with the most common issue being low sodium.