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Scientific Reports|June 25, 2026
Model architecture dominates nutritional estimation accuracy in vision-language systemsLuca Vedovelli, Sofia Pugnaloni, Corrado Lanera, et al.
Journal of the Neurological Sciences|December 10, 2023
Troponin T in spinal and bulbar muscular atrophy (SBMA)Giulia Musso, Lorenzo Blasi, Monica Maria Mion, et al.
Journal of Neurology|November 16, 2022
Italian version of the Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS): validation and longitudinal performanceAndrea Fortuna, Daniele Sabbatini, Annachiara Frigo, et al.
Scientific Reports|October 12, 2023
The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA)Lorenzo Blasi, Daniele Sabbatini, Andrea Fortuna, et al.
European Journal of Neurology|February 7, 2025
MEPs and MRI Motor Band Sign as Potential Complementary Markers of Upper Motor Neuron Involvement in Amyotrophic Lateral SclerosisFrancesca Calvi, Andrea Fortuna, Luca Bello, et al.
International Journal of Legal Medicine|September 7, 2021
Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome PanelChristian Faccinetto, Daniele Sabbatini, Patrizia Serventi, et al.
Annals of Clinical and Translational Neurology|July 15, 2021
Evaluation of peripherin in biofluids of patients with motor neuron diseasesDaniele Sabbatini, Flavia Raggi, Susanna Ruggero, et al.
European Journal of Neurology|March 17, 2026
Wernicke Encephalopathy Complicating a Distinctive POLG Phenotype With MNGIE-Like FeaturesGiuliana Capece, Luca Caumo, Sara Volta, et al.
Neurology. Genetics|July 30, 2025
Longitudinal Changes of Motor Function in Becker Muscular DystrophyLuca Bello, Pietro Riguzzi, Giuliana Capece, et al.
Journal of Clinical Pharmacology|April 29, 2024
Assessing Pharmacogenomic loci Associated with the Pharmacokinetics of Vamorolone in Boys with Duchenne Muscular DystrophyXiaonan Li, Daniele Sabbatini, Elena Pegoraro, et al.
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