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Journal of Cellular and Molecular Medicine|February 20, 2021
Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross-sectional studyDelia Gagliardi, Irene Faravelli, Megi Meneri, et al.
CEN Case Reports|December 14, 2017
Exertional rhabdomyolysis leading to acute kidney injury: when genetic defects are diagnosed in adult lifeDavid Cucchiari, Irene Colombo, Ottavia Amato, et al.
Plos One|November 13, 2012
Caprylic triglyceride as a novel therapeutic approach to effectively improve the performance and attenuate the symptoms due to the motor neuron loss in ALS diseaseWei Zhao, Merina Varghese, Prashant Vempati, et al.
Human Molecular Genetics|September 6, 2013
Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Biomedicines|May 27, 2023
Identification of Novel Biomarkers of Spinal Muscular Atrophy and Therapeutic Response by Proteomic and Metabolomic Profiling of Human Biological Fluid SamplesMegi Meneri, Elena Abati, Delia Gagliardi, et al.
Medicine|October 30, 2020
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literatureGianluca Costamagna, Megi Meneri, Elena Abati, et al.
Frontiers in Neurology|August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisRoberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Frontiers in Neurology|September 24, 2021
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort StudyDelia Gagliardi, Irene Faravelli, Manuel Alfredo Podestà, et al.
Frontiers in Neurology|August 18, 2018
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureDelia Gagliardi, Irene Faravelli, Luisa Villa, et al.
BMC Neurology|December 29, 2018
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eyeEleonora Mauri, Robertino Dilena, Antonio Boccazzi, et al.
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