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Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findingsFabio Giannini, Stefania Battistini, Michelangelo Mancuso, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 18, 2021
A new mutation in DNM2 gene in a large Italian familyDiego Lopergolo, Silvia Bocci, Anna Maria Pinto, et al.
Therapeutic Advances in Musculoskeletal Disease|January 20, 2017
Histopathological findings in systemic sclerosis-related myopathy: fibrosis and microangiopathy with lack of cellular inflammationClaudio Corallo, Maurizio Cutolo, Nila Volpi, et al.
Journal of Neurology|May 28, 2004
Uncommon findings in idiopathic hypertrophic cranial pachymeningitisSimone Rossi, Fabio Giannini, Alfonso Cerase, et al.
Mediators of Inflammation|July 11, 2013
Antiangiogenic VEGF isoform in inflammatory myopathiesNila Volpi, Alessandra Pecorelli, Paola Lorenzoni, et al.
Neurology International|July 25, 2025
G-Protein-Coupled Estrogen Receptor (GPER) in Inflammatory MyopathiesDelia Righi, Diego Lopergolo, Nila Volpi, et al.
Journal of the Neurological Sciences|January 25, 2011
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) geneElena Cardaioli, Edoardo Malfatti, Paola Da Pozzo, et al.
Archives of Neurology|August 8, 2002
Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degenerationRaffaella Zannolli, Sid Gilman, Simone Rossi, et al.
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