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Journal of Neuromuscular Diseases|May 6, 2026
Clinical and pathological findings in two Italian siblings of Romani ancestry with charcot-marie-tooth type 4D and review of the current literatureElena Abati, Carola Rita Ferrari Aggradi, Stefania Magri, et al.
Blood|March 1, 1988
Sardinian G gamma-HPFH: a T----C substitution in a conserved "octamer" sequence in the G gamma-globin promoterS Ottolenghi, S Nicolis, R Taramelli, et al.
International Journal of Molecular Sciences|January 27, 2017
Polymorphisms of Dopamine Receptor Genes and Risk of L-Dopa-Induced Dyskinesia in Parkinson's DiseaseCristoforo Comi, Marco Ferrari, Franca Marino, et al.
Neurobiology of Aging|June 28, 2014
Disrupted brain connectome in semantic variant of primary progressive aphasiaFederica Agosta, Sebastiano Galantucci, Paola Valsasina, et al.
Frontiers in Neurology|June 1, 2022
Newly Diagnosed Hepatic Encephalopathy Presenting as Non-convulsive Status Epilepticus: A Case Report and Literature ReviewMarco Olivero, Delia Gagliardi, Gianluca Costamagna, et al.
Antiviral Therapy|April 29, 2022
Rilpivirine plus cobicistat-boosted darunavir as alternative to standard three-drug therapy in HIV-infected, virologically suppressed subjects: Final results of the PROBE 2 trialFranco Maggiolo, Nicola Gianotti, Laura Comi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 3, 2010
Comparative study of mitoxantrone efficacy profile in patients with relapsing-remitting and secondary progressive multiple sclerosisFederica Esposito, Marta Radaelli, Vittorio Martinelli, et al.
Radiology|March 11, 2016
Brain MR Imaging in Patients with Lower Motor Neuron-Predominant DiseaseEdoardo G Spinelli, Federica Agosta, Pilar M Ferraro, et al.
Annals of Neurology|November 25, 2004
High tumor necrosis factor-alpha [corrected] levels in cerebrospinal fluid of cobalamin-deficient patientsGiuseppe Scalabrino, Marinella Carpo, Fabrizia Bamonti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 19, 2013
White matter abnormalities in Parkinson's disease patients with glucocerebrosidase gene mutationsFederica Agosta, Vladimir S Kostic, Kristina Davidovic, et al.
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