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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 17, 2008
Cerebrovascular risk factors and MRI abnormalities in migraineRenata Rao, Anna Rosati, Paolo Liberini, et al.
Headache|November 23, 2006
Endothelial nitric oxide synthase (Glu298Asp) polymorphism is an independent risk factor for migraine with auraBarbara Borroni, Renata Rao, Paolo Liberini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 27, 2012
Reduction in retinal nerve fiber layer thickness in migraine patientsStefano Gipponi, Niccolò Scaroni, Elisabetta Venturelli, et al.
Pharmacology, Biochemistry, and Behavior|July 16, 2002
Spinal cord mGlu1a receptors: possible target for amyotrophic lateral sclerosis therapyAlessandra Valerio, Marina Ferrario, Marta Paterlini, et al.
The Journal of Headache and Pain|December 20, 2005
Functional serotonin 5-HTTLPR polymorphism is a risk factor for migraine with auraBarbara Borroni, Cristina Brambilla, Paolo Liberini, et al.
Neurology International|February 22, 2023
Migraine Disability Improvement during Treatment with Galcanezumab in Patients with Chronic and High Frequency Episodic MigraineFrancesca Schiano di Cola, Marco Bolchini, Salvatore Caratozzolo, et al.
Headache|February 24, 2006
Investigating the association between Notch3 polymorphism and migraineBarbara Borroni, Cristina Brambilla, Paolo Liberini, et al.
Frontiers in Pain Research (Lausanne, Switzerland)|November 25, 2022
Post COVID-19 vaccination headache: A clinical and epidemiological evaluationGiulia Ceccardi, Francesca Schiano di Cola, Marco Di Cesare, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 22, 2020
Diaphragmatic myoclonus due to SARS-CoV-2 infectionBarbara Borroni, Stefano Gazzina, Fedele Dono, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 29, 2006
Atypical phenotypes and clinical variability in a large Italian family with DYT1-primary torsion dystoniaMattia Gambarin, Enza Maria Valente, Paolo Liberini, et al.
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