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Neurology|January 14, 2004
A novel mutation in SACS gene in a family from southern ItalyC Criscuolo, S Banfi, M Orio, et al.AJNR. American Journal of Neuroradiology|April 23, 2021
Unraveling Deep Gray Matter Atrophy and Iron and Myelin Changes in Multiple SclerosisG Pontillo, M Petracca, S Monti, et al.Journal of Medical Genetics|June 6, 2008
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonismC Piccoli, M Ripoli, G Quarato, et al.Minerva Ginecologica|November 6, 2014
A pharmacogenetic-driven approach for controlled ovarian hyperstimulation by FSH treatmentR Colognato, R Aiello, F Dulcetti, et al.European Journal of Neurology|August 14, 2018
Retinal vascular density in multiple sclerosis: a 1-year follow-upR Lanzillo, G Cennamo, M Moccia, et al.AJNR. American Journal of Neuroradiology|December 22, 2018
Determinants of Deep Gray Matter Atrophy in Multiple Sclerosis: A Multimodal MRI StudyG Pontillo, S Cocozza, R Lanzillo, et al.AJNR. American Journal of Neuroradiology|March 2, 2023
MR Imaging Signs of Gadolinium Retention Are Not Associated with Long-Term Motor and Cognitive Outcomes in Multiple SclerosisA Scaravilli, M Tranfa, G Pontillo, et al.Scientific Reports|March 14, 2019
Glatiramer Acetate modulates ion channels expression and calcium homeostasis in B cell of patients with relapsing-remitting multiple sclerosisC Criscuolo, A Cianflone, R Lanzillo, et al.Neurology|April 26, 2006
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic studyC Criscuolo, L Chessa, S Di Giandomenico, et al.Neurogenetics|December 6, 2003
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locusM Muglia, C Criscuolo, A Magariello, et al.Pageof 3