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Clinical Neurology and Neurosurgery|June 22, 2024
Tango classes in people with Multiple Sclerosis (PwMS): Impact on motor and non-motor functionsAssunta Trinchillo, Daniele Caliendo, Valerio Nicolella, et al.Journal of Neurology|March 3, 2005
The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathyValentina Scarano, Pietro Mancini, Chiara Criscuolo, et al.Human Molecular Genetics|August 14, 2003
DNA damage induced by polyglutamine-expanded proteinsPaola Giuliano, Tiziana De Cristofaro, Adelina Affaitati, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 16, 2006
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonismChiara Criscuolo, Giampiero Volpe, Anna De Rosa, et al.Neurogenetics|May 13, 2014
PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian familySimone Olgiati, Anna De Rosa, Marialuisa Quadri, et al.Journal of Neurology|November 16, 2007
Nigrostriatal involvement in ataxia with oculomotor apraxia type 1Elena Salvatore, Andrea Varrone, Chiara Criscuolo, et al.Environmental Microbiome|April 4, 2026
Prosystemin-derived signals: bridging leaf microbiome dynamics and defense activationValeria Castaldi, Wisnu Adi Wicaksono, Martina Chiara Criscuolo, et al.Orphanet Journal of Rare Diseases|April 6, 2023
Chenodeoxycholic acid rescues axonal degeneration in induced pluripotent stem cell-derived neurons from spastic paraplegia type 5 and cerebrotendinous xanthomatosis patientsYongchao Mou, Ghata Nandi, Sukhada Mukte, et al.Journal of Clinical Medicine|December 24, 2021
Retinal and Choriocapillary Vascular Changes in Early Stages of Multiple Sclerosis: A Prospective StudyDaniela Montorio, Roberta Lanzillo, Antonio Carotenuto, et al.Journal of Neuroimmunology|June 12, 2017
CD4/CD8 ratio during natalizumab treatment in multiple sclerosis patientsAntonio Carotenuto, Giulia Scalia, Francesco Ausiello, et al.Pageof 8