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Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2002
Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD geneSian D Spacey, Enza-Maria Valente, Gurusidheshwar M Wali, et al.Journal of Medical Genetics|September 11, 2025
Further evidence of <i>RNU4ATAC</i> variants causing Joubert syndrome with skeletal involvementFulvio D'Abrusco, Simone Gana, Enrico Alfei, et al.Revista Da Sociedade Brasileira De Medicina Tropical|April 22, 2021
Long-Term Persistence of Serum-Specific Anti-Chikungunya IgM Antibody - A Case Series of Brazilian PatientsDenise Maria do Nascimento Costa, Maria Rosângela Cunha Duarte Coêlho, Pedro Alves da Cruz Gouveia, et al.Journal of Fungi (Basel, Switzerland)|April 26, 2024
Potential Activity of Micafungin and Amphotericin B Co-Encapsulated in Nanoemulsion against Systemic <i>Candida auris</i> Infection in a Mice ModelGabriel Davi Marena, Gabriela Corrêa Carvalho, Alba Ruiz-Gaitán, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 30, 2011
The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in childrenAlessandra Terracciano, Florence Renaldo, Ginevra Zanni, et al.NPJ Parkinson'S Disease|October 25, 2024
CSF d18:1 sphingolipid species in Parkinson disease and dementia with Lewy bodies with and without GBA1 variantsStefanie Lerche, Isabel Wurster, Enza Maria Valente, et al.Annals of Clinical and Translational Neurology|January 29, 2026
Clustering Algorithm Reveals Dopamine-Motor Mismatch in Cognitively Preserved Parkinson's DiseaseRachele Malito, Chiara Meneghini, Alice Galli, et al.Neurogenetics|January 1, 2013
Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotypeCarlo C Quattrocchi, Ginevra Zanni, Antonio Napolitano, et al.Diagnostics (Basel, Switzerland)|June 2, 2021
Diagnostic Yield and Cost-Effectiveness of "Dynamic" Exome Analysis in Epilepsy with Neurodevelopmental Disorders: A Tertiary-Center Experience in Northern ItalyCostanza Varesio, Simone Gana, Alessia Asaro, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2003
Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneityEnza-Maria Valente, Anjum Misbahuddin, Francesco Brancati, et al.Pageof 36