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Epileptic Disorders : International Epilepsy Journal with Videotape|March 20, 2012
Transient periodic lateralised epileptiform discharges (PLEDs) following internal carotid artery stentingDaniela Marino, Giampaolo Vatti, Alessandra Rufa, et al.Archives of Neurology|June 24, 2004
A novel NOTCH3 frameshift deletion and mitochondrial abnormalities in a patient with CADASILMaria Teresa Dotti, Nicola De Stefano, Silvia Bianchi, et al.Journal of the Neurological Sciences|March 22, 2017
SPG2 mimicking multiple sclerosis in a family identified using next generation sequencingAnna Rubegni, Carla Battisti, Alessandra Tessa, et al.Biomolecules|September 27, 2025
The First Heterozygous TWNK Nonsense Mutation Associated with Progressive External Ophthalmoplegia: Evidence for a New Piece in the Puzzle of Mitochondrial DiseasesDiego Lopergolo, Gianna Berti, Gian Nicola Gallus, et al.Journal of the Neurological Sciences|August 17, 2010
A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional featuresEdoardo Malfatti, Elena Cardaioli, Carla Battisti, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 27, 2013
Homozygosity and severity of phenotypic presentation in a CADASIL familyClaudia Vinciguerra, Alessandra Rufa, Silvia Bianchi, et al.Journal of the Neurological Sciences|August 29, 2012
Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutationElena Cardaioli, Edoardo Malfatti, Carla Battisti, et al.Brain & Development|October 16, 2016
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrumSalvatore Grosso, Maria Alessandra Carluccio, Elena Cardaioli, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 8, 2015
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance?Paola Da Pozzo, Anna Rubegni, Alessandra Rufa, et al.Journal of the Neurological Sciences|June 5, 2004
Antibodies to dorsal root ganglia and olfactory cells in a patient with chronic sensory neuropathy and anosmiaSimona Gambelli, Federica Ginanneschi, Alessandro Malandrini, et al.Pageof 7