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Annals of Clinical and Translational Neurology|November 22, 2017
Multigeneration family with dominant SPG30 hereditary spastic paraplegiaRicardo H Roda, Alice B Schindler, Craig BlackstoneAnnals of Clinical and Translational Neurology|May 12, 2017
De novo REEP2 missense mutation in pure hereditary spastic paraplegiaRicardo H Roda, Alice B Schindler, Craig BlackstoneThe Journal of Clinical Investigation|April 1, 2026
Genetic analysis of neurodegenerative diseasesMaurizio Grassano, Alice B Schindler, Bryan J Traynor, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 13, 2014
Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damageRicardo H Roda, Carlo Rinaldi, Rajat Singh, et al.Annals of Clinical and Translational Neurology|September 9, 2016
Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding siteRicardo H Roda, Edmond J FitzGibbon, Houda Boucekkine, et al.Case Reports in Neurology|October 3, 2017
TUBB2B Mutation in an Adult Patient with Myoclonus-DystoniaJoshua T Geiger, Alice B Schindler, Cornelis Blauwendraat, et al.Annals of Clinical and Translational Neurology|January 10, 2015
Laing distal myopathy pathologically resembling inclusion body myositisRicardo H Roda, Alice B Schindler, Craig Blackstone, et al.Annals of Clinical and Translational Neurology|March 22, 2018
Nucleocytoplasmic transport defect in a North American patient with ALS8Robert D Guber, Alice B Schindler, Maher S Budron, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 29, 2026
The spinal and bulbar muscular atrophy-health index: a disease-specific outcome measureAbdullah Alqahtani, Jennifer Weinstein, Angela Kokkinis, et al.Muscle & Nerve|September 7, 2017
Patient-identified impact of symptoms in spinal and bulbar muscular atrophyRobert D Guber, Angela D Kokkinis, Alice B Schindler, et al.Pageof 3