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Neurology|August 10, 2000
Retrospective analysis of the use of cyclosporine in myasthenia gravisE Ciafaloni, N K Nikhar, J M Massey, et al.Neurology|January 10, 2001
Mycophenolate mofetil for myasthenia gravis: an open-label pilot studyE Ciafaloni, J M Massey, B Tucker-Lipscomb, et al.Journal of the Neurological Sciences|September 1, 1992
Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNAA Suomalainen, E Ciafaloni, Y Koga, et al.Annals of Neurology|June 1, 1991
Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromesM L Zupanc, C T Moraes, S Shanske, et al.The Journal of Pediatrics|March 1, 1993
Maternally inherited Leigh syndromeE Ciafaloni, F M Santorelli, S Shanske, et al.Archives of Neurology|March 1, 1993
The syndrome of mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes presenting without strokeR K Mosewich, J R Donat, S DiMauro, et al.Neurology|November 30, 2006
Pregnancy and birth outcomes in women with facioscapulohumeral muscular dystrophyE Ciafaloni, E K Pressman, A M Loi, et al.Neurology|June 1, 1993
Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation")G Silvestri, E Ciafaloni, F M Santorelli, et al.Clinical Neuropathology|July 1, 1991
Muscle biopsy in Alzheimer's disease: morphological and biochemical findingsC Mariani, N Bresolin, E Farina, et al.Pageof 2