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Chest|September 1, 1992
Transbronchial lung biopsy. Histopathologic and morphometric assessment of diagnostic utilityA E Fraire, S P Cooper, S D Greenberg, et al.Annals of Neurology|February 1, 1979
Emery-Dreifuss muscular dystrophyL P Rowland, M Fetell, M Olarte, et al.Neurology|November 1, 1996
Leigh-type neuropathology in Pearson syndrome associated with impaired ATP production and a novel mtDNA deletionF M Santorelli, M A Barmada, R Pons, et al.Biochemical and Biophysical Research Communications|August 15, 1995
A novel mtDNA point mutation in maternally inherited cardiomyopathyC Casali, F M Santorelli, G D'Amati, et al.Annals of Neurology|June 1, 1983
Kearns-Sayre syndrome with reduced plasma and cerebrospinal fluid folateR J Allen, S DiMauro, D L Coulter, et al.Neurology|March 1, 1980
Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failureT Bertorini, Y Y Yeh, C Trevisan, 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.Neurology|June 1, 1986
Juvenile-onset acid maltase deficiency with unusual familial featuresM J Danon, S DiMauro, S Shanske, et al.Neurology|June 1, 1987
Cardiomyopathy, mental retardation, and autophagic vacuolar myopathyZ H Hart, S Servidei, P L Peterson, et al.Neurology|April 24, 2002
Exercise-induced muscle "burning," fatigue, and hyper-CKemia: mtDNA T10010C mutation in tRNA(Gly)Y Nishigaki, E Bonilla, S Shanske, et al.Pageof 44