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American Journal of Human Genetics|February 1, 1991
Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF)M Zeviani, P Amati, N Bresolin, et al.European Journal of Clinical Pharmacology|January 1, 1985
Effects of pirenzepine on plasma insulin, glucagon and pancreatic polypeptide levels in normal manM Zaccaria, G Giordano, C Pasquali, et al.Annals of Neurology|July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathiesM Zeviani, C Gellera, M Pannacci, et al.Human Molecular Genetics|February 1, 1997
A single cell complementation class is common to several cases of cytochrome c oxidase-defective Leigh's syndromeM Munaro, V Tiranti, D Sandonà, et al.Neurology|March 1, 1990
Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymesC Gellera, G Uziel, M Rimoldi, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 25, 2005
Devic's neuromyelitis optica and mitochondrial DNA mutation: a case reportA Ghezzi, S Baldini, M Zaffaroni, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six familiesG Uziel, I Moroni, E Lamantea, et al.Human Molecular Genetics|April 1, 1997
Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags databaseV Tiranti, A Savoia, F Forti, et al.Neuromuscular Disorders : NMD|April 30, 1999
A novel mutation (8342G-->A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonusV Tiranti, F Carrara, P Confalonieri, et al.Electrophoresis|September 23, 2000
Separation of intact pyruvate dehydrogenase complex using blue native agarose gel electrophoresisN S Henderson, L G Nijtmans, J G Lindsay, et al.Pageof 18