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Acta Neuropathologica|January 1, 1992
Alexander's disease in infancy and childhood: a report of two casesJ W Neal, E M Cave, S K Singhrao, et al.Journal of Animal Science|July 24, 2001
Influence of supplementary fibrolytic enzymes on the fermentation of corn and grass silages by mixed ruminal microorganisms in vitroR J Wallace, S J Wallace, N McKain, et al.Pediatric Research|December 1, 1994
Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1 alpha mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathyL De Meirleir, W Lissens, C Benelli, et al.Human Mutation|April 24, 2001
Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome C oxidase deficiencyM O Péquignot, R Dey, M Zeviani, et al.Neuromuscular Disorders : NMD|September 1, 1993
Merrf family with 8344 mutation in tRNA (lys). Evidence of a mitochondrial vasculopathy in muscle biopsiesM Coquet, F Degoul, A Vital, et al.Transplantation|November 1, 1990
Evidence of mitochondrial impairment during cardiac allograft rejectionD Duboc, P Abastado, M Muffat-Joly, et al.Journal of the Neurological Sciences|August 1, 1983
Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiencyP E Minchom, R L Dormer, I A Hughes, et al.Archives of Disease in Childhood|March 1, 1986
Cotside EEG monitoring using computerised spectral analysisS S Aziz, S J Wallace, J F Murphy, et al.Molecular Phylogenetics and Evolution|November 7, 2016
A phylogenetic test of sympatric speciation in the Hydrobatinae (Aves: Procellariiformes)S J Wallace, J A Morris-Pocock, J González-Solís, et al.The Journal of Pediatrics|December 1, 1995
Lamotrigine for the treatment of epilepsy in childhoodF M Besag, S J Wallace, O Dulac, et al.Pageof 15