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Journal of the Neurological Sciences|January 6, 2000
Longitudinal analysis of the segregation of mtDNA mutations in heteroplasmic individualsN Howell, S S Ghosh, E Fahy, et al.Journal of Internal Medicine|February 5, 2009
Batteries not included: diagnosis and management of mitochondrial diseaseR McFarland, D M TurnbullJournal of Neurology, Neurosurgery, and Psychiatry|November 1, 1985
The comparative efficacy of antiepileptic drugs for partial and tonic-clonic seizuresD Chadwick, D M TurnbullActa Neurologica Scandinavica|September 12, 2009
A novel mutation in the mitochondrial tRNA for tryptophan causing a late-onset mitochondrial encephalomyopathyP S Sanaker, H L Nakkestad, E Downham, et al.Clinical Neurology and Neurosurgery|August 1, 1997
Spontaneous intracranial hypotension: clinical and magnetic resonance imaging characteristicsS C Blank, R A Shakir, L A Bindoff, et al.Acta Neurologica Scandinavica. Supplementum|April 11, 2007
Clinical evolution of Kearns-Sayre syndrome with polyendocrinopathy and respiratory failureP S Sanaker, E S Husebye, O Fondenes, et al.Quarterly Journal of Experimental Physiology (Cambridge, England)|April 1, 1984
Mitochondrial oxidative enzyme activity in individual fibre types in hypo- and hyperthyroid rat skeletal musclesM A Johnson, D M TurnbullCurrent Opinion in Neurology|December 1, 1994
Metabolic disorders in childrenA A Morris, D M TurnbullJournal of Inherited Metabolic Disease|January 1, 1996
Disorders of the electron transport chainP L Adams, D M TurnbullPageof 22