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Journal of Inherited Metabolic Disease|November 8, 2003
Acute respiratory distress syndrome in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficienciesC T Lundy, J P H Shield, E A Kvittingen, et al.Nature Genetics|January 19, 2002
Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutationRobert McFarland, Kim M Clark, Andrew A M Morris, et al.European Journal of Pediatrics|October 12, 2013
Unsuccessful treatment of severe pyruvate carboxylase deficiency with triheptanoinC Breen, F J White, C A B Scott, et al.Cancer Treatment Reviews|November 15, 2016
Approach to evaluation of fever in ambulatory cancer patients receiving chemotherapy: A systematic reviewM K Krzyzanowska, C Walker-Dilks, A M Morris, et al.Pediatrics|January 5, 2002
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patientsMargarethe E J den Boer, Ronald J A Wanders, Andrew A M Morris, et al.Developmental Medicine and Child Neurology|August 15, 2006
Pyruvate dehydrogenase E3 binding protein (protein X) deficiencyR M Brown, R A Head, A A M Morris, et al.Journal of Inherited Metabolic Disease|January 27, 2005
Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiencyR K J Olsen, M Pourfarzam, A A M Morris, et al.The American Journal of Pathology|July 8, 1999
Mitochondrial DNA depletion syndrome is expressed in amniotic fluid cell culturesJ C Blake, J W Taanman, A M Morris, et al.European Journal of Human Genetics : EJHG|April 1, 2004
A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndromeKatharina Maniura-Weber, Robert W Taylor, Margaret A Johnson, et al.Pageof 12