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Archives of Disease in Childhood|August 1, 1996
Evaluation of fasts for investigating hypoglycaemia or suspected metabolic diseaseA A Morris, A Thekekara, Z Wilks, et al.Journal of Cardiovascular Pharmacology|September 1, 1979
Cardiotonic effects of anthopleurin-A, a polypeptide from a sea anemoneA Scriabine, C G Van Arman, G Morgan, et al.The Journal of Pediatrics|April 17, 1998
A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotypeA A Morris, S E Olpin, M Brivet, et al.Pediatric Research|September 4, 1998
Hepatic mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme a synthase deficiencyA A Morris, C V Lascelles, S E Olpin, et al.Brain : a Journal of Neurology|April 1, 1995
Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patientsM J Jackson, J A Schaefer, M A Johnson, et al.International Journal of Legal Medicine|August 25, 1999
Expanding the forensic German mitochondrial DNA control region database: genetic diversity as a function of sample size and microgeographyH Pfeiffer, B Brinkmann, J Hühne, et al.Archives of Disease in Childhood|January 31, 2006
Glucose and leucine kinetics in idiopathic ketotic hypoglycaemiaO A Bodamer, K Hussein, A A Morris, et al.Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.Human Molecular Genetics|June 1, 1997
Molecular mechanisms in mitochondrial DNA depletion syndromeJ W Taanman, A G Bodnar, J M Cooper, et al.Archives of Disease in Childhood|October 23, 2001
ARC syndrome: an expanding range of phenotypesK M Eastham, P J McKiernan, D V Milford, et al.Pageof 3