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European Neurology|January 1, 1990
Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapyA Federico, M T Dotti, G M Fabrizi, et al.
The Journal of Physical Chemistry. A|January 30, 2007
Comparison of static first hyperpolarizabilities calculated with various quantum mechanical methodsC M Isborn, A Leclercq, F D Vila, et al.
The New England Journal of Medicine|July 30, 1992
A bovine albumin peptide as a possible trigger of insulin-dependent diabetes mellitusJ Karjalainen, J M Martin, M Knip, et al.
American Journal of Human Genetics|March 1, 1984
The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiencyB H Robinson, J Oei, W G Sherwood, et al.
The Journal of Biological Chemistry|August 10, 1984
Interactions and spatial arrangement of spin-labeled NAD+ bound to glyceraldehyde-3-phosphate dehydrogenase. Comparison of EPR and X-ray modeling dataA H Beth, B H Robinson, C E Cobb, et al.
American Journal of Human Genetics|April 1, 1992
Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is highY Tatuch, J Christodoulou, A Feigenbaum, et al.
British Medical Journal|March 6, 1976
Results of 250 consecutive cadaver kidney transplantsC L Hall, J R Sansom, M Obeid, et al.
Human Molecular Genetics|April 18, 1998
Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.
The American Journal of Physiology|November 14, 1998
Myocardial aerobic metabolism is impaired in a cell culture model of cyanotic heart diseaseF Merante, D A Mickle, R D Weisel, et al.
Human Genetics|February 3, 2009
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotypeJ M Cameron, M Maj, V Levandovskiy, et al.
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