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595 results

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Page 1
Metabolic intermediates in lactic acidosis: compounds, samples and interpretation.
Poggi-Travert F, Martin D, Billette de Villemeur T, Bonnefont JP, Vassault A, Rabier D, Charpentier C, Kamoun P, Munnich A, Saudubray JM. Poggi-Travert F, et al. Among authors: charpentier c. J Inherit Metab Dis. 1996;19(4):478-88. doi: 10.1007/BF01799109. J Inherit Metab Dis. 1996. PMID: 8884572 Review.
Attempt at therapy in sulphite oxidase deficiency.
Tardy P, Parvy P, Charpentier C, Bonnefont JP, Saudubray JM, Kamoun P. Tardy P, et al. Among authors: charpentier c. J Inherit Metab Dis. 1989;12(1):94-5. doi: 10.1007/BF01805537. J Inherit Metab Dis. 1989. PMID: 2501590 No abstract available.
[Diagnosis of metabolic coma in children].
Poggi-Travert F, Héron B, Billette de Villemeur T, Spada M, Jouvet P, Charpentier C, Rabier D, Kamoun P, Saudubray JM. Poggi-Travert F, et al. Among authors: charpentier c. Arch Pediatr. 1994 Sep;1(9):843-51. Arch Pediatr. 1994. PMID: 7842129 Review. French.
Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6-C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?
Poll-The BT, Bonnefont JP, Ogier H, Charpentier C, Pelet A, Le Fur JM, Jakobs C, Kok RM, Duran M, Divry P, et al. Poll-The BT, et al. Among authors: charpentier c. J Inherit Metab Dis. 1988;11 Suppl 2:183-5. doi: 10.1007/BF01804230. J Inherit Metab Dis. 1988. PMID: 2846959 No abstract available.
Hyperketotic states due to inherited defects of ketolysis.
Saudubray JM, Specola N, Middleton B, Lombes A, Bonnefont JP, Jakobs C, Vassault A, Charpentier C, Day R. Saudubray JM, et al. Among authors: charpentier c. Enzyme. 1987;38(1-4):80-90. doi: 10.1159/000469194. Enzyme. 1987. PMID: 2894307 Review.
595 results