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Alloisoleucine in isovaleric acidaemia.
Rabier D, Parvy P, Bardet J, Saudubray JM, Kamoun P. Rabier D, et al. Among authors: bardet j. J Inherit Metab Dis. 1992;15(1):154-5. doi: 10.1007/BF01800358. J Inherit Metab Dis. 1992. PMID: 1583870 No abstract available.
A false hyperglycinaemia.
Parvy P, Bardet J, Rabier D, Nedellec J, Kamoun P. Parvy P, et al. Among authors: bardet j. J Inherit Metab Dis. 1991;14(1):112. doi: 10.1007/BF01804401. J Inherit Metab Dis. 1991. PMID: 1861452 No abstract available.
Dicarboxylic aminoaciduria.
Kamoun P, Parvy P, Rabier D, Bardet J, Billette de Villemeur T, Saudubray JM. Kamoun P, et al. Among authors: bardet j. J Inherit Metab Dis. 1994;17(6):758. doi: 10.1007/BF00712024. J Inherit Metab Dis. 1994. PMID: 7707705 No abstract available.
Clinical outcome and long-term management of 17 patients with propionic acidaemia.
van der Meer SB, Poggi F, Spada M, Bonnefont JP, Ogier H, Hubert P, Depondt E, Rapoport D, Rabier D, Charpentier C, Parvy P, Bardet J, Kamoun P, Saudubray JM. van der Meer SB, et al. Among authors: bardet j. Eur J Pediatr. 1996 Mar;155(3):205-10. doi: 10.1007/BF01953939. Eur J Pediatr. 1996. PMID: 8929729
Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?
Rabier D, Diry C, Rotig A, Rustin P, Heron B, Bardet J, Parvy P, Ponsot G, Marsac C, Saudubray JM, Munnich A, Kamoun P. Rabier D, et al. Among authors: bardet j. J Inherit Metab Dis. 1998 Jun;21(3):216-9. doi: 10.1023/a:1005391300203. J Inherit Metab Dis. 1998. PMID: 9686360 No abstract available.
176 results