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Page 1
Familial encephalopathy and L-2-hydroxyglutaric aciduria.
Kaabachi N, Larnaout A, Rabier D, Jakobs C, Belal S, Hentati F, Parvey P, Bardet J, Ben Hamida M, Mebazaa A, et al. Kaabachi N, et al. Among authors: bardet j. J Inherit Metab Dis. 1993;16(5):893. doi: 10.1007/BF00714285. J Inherit Metab Dis. 1993. PMID: 8295407 No abstract available.
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.
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.
177 results