Clinical and biochemical phenotype in 11 patients with mevalonic aciduria von HOFFMANN, G. F, CHARPENTIER, C, TREFZ, F. K, RATING, D, BREMER, H. J, NYHAN, W. L, MAYATEPEK, E, MANCINI, J, LEICHSENRING, M, GIBSON, K. M, DIVRY, P, HREBICEK, M, LEHNERT, W, SARTOR, K

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Combined liver-kidney transplantation in primary hyperoxaluria type 1 von Cochat, P, Gaulier, J M, Koch Nogueira, P C, Feber, J, Jamieson, N V, Rolland, M O, Divry, P, Bozon, D, Dubourg, L

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Seventeen novel mutations that cause profound biotinidase deficiency von Wolf, B, Jensen, K, Hüner, G, Demirkol, M, Baykal, T, Divry, P, Rolland, M.-O, Perez-Cerdá, C, Ugarte, M, Straussberg, R, Basel-Vanagaite, L, Baumgartner, E.R, Suormala, T, Scholl, S, Das, A.M, Schweitzer, S, Pronicka, E, Sykut-Cegielska, J

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A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency von Touma, E H, Rashed, M S, Vianey-Saban, C, Sakr, A, Divry, P, Gregersen, N, Andresen, B S

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Mevalonic aciduria and hyper‐IgD syndrome: Two sides of the same coin? von Tsimaratos, M., Kone‐Paut, I., Divry, P., Philip, N., Chabrol, B.

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N-acetylaspartylglutamate in Canavan disease : an adverse effector? von BURLINA, A. P, FERRARI, V, DIVRY, P, GRADOWSKA, W, JAKOBS, C, BENNETT, M. J, SEWELL, A. C, DIONISI-VICI, C, BURLINA, A. B

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Diagnosis of inborn errors of metabolism by acylcarnitine profiling in blood using tandem mass spectrometry von Vianey‐Saban, C., Guffon, N., Delolne, F., Guibaud, P., Mathieu, M., Divry, P.

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An Adult Form of L-2-Hydroxyglutaric Aciduria Revealed by Tremor von Clerc, C., Bataillard, M., Richard, P., Divry, P., Kraehenbuhl, J., Rumbach, L.

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Succinyl‐CoA:acetoacetate transferase deficiency. Identification of a new case; prenatal exclusion in three further pregnancies von Rolland, M. O., Guffon, N., Mandon, G., Divry, P.

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Determination of total fatty acids in plasma: cis‐5‐Tetradecenoic acid (C14:1ω‐9) in the diagnosis of long‐chain fatty acid oxidation defects von Divry, P., Vianey‐Saban, C., Mathieu, M.

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Plasma free fatty acids in mitochondrial fatty acid oxidation defects von Martı́nez, G, Jiménez-Sánchez, G, Divry, P, Vianey-Saban, C, Riudor, E, Rodés, M, Briones, P, Ribes, A

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Antenatal expression of multiple acyl‐CoA dehydrogenase deficiency von Vianey‐Saban, C., Bouvier, R., Cochat, P., Buenerd, A., Divry, P., Dumoulin, R., Cordier, M. P.

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The mutational spectrum in very long‐chain acyl‐CoA dehydrogenase deficiency von Andresen, B. S., Vianey‐Saban, C., Bross, P., Divry, P., Roe, C. R., Nada, M. A., Knudsen, I., Gregersen, N.

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The inborn errors of mitochondrial fatty acid oxidation von Vianey‐Liaud, C., Divry, P., Gregersen, N., Mathieu, M.

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l‐2‐Hydroxyglutaric aciduria: Two further cases von Divry, P., Jakobs, C., Vianey‐Saban, C., Gibson, K. M., Michelakakis, H., Papadimitriou, A., Divari, R., Chabrol, B., Cournelle, M. A., Livet, M. O.

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2‐Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: Report of a new case von Guffon, N., Lopez‐Mediavilla, C., Dumoulin, R., Mousson, B., Godinot, C., Carrier, H., Collombet, J. M., Divry, P., Mathieu, M., Guibaud, P.

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Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients von Vianey-Saban, Christine, Divry, Priscille, Brivet, Michèle, Nada, Mohamed, Zabot, Marie-Thérèse, Mathieu, Monique, Roe, Charles

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Reliable prenatal diagnosis of Canavan disease (aspartoacylase deficiency): Comparison of enzymatic and metabolite analysis von Bennett, M. J., Gibson, K. M., Sherwood, W. G., Divry, P., Rolland, M. O., Elpeleg, O. N., Rinaldo, P., Jakobs, C.

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Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia von VIANEY-SABAN, C, MOUSSON, B, BERTRAND, C, STAMM, D, DUMOULIN, R, ZABOT, M. T, DIVRY, P, FLORET, D, MATHIEU, M

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Lethal dilated cardiomyopathy due to long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency von Martins, E., Costa, A., Silva, E., Medina, M., Cardoso, M. L., Vianey‐Saban, C., Divry, P., Vilarinho, L.

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