Effect of intermittent glutamine supplementation on skeletal muscle is not long-lasting in very old rats von Meynial-Denis, Dominique, Beaufrere, A. -M, Mignon, M, Patureau Mirand, P

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The challenge of prenatal identification of congenital diaphragmatic hernia in the context of hydrops von Rossi, A, Delabaere, A, Delmas-Laurichesse, H, Beaufrère, A.M, Lémery, D, Gallot, D

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Prenatal diagnosis of thrombosis of the dural sinuses: report of six cases, review of the literature and suggested management von Laurichesse Delmas, H., Winer, N., Gallot, D., Lopes, K., Perrotin, F., Fluncker, S., Geissler, F., Beaufrere, A. M., Vendittelli, F., Couture, C., Lemery, D.

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Long-term intermittent glutamine supplementation repairs intestinal damage (structure and functional mass) with advanced age: Assessment with plasma citrulline in a rodent model von Beaufrere, A. M, Neveux, N, Patureau Mirand, P, Buffiere, C, Marceau, G, Sapin, V, Cynober, L, Meynial-Denis, Dominique

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Contribution of immature muscle precursors to myositis pathogenesis: a source of type I interferon and a possible target of the immune attack von Tournadre, A, Lenief, V, Beaufrére, A M, Eljaafari-Dany, Assia, Miossec, P

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Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p von Goumy, C., Beaufrère, A. M., Tchirkov, A., Gouas, L., Gaspard, F., Giollant, M., Roucaute, T., Veronèse, L., Lemery, D., Vago, P.

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Prenatal detection of mosaic isochromosome 20q: a fourth report with abnormal phenotype von Goumy, C., Beaufrère, A. M., Francannet, C., Tchirkov, A., Laurichesse Delmas, H., Geissler, F., Lemery, D., Dechelotte, P. J., Vago, P.

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Long-term intermittent glutamine supplementation repairs intestinal damage (structure and functional mass) with advanced age: Assessment with plasma citrulline in a rodent model von Beaufrere, A. M., Neveux, N., Patureau Mirand, P., Buffiere, C., Marceau, G., Sapin, V., Cynober, L., Meynial-Denis, Dominique

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First‐trimester features of Fowler syndrome (hydrocephaly–hydranencephaly proliferative vasculopathy) von Laurichesse‐Delmas, H., Beaufrère, A. M., Martin, A., Kaemmerlen, A. G., Déchelotte, P., Lémery, D.

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X-linked myopathy with excessive autophagy: a clinicopathological study of five new families von Chabrol, B., Figarella-Branger, D., Coquet, M., Mancini, J., Fontan, D., Pedespan, J.M., Francannet, C., Pouget, J., Beaufrère, A.M., Pellissier, J.F.

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Recurrent congenital pulmonary lymphangiectasia von Delabaere, A., Laurichesse‐Delmas, H., Varlet, M. N., Clemenson, A., Dechelotte, P. J., Beaufrere, A. M., Jacquetin, B., Lemery, D., Gallot, D.

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Fetal umbilical cord ligation under ultrasound guidance von Lemery, D. J., Vanlieferinghen, P., Gasq, M., Finkeltin, F., Beaufrere, A. M., Beytout, M.

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OP03.16: Prenatal detection of thromboses of the dural sinuses: report of five cases, diagnosis and outcome von Laurichesse Delmas, H., Winer, N., Talmant, C., Gallot, D., Couture, A., Geissler, F., Beaufrere, A. M., Dechelotte, P. J., Lemery, D.

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Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease von Denamur, Erick, Delezoide, Anne-Lise, Alberti, Corinne, Bourillon, Agnès, Gubler, Marie-Claire, Bouvier, Raymonde, Pascaud, Olivier, Elion, Jacques, Grandchamp, Bernard, Michel-Calemard, Laurence, Missy, Pascale, Zaccaria, Isabelle, Le Nagard, Hervé, Gerard, Bénédicte, Loirat, Chantal

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Pancreatic involvement in Wegener's granulomatosis: a rare and difficult diagnosis von Marroun, I, Delèvaux, I, André, M, Gavet, F, Beaufrere, A M, Slim, K, Aumaître, O

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Congenital Adrenal Hypoplasia Due to Isolated Familial ACTH Deficiency von Déchelotte, P., Darcha, C., Labbé, A., Vanlieféringhen, Ph, Beaufrére, A. M., Malpuech, G.

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Sudden unexpected death in an infant due to a ruptured coronary aneurysm revealing Kawasaki disease von Vanlieferinghen, P-H, Brunet, F, Beaufrère, A M, Borderon, C, Déchelotte, P

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Diagnostic anténatal des tumeurs cérébrales fœtales et diagnostics différentiels von Desvignes, F., Beaufrère, A.-M., Biard, M., Déchelotte, P., Laurichesse-Delmas, H., Lemery, D., Gallot, D.

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Trois bonnes raisons de révéler un déficit en CPT2. À propos d’une observation von Présumey, P., Guettrot-Imbert, G., Delèvaux, I., Andre, M., Beaufrère, A.-M., Aumaitre, O.

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Une polymyosite résistante révélant une dysferlinopathie von Bardy, A., Guettrot-Imbert, G., Delèvaux, I., Beaufrère, A.-M., Krahn, M., André, M., Aumaitre, O.

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