Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome by Snanoudj, Sarah, Mordel, Patrick, Dupas, Quentin, Schanen, Cécile, Arion, Alina, Gérard, Marion, Read, Marie‐Hélène, Nait Rabah, Djamel, Goux, Didier, Chapon, Françoise, Jokic, Mickael, Allouche, Stéphane

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Semi-Elemental Formula or Polymeric Formula: Is There a Better Choice for Enteral Nutrition in Acute Pancreatitis? Randomized Comparative Study by Tiengou, Laurent-Eric, Gloro, Romain, Pouzoulet, Julien, Bouhier, Karine, Read, Marie-Hélène, Arnaud-Battandier, Franck, Plaze, Jean-Marie, Blaizot, Xavier, Dao, Thông, Piquet, Marie-Astrid

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Blood metabolite data in response to maximal exercise in healthy subjects by Mouadil, Amèle, Debout, Claire, Read, Marie-Hélène, Morello, Rémy, Allouche, Stéphane, Chapon, Françoise

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Methods for homocysteine analysis and biological relevance of the results by Ducros, Véronique, Demuth, Karine, Sauvant, Marie-Pierre, Quillard, Muriel, Caussé, Elisabeth, Candito, Mirande, Read, Marie-Hélène, Drai, Jocelyne, Garcia, Isabelle, Gerhardt, Marie-Françoise

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Deficiency in SLC25A1, Encoding the Mitochondrial Citrate Carrier, Causes Combined D-2- and L-2-Hydroxyglutaric Aciduria by Nota, Benjamin, Struys, Eduard A., Pop, Ana, Jansen, Erwin E., Fernandez Ojeda, Matilde R., Kanhai, Warsha A., Kranendijk, Martijn, van Dooren, Silvy J.M., Bevova, Marianna R., Sistermans, Erik A., Nieuwint, Aggie W.M., Barth, Magalie, Ben-Omran, Tawfeg, Hoffmann, Georg F., de Lonlay, Pascale, McDonald, Marie T., Meberg, Alf, Muntau, Ania C., Nuoffer, Jean-Marc, Parini, Rossella, Read, Marie-Hélène, Renneberg, Axel, Santer, René, Strahleck, Thomas, van Schaftingen, Emile, van der Knaap, Marjo S., Jakobs, Cornelis, Salomons, Gajja S.

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Involvement and alteration of the Sonic Hedgehog pathway is associated with decreased cholesterol level in trisomy 18 and SLO amniocytes by Gruchy, N., Bigot, N., Jeanne Pasquier, C., Read, M.H., Odent, S., Galera, P., Leporrier, N.

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Hypotransferrinémie majeure origine congénitale ou acquise ? by Paturel, Elise, Coulbault, Laurent, Read, Marie-Hélène, Krieger, Sophie, Fradin, Sabine, Jauzac, Philippe, Allouche, Stéphane

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A novel mutation in the mitochondrial tRNA{sup Asn} gene associated with a lethal disease by Coulbault, Laurent, Herlicoviez, Danielle, Chapon, Francoise, Read, Marie-Helene, Penniello, Marie-Jose, Reynier, Pascal, Fayet, Guillemette, Lombes, Anne, Jauzac, Philippe, Allouche, Stephane

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A novel mutation in the mitochondrial tRNA Asn gene associated with a lethal disease by Coulbault, Laurent, Herlicoviez, Danielle, Chapon, Françoise, Read, Marie-Hélène, Penniello, Marie-José, Reynier, Pascal, Fayet, Guillemette, Lombès, Anne, Jauzac, Philippe, Allouche, Stéphane

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A novel mutation in the mitochondrial tRNAAsn gene associated with a lethal disease by Coulbault, Laurent, Herlicoviez, Danielle, Chapon, Françoise, Read, Marie-Hélène, Penniello, Marie-José, Reynier, Pascal, Fayet, Guillemette, Lombès, Anne, Jauzac, Philippe, Allouche, Stéphane

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Reviews by Munting, Roger, Soni‐Sinha, Urvashi, Parkes, Stuart, Cornils, Ingo, Wiessala, Georg, Flenley, Paul, Scammell, Margaret, Gorrara, Claire, FOUSKAS, Vassilis, Byrne, Paul, Read, Christopher, Tooze, Hannah, Judson, Tracey, Leaman, Jeremy, Heurtaud‐Wright, Marie‐Hélène, Beaverstock, Jonathan V., Smith, Michael, Lister, Ruth, Threlfall, Monica, Gane, Mike, Grix, Jonathan

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Reviews by Munting, Roger, Soni-Sinha, Urvashi, Parkes, Stuart, Cornils, Ingo, Wiessala, Georg, Flenley, Paul, Scammell, Margaret, Gorrara, Claire, FOUSKAS, Vassilis, Byrne, Paul, Read, Christopher, Tooze, Hannah, Judson, Tracey, Leaman, Jeremy, Heurtaud-Wright, Marie-Hélène, Beaverstock, Jonathan V., Smith, Michael, Lister, Ruth, Threlfall, Monica, Gane, Mike, Grix, Jonathan

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