Autoantibodies to thyroid hormones: the role of thyroglobulin von ERRE GRAGUI, K., CHEILLAN, F., DEFOORT, J. P., PRATO, S., FERT, V.

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Comparative study of methods for measuring cholesterol in biological fluids von Cheillan, Franck, Lafont, Huguette, Termine, Elise, Hamann, Yolande, Lesgards, Guy

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Sphingolipid-mediated inflammatory signaling leading to autophagy inhibition converts erythropoiesis to myelopoiesis in human hematopoietic stem/progenitor cells von Orsini, Marion, Chateauvieux, Sébastien, Rhim, Jiyun, Gaigneaux, Anthoula, Cheillan, David, Christov, Christo, Dicato, Mario, Morceau, Franck, Diederich, Marc

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Creatine biosynthesis and transport in health and disease von Joncquel-Chevalier Curt, Marie, Voicu, Pia-Manuela, Fontaine, Monique, Dessein, Anne-Frédérique, Porchet, Nicole, Mention-Mulliez, Karine, Dobbelaere, Dries, Soto-Ares, Gustavo, Cheillan, David, Vamecq, Joseph

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Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model von Martins, Carla, Hůlková, Helena, Dridi, Larbi, Dormoy-Raclet, Virginie, Grigoryeva, Lubov, Choi, Yoo, Langford-Smith, Alexander, Wilkinson, Fiona L, Ohmi, Kazuhiro, DiCristo, Graziella, Hamel, Edith, Ausseil, Jerôme, Cheillan, David, Moreau, Alain, Svobodová, Eva, Hájková, Zuzana, Tesařová, Markéta, Hansíková, Hana, Bigger, Brian W, Hrebícek, Martin, Pshezhetsky, Alexey V

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Tuberous xanthomatosis is not necessarily associated with increased plasma concentrations of cholestanol in cerebrotendinous xanthomatosis von Bonnet, Jean‐Baptiste, Couvert, Philippe, Di‐filippo, Mathilde, Boissiere, Florian, Cristol, Jean‐Paul, Sutra, Thibault, Cheillan, David, Moulin, Philippe, Sultan, Ariane

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Application of a Novel Algorithm for Expanding Newborn Screening for Inherited Metabolic Disorders across Europe von Jones, Simon A, Cheillan, David, Chakrapani, Anupam, Church, Heather J, Heales, Simon, Wu, Teresa H Y, Morton, Georgina, Roberts, Patricia, Sluys, Erica F, Burlina, Alberto

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A New Approach to Objectively Evaluate Inherited Metabolic Diseases for Inclusion on Newborn Screening Programmes von Burlina, Alberto, Jones, Simon A, Chakrapani, Anupam, Church, Heather J, Heales, Simon, Wu, Teresa H Y, Morton, Georgina, Roberts, Patricia, Sluys, Erica F, Cheillan, David

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Newborn screening for cystic fibrosis in France von Munck, Anne, Cheillan, David, Audrezet, Marie-Pierre, Guenet, David, Huet, Frédéric

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Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010 von Loeber, J Gerard, Platis, Dimitris, Zetterström, Rolf H, Almashanu, Shlomo, Boemer, François, Bonham, James R, Borde, Patricia, Brincat, Ian, Cheillan, David, Dekkers, Eugenie, Dimitrov, Dobry, Fingerhut, Ralph, Franzson, Leifur, Groselj, Urh, Hougaard, David, Knapkova, Maria, Kocova, Mirjana, Kotori, Vjosa, Kozich, Viktor, Kremezna, Anastasiia, Kurkijärvi, Riikka, La Marca, Giancarlo, Mikelsaar, Ruth, Milenkovic, Tatjana, Mitkin, Vyacheslav, Moldovanu, Florentina, Ceglarek, Uta, O'Grady, Loretta, Oltarzewski, Mariusz, Pettersen, Rolf D, Ramadza, Danijela, Salimbayeva, Damilya, Samardzic, Mira, Shamsiddinova, Markhabo, Songailiené, Jurgita, Szatmari, Ildiko, Tabatadze, Nazi, Tezel, Basak, Toromanovic, Alma, Tovmasyan, Irina, Usurelu, Natalia, Vevere, Parsla, Vilarinho, Laura, Vogazianos, Marios, Yahyaoui, Raquel, Zeyda, Maximilian, Schielen, Peter C J I

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Polar lipid composition of bioactive dairy co-products buttermilk and butterserum: Emphasis on sphingolipid and ceramide isoforms von Bourlieu, Claire, Cheillan, David, Blot, Marielle, Daira, Patricia, Trauchessec, Michèle, Ruet, Séverine, Gassi, Jean-Yves, Beaucher, Eric, Robert, Benoit, Leconte, Nadine, Bouhallab, Saïd, Gaucheron, Frédéric, Gésan-Guiziou, Geneviève, Michalski, Marie-Caroline

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Potential Role of Sphingolipidoses-Associated Lysosphingolipids in Cancer von Dubot, Patricia, Astudillo, Leonardo, Therville, Nicole, Carrié, Lorry, Pettazzoni, Magali, Cheillan, David, Stirnemann, Jérôme, Levade, Thierry, Andrieu-Abadie, Nathalie, Sabourdy, Frédérique

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Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France von Levaillant, L., Huet, F., Bretones, P., Corne, C., Dupuis, C., Reynaud, R., Somma, C., Barat, P., Corcuff, J.B., Bouhours-Nouet, N., Gauthereau, V., Polak, M., Leger, J., Cheillan, D., Coutant, R.

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Management of X-linked adrenoleukodystrophy in Morocco: actual situation von Benjelloun, F Z Madani, Kriouile, Y, Cheillan, D, Daoud-Tetouani, H, Chabraoui, L

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Steroid Profiling by Tandem Mass Spectrometry Improves the Positive Predictive Value of Newborn Screening for Congenital Adrenal Hyperplasia von Minutti, Carla Z., Lacey, Jean M., Magera, Mark J., Hahn, Si Houn, McCann, Mark, Schulze, Andreas, Cheillan, David, Dorche, Claude, Chace, Donald H., Lymp, James F., Zimmerman, Donald, Rinaldo, Piero, Matern, Dietrich

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Reply to Maase et al. Comment on "Jones et al. Application of a Novel Algorithm for Expanding Newborn Screening for Inherited Metabolic Disorders across Europe. Int. J. Neonatal Sc... von Jones, Simon A, Cheillan, David, Chakrapani, Anupam, Church, Heather J, Heales, Simon, Wu, Teresa H Y, Morton, Georgina, Roberts, Patricia, Sluys, Erica F, Burlina, Alberto

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Creatine deficiency syndrome. A treatable myopathy due to arginine–glycine amidinotransferase (AGAT) deficiency von Nouioua, S, Cheillan, D, Zaouidi, S, Salomons, G.S, Amedjout, N, Kessaci, F, Boulahdour, N, Hamadouche, T, Tazir, M

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Very elevated hCGβ (≥10 multiple of the median) in maternal marker screening for Down syndrome: Frequency, etiologies, outcomes, and guidelines von Dreux, Sophie, Rosenblatt, Jonathan, Benachi, Alexandra, Voirin‐Mathieu, Etienne, Muller, Françoise, Boitte, F., Denis, M. C., Lorenter, P., Jouval, M., Sitruk, B., Suybeng, V., Herbreteau, S., Treyssac, F., Gras, V., Guiot, J., Savarit, D., Blouin, P., Zanusso, M., Clément, P., Brossaud, J., Fischer, I., Moineau, M. P., Kerspern, H., Andlauer, P., Gaeremynck, E., Berchiche, S., Barba, F., Lebrun, C., Terrier, N., Kemeny, S., Delevallée, C., Marceau, G., Gehrke, C., Lemaire, S., Ménégaut, L., Lefaure, G., Petit, V., Gauchez‐Quenin, A. S., Pavili, L., Chevallier‐Helas, F., Artur, F., Sigogneau, P., Groussin, H., Renom, G., Lepers, S., Chianéa, T., Veyrat, B., Le Querler, L., Martin‐Denavit, T., Sault, C., Galland, A., Cheillan, D., Brechard, M. P., Yerokine, P., Levy‐Mozziconacci, A., Toga, C., Sainte‐Rose, M., Wasels, R., Aubertin, D., Rahil, H., Roucaute, T., Boulle, N., Solassol, J., Minery, M., Baillet, C., Dauch, P., Chevillon, I., Masson, D., Rotella, C. M., Barguil, Y., Duhin, M., Got, L., Lachgar, M., Druart, L., Ramirez, J. M., Lacroix, I., Brethome, B., Cassuto, G., Cohen‐Bacrie, M., Ternaux, F., Beaujard, M. P., Annette‐Reisch, M., Bounaud, M. P., Nowak, E., Dossot, J. M., Odaert, H., Quillard Murain, M., Descombes, G., Belot, G., Tisseur, B., Gouneaud, J., Louzier, C., Tosetti, F., Romain, S., Handwerk, L., Molignier, R., De Mas, P., Le Van, M., Estepa, B., Tang, K.

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Do we need congenital adrenal hyperplasia screening for premature infants? von Huet, F, Godefroy, A, Cheillan, D, Somma, C, Roussey, M

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Phenotype and genotype in 101 males with X-linked creatine transporter deficiency von van de Kamp, J M, Betsalel, O T, Mercimek-Mahmutoglu, S, Abulhoul, L, Grünewald, S, Anselm, I, Azzouz, H, Bratkovic, D, de Brouwer, A, Hamel, B, Kleefstra, T, Yntema, H, Campistol, J, Vilaseca, M A, Cheillan, D, D’Hooghe, M, Diogo, L, Garcia, P, Valongo, C, Fonseca, M, Frints, S, Wilcken, B, von der Haar, S, Meijers-Heijboer, H E, Hofstede, F, Johnson, D, Kant, S G, Lion-Francois, L, Pitelet, G, Longo, N, Maat-Kievit, J A, Monteiro, J P, Munnich, A, Muntau, A C, Nassogne, M C, Osaka, H, Ounap, K, Pinard, J M, Quijano-Roy, S, Poggenburg, I, Poplawski, N, Abdul-Rahman, O, Ribes, A, Arias, A, Yaplito-Lee, J, Schulze, A, Schwartz, C E, Schwenger, S, Soares, G, Sznajer, Y, Valayannopoulos, V, Van Esch, H, Waltz, S, Wamelink, M M C, Pouwels, P J W, Errami, A, van der Knaap, M S, Jakobs, C, Mancini, G M, Salomons, G S

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