Nutritional modulation of the intestinal microbiota; future opportunities for the prevention and treatment of neuroimmune and neuroinflammatory disease von Lombardi, Vincent C., De Meirleir, Kenny L., Subramanian, Krishnamurthy, Nourani, Sam M., Dagda, Ruben K., Delaney, Shannon L., Palotás, András

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Mucosal Immunity and the Gut-Microbiota-Brain-Axis in Neuroimmune Disease von Sterling, Kathryn G, Dodd, Griffin Kutler, Alhamdi, Shatha, Asimenios, Peter G, Dagda, Ruben K, De Meirleir, Kenny L, Hudig, Dorothy, Lombardi, Vincent C

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Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12 von De Meirleir, L, Seneca, S, Lissens, W, De Clercq, I, Eyskens, F, Gerlo, E, Smet, J, Van Coster, R

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Myalgic encephalomyelitis: International Consensus Criteria von Carruthers, B. M., van de Sande, M. I., De Meirleir, K. L., Klimas, N. G., Broderick, G., Mitchell, T., Staines, D., Powles, A. C. P., Speight, N., Vallings, R., Bateman, L., Baumgarten‐Austrheim, B., Bell, D. S., Carlo‐Stella, N., Chia, J., Darragh, A., Jo, D., Lewis, D., Light, A. R., Marshall‐Gradisbik, S., Mena, I., Mikovits, J. A., Miwa, K., Murovska, M., Pall, M. L., Stevens, S.

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A multicenter study on Leigh syndrome: disease course and predictors of survival von Sofou, Kalliopi, De Coo, Irenaeus F M, Isohanni, Pirjo, Ostergaard, Elsebet, Naess, Karin, De Meirleir, Linda, Tzoulis, Charalampos, Uusimaa, Johanna, De Angst, Isabell B, Lönnqvist, Tuula, Pihko, Helena, Mankinen, Katariina, Bindoff, Laurence A, Tulinius, Már, Darin, Niklas

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Evaluation of four clinical laboratory parameters for the diagnosis of myalgic encephalomyelitis von De Meirleir, Kenny L, Mijatovic, Tatjana, Subramanian, Krishnamurthy, Schlauch, Karen A, Lombardi, Vincent C

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Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy von Wraith, J. Edmond, Scarpa, Maurizio, Beck, Michael, Bodamer, Olaf A., De Meirleir, Linda, Guffon, Nathalie, Meldgaard Lund, Allan, Malm, Gunilla, Van der Ploeg, Ans T., Zeman, Jiri

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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C von Dermaut, B, Seneca, S, Dom, L, Smets, K, Ceulemans, L, Smet, J, De Paepe, B, Tousseyn, S, Weckhuysen, S, Gewillig, M, Pals, P, Parizel, P, De Bleecker, J L, Boon, P, De Meirleir, L, De Jonghe, P, Van Coster, R, Van Paesschen, W, Santens, P

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Mutational study in the PDHA1 gene of 40 patients suspected of pyruvate dehydrogenase complex deficiency von Quintana, E, Gort, L, Busquets, C, Navarro-Sastre, A, Lissens, W, Moliner, S, Lluch, M, Vilaseca, MA, De Meirleir, L, Ribes, A, Briones, P

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ALG11-CDG: Three novel mutations and further characterization of the phenotype von Regal, L., van Hasselt, P.M., Foulquier, F., Cuppen, I., Prinsen, HCMT, Jansen, K., Keldermans, L., De Meirleir, L., Matthijs, G., Jaeken, J.

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Biomedical approach in autism spectrum disorders—the importance of assessing inflammation von Mijatovic, Tatjana, Siniscalco, Dario, Subramanian, Krishnamurthy, Bosmans, Eugene, C. Lombardi, Vincent, L. De Meirleir, Kenny

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Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth re... von Molema, Femke, Gleich, Florian, Burgard, Peter, van der Ploeg, Ans T., Summar, Marshall L., Chapman, Kimberly A., Lund, Allan M., Rizopoulos, Dimitris, Kölker, Stefan, Williams, Monique, Hörster, F., Jelsig, A.M., de Lonlay, P., Wijburg, F.A., Bosch, A., Freisinger, P., Posset, R., Augoustides-Savvopoulou, P., Avram, P., Deleanu, C., Baumgartner, M.R., Häberle, J., Blasco-Alonso, J., Burlina, A.B., Rubert, L., Cazorla, A. Garcia, Saladelafont, E. Cortes I., Dionisi-Vici, C., Martinelli, D., Dobbelaere, D., Mention, K., Grünewald, S., Chakrapani, A., Hwu, Wuh-Liang, Chien, Yin-Hsiu, Lee, Ni-Chung, Karall, D., Scholl-Bürgi, S., De Laet, C., Matsumoto, S., de Meirleir, L., Schiff, M., Peña-Quintana, L., Djordjevic, M., Sarajlija, A., Sykut-Cegielska, J., Wisniewska, A., Leao-Teles, E., Alves, S., Vara, R., Vives-Pinera, I., Gil-Ortega, D., Morris, A., Zeman, J., Honzik, T., Chabrol, B., Arnaudo, F., Cano, A., Thompson, N., Eyskens, F., Lindner, M., Lüsebrink, N., Jalan, A., Sokal, E., Legros, V., Nassogne, M.C., Barić, I.

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Mutations in SACS cause atypical and late-onset forms of ARSACS von BAETS, J, DECONINCK, T, ROBBERECHT, W, DE MEIRLEIR, L, MICHIELSENS, B, DEL-FAVERO, J, JORDANOVA, A, DE JONGHE, P, SMETS, K, GOOSSENS, D, VAN DEN BERGH, P, DAHAN, K, SCHMEDDING, E, SANTENS, P, MILIC RASIC, V, VAN DAMME, P

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TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria von Jansen, A C, Oostra, A, Desprechins, B, De Vlaeminck, Y, Verhelst, H, Régal, L, Verloo, P, Bockaert, N, Keymolen, K, Seneca, S, De Meirleir, L, Lissens, W

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Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data von Huemer, M., Bürer, C., Ješina, P., Kožich, V., Landolt, M. A., Suormala, T., Fowler, B., Augoustides- Savvopoulou, P., Blair, E., Brennerova, K., Broomfield, A., De Meirleir, L., Gökcay, G., Hennermann, J., Jardine, P., Koch, J., Lorenzl, S., Lotz-Havla, A. S., Noss, J., Parini, R., Peters, H., Plecko, B., Ramos, F. J., Schlune, A., Tsiakas, K., Zerjav Tansek, M., Baumgartner, M. R.

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Aminoacylase I deficiency: A novel inborn error of metabolism von Van Coster, R.N., Gerlo, E.A., Giardina, T.G., Engelke, U.F., Smet, J.E., De Praeter, C.M., Meersschaut, V.A., De Meirleir, L.J., Seneca, S.H., Devreese, B., Leroy, J.G., Herga, S., Perrier, J.P., Wevers, R.A., Lissens, W.

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Increased D-Lactic Acid Intestinal Bacteria in Patients with Chronic Fatigue Syndrome von Sheedy, John R, Wettenhall, Richard E H, Scanlon, Denis, Gooley, Paul R, Lewis, Donald P, McGregor, Neil, Stapleton, David I, Butt, Henry L, DE Meirleir, Kenny L

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Complex phenotype associated with mutation in the TANGO2 gene von De Meirleir, L, D'Hooghe, M, De Rademaeker, M, Stouffs, K, Geldhof, A, Seneca, S

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Single-nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases von Schlauch, Karen A., Kulick, Doina, Subramanian, Krishnamurthy, De Meirleir, Kenny L., Palotás, András, Lombardi, Vincent C.

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Progress in Paediatric Neurology Research Conference, Leuven, Belgium, October 1–2, 2010 von De Meirleir, L

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