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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Defect in the X-lipoyl-containing component of the pyruvate dehydrogenase complex in a patient with a neonatal lactic acidemia von GEOFFROY, V, FOUQUE, F, BENELLI, C, POGGI, F, SAUDUBRAY, J. M, LISSENS, W, MEIRLEIR, L. D, MARSAC, C, LINDSAY, J. G, SANDERSON, S. J

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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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Multiple Phenotypes in Phosphoglucomutase 1 Deficiency von Tegtmeyer, Laura C, Rust, Stephan, van Scherpenzeel, Monique, Ng, Bobby G, Losfeld, Marie-Estelle, Timal, Sharita, Raymond, Kimiyo, He, Ping, Ichikawa, Mie, Veltman, Joris, Huijben, Karin, Shin, Yoon S, Sharma, Vandana, Adamowicz, Maciej, Lammens, Martin, Reunert, Janine, Witten, Anika, Schrapers, Esther, Matthijs, Gert, Jaeken, Jaak, Rymen, Daisy, Stojkovic, Tanya, Laforêt, Pascal, Petit, François, Aumaître, Olivier, Czarnowska, Elzbieta, Piraud, Monique, Podskarbi, Teodor, Stanley, Charles A, Matalon, Reuben, Burda, Patricie, Seyyedi, Soraya, Debus, Volker, Socha, Piotr, Sykut-Cegielska, Jolanta, van Spronsen, Francjan, de Meirleir, Linda, Vajro, Pietro, DeClue, Terry, Ficicioglu, Can, Wada, Yoshinao, Wevers, Ron A, Vanderschaeghe, Dieter, Callewaert, Nico, Fingerhut, Ralph, van Schaftingen, Emile, Freeze, Hudson H, Morava, Eva, Lefeber, Dirk J, Marquardt, Thorsten

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I TUBAIA mutations: I From isolated lissencephaly to familial polymicrogyria von JANSEN, A. C, OOSTRA, A, DE MEIRLEIR, L, LISSENS, W, DESPRECHINS, B, DE VLAEMINCK, Y, VERHELST, H, REGAL, L, VERLOO, P, BOCKAERT, N, KEYMOLEN, K, SENECA, S

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Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene von De Meirleir, Linda, Seneca, Sara, Lissens, Willy, Schoentjes, Eric, Desprechins, Brigette

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Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. Commentary von COMAN, David J, MORAVA, E, RANELLS, J, LEMYRE, E, VAN REEUWIJK, J, BRUNNER, H. G, WEVERS, R. A, LEFEBER, D. J, URBAN, Z, DE MEIRLEIR, L, MEINECKE, P, KAESBACH, G. Gillessen, SYKUT-CEGIELSKA, J, ADAMOWICZ, M, SALAFSKY, I

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Acrodermatitis enteropathica–like cutaneous lesions in organic aciduria von De Raeve, Linda, De Meirleir, Linda, Ramet, José, Vandenplas, Yvan, Gerlo, Erik

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Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1α deficiency von MARSAC, C, BENELLI, C, ZABOT, M.-T, FONTAN, D, LISSENS, W, DESGUERRE, I, DIRY, M, FOUQUE, F, DE MEIRLEIR, L, PONSOT, G, SENECA, S, POGGI, F, SAUDUBRAY, J.-M

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Dancing Eye Syndrome and Hyperphosphatasemia von Hasaerts, Daniele E., Gorus, Frans K., De Meirleir, Linda J.

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Pyruvate dehydrogenase deficiency: Clinical and biochemical diagnosis von De Meirleir, Linda, Lissens, Willy, Denis, Robert, Wayenberg, Jean-Louis, Michotte, Alex, Brucher, Jean-Marie, Vamos, Esther, Gerlo, Erik, Liebaers, Inge

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Pseudallescheria boydii and brain abscesses von HACHIMI-IDRISSI, S, WILLEMSEN, M, DESPRECHINS, B, NAESSENS, A, GOOSSENS, A, MEIRLEIR, L DE, RAMET, J

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Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1α mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathy von DE MEIRLEIR, L, LISSENS, W, BENELLI, C, PONSOT, G, DESGUERRE, I, MARSAC, C, RODRIGUEZ, D, SAUDUBRAY, J.-M, POGGI, F, LIEBAERS, I

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Neuropathological findings of a patient with pyruvate dehydrogenase E1α deficiency presenting as a cerebral lactic acidosis von MICHOTTE, A, DE MEIRLEIR, L, LISSENS, W, DENIS, R, WAYENBERG, J. L, LIEBAERS, I, BRUCHER, J. M

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Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1α subunit von DE MEIRLEIR, L, LISSENS, W, VAMOS, E, LIEBAERS, I

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Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: Clues to pathogenesis of Leigh disease von Robinson, Brian H., De Meirieir, Linda, Glerum, Moira, Sherwood, Geoffrey, Becker, Larry

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Pyruvate dehydrogenase deficiency due to a mutation of the E1 α subunit von Meirleir, L. J., Lissens, W., Vamos, E., Liebaers, I.

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Leigh syndrome due to pyruvate dehydrogenase E1α deficiency (point mutation R263G) in a Spanish boy von Briones, P., López, M. J., De Meirleir, L., Ribes, A., Rodés, M., Martinez‐Costa, C., Peris, M., Lissens, W.

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Importance of sequence analysis in NARP syndrome von Seneca, S., De Meirleir, L., Liebaers, I., Lissens, W.

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Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts von TELLERMAN-TOPPET, N, BIARENT, D, BOUTON, J.-M, DE MEIRLEIR, L, ELMER, C, NOEL, S, VAMOS, E, DIMAURO, S

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