Combined Enzymatic Complex I and III Deficiency Associated with Mutations in the Nuclear Encoded NDUFS4 Gene von Budde, S.M.S., van den Heuvel, L.P.W.J., Janssen, A.J., Smeets, R.J.P., Buskens, C.A.F., DeMeirleir, L., Van Coster, R., Baethmann, M., Voit, T., Trijbels, J.M.F., Smeitink, J.A.M.

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Gut-Associated Plasmacytoid Dendritic Cells Display an Immature Phenotype and Upregulated Granzyme B in Subjects with HIV/AIDS von Boichuk, Sergei V, Khaiboullina, Svetlana F, Ramazanov, Bulat R, Khasanova, Gulshat R, Ivanovskaya, Karina A, Nizamutdinov, Evgeny Z, Sharafutdinov, Marat R, Martynova, Ekaterina V, DeMeirleir, Kenny L, Hulstaert, Jan, Anokhin, Vladimir A, Rizvanov, Albert A, Lombardi, Vincent C

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Cytokine expression provides clues to the pathophysiology of Gulf War illness and myalgic encephalomyelitis von Khaiboullina, Svetlana F., DeMeirleir, Kenny L., Rawat, Shanti, Berk, Grady S., Gaynor-Berk, Rory S., Mijatovic, Tatjana, Blatt, Natalia, Rizvanov, Albert A., Young, Sheila G., Lombardi, Vincent C.

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Deficiency of mitochondrial ATP synthase of nuclear genetic origin von Sperl, W., Ješina, P., Zeman, J., Mayr, J.A., DeMeirleir, L., VanCoster, R., Pícková, A., Hansíková, H., Houšt’ková, H., Krejčík, Z., Koch, J., Smet, J., Muss, W., Holme, E., Houštěk, J.

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Biochemical evidence for a novel low molecular weight 2-5A-dependent RNase L in chronic fatigue syndrome von Suhadolnik, R J, Peterson, D L, O'Brien, K, Cheney, P R, Herst, C V, Reichenbach, N L, Kon, N, Horvath, S E, Iacono, K T, Adelson, M E, De Meirleir, K, De Becker, P, Charubala, R, Pfleiderer, W

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EPNS Newsletter, Editor L de Meirleir1More news from the board meeting in Southampton May 2001 von DEMEIRLEIR, L

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Generalized anxiety disorder in chronic fatigue syndrome von Fischler, B., Cluydts, R., De Gucht, V., Kaufman, L., De Meirleir, K.

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EPNS NewsletterMORE EPNS NEWS AFTER THE SOUTHAMPTON BOARD MEETING 11–12 May 2001 von DEMEIRLEIR, L

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EPNS NewsletterGUIDELINES AND PROCEDURES FOR APPLICATIONS TO HOST A SCIENTIFIC MEETING OF THE EPNS von DEMEIRLEIR, L

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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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A 90 MIN TIME TRIAL PERFORMANCE IS NOT INFLUENCED BY A 5-HT/NA REPUPTAKE INHIBITOR von Piacentini, M F., Buyse, L, Schutter, G De, Meeusen, R, DeMeirleir, K

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Pearson marrow pancreas syndrome: a molecular study and clinical management von Seneca, Sara, Meirleir, Linda De, Scbepper, Jean De, Balduck, Nadine, Jochmans, Kristin, Liebaers, Inge, Lissens, Willy

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A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis von Seneca, S., Abramowicz, M., Lissens, W., Muller, M. F., Vamos, E., Meirleir, L.

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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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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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YERSINIA PSEUDOTUBERCULOSIS SEPTICAEMIA IN THALASSAEMIA MAJOR von Gordts, B., Rummens, E., Demeirleir, L., Butzler, J.P.

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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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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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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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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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