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

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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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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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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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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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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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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-like syndrome in organic aciduria von Blecker, U, De Meirleir, L, De Raeve, L, Ramet, J, Vandenplas, Y

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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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Isolation of a full-length complementary DNA coding for human E1 alpha subunit of the pyruvate dehydrogenase complex von De Meirleir, L, MacKay, N, Lam Hon Wah, A M, Robinson, B H

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E1 pyruvate dehydrogenase deficiency in a child with motor neuropathy von BONNE, G, BENELLI, C, MARSAC, C, DE MEIRLEIR, L, LISSENS, W, CHAUSSAIN, M, DIRY, M, CLOT, J.-P, PONSOT, G, GEOFFROY, V, LEROUX, J.-P

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Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathy von Tein, I, De Vivo, D C, Bierman, F, Pulver, P, De Meirleir, L J, Cvitanovic-Sojat, L, Pagon, R A, Bertini, E, Dionisi-Vici, C, Servidei, S

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