Thrombophilic Factors Do Not Predict Outcomes in Renal Transplant Recipients Under Prophylactic Acetylsalicylic Acid von Ghisdal, L., Broeders, N., Wissing, K.‐M., Saidi, A., Bensalem, T., Mbaba Mena, J., Lemy, A., Wijns, W., Pradier, O., Hoang, A.‐D., Mikhalski, D., Donckier, V., Cochaux, P., El Housni, H., Abramowicz, M., Vereerstraeten, P., Abramowicz, D.

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Chorioretinal post-transplant lymphoproliferative disorder induced by the Epstein-Barr virus von Demols, P F, Cochaux, P M, Velu, T, Caspers-Velu, L

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Relative contribution of Ki-ras gene analysis and brush cytology during ERCP for the diagnosis of biliary and pancreatic diseases von Van Laethem, Jean-Luc, Bourgeois, Vincent, Parma, Jasmine, Delhaye, Myriam, Cochaux, Pascale, Velu, Thierry, Devière, Jacques, Cremer, Michel

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ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia von CAVE, H, CACHEUX, V, RAYNAUD, S, BRUNIE, G, BAKKUS, M, COCHAUX, P, PREUDHOMME, C, LAÏ, J. L, VILMER, E, GRANDCHAMP, B

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Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter von ABRAMOWICZ, M. J, TARGOVNIK, H. M, VARELA, V, COCHAUX, P, KRAWIEC, L, PISAREV, M. A, PROPATO, F. V. E, JUVENAL, G, CHESTER, H. A, VASSART, G

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A rare variant, I852M, of the RET proto-oncogene in a patient with medullary thyroid carcinoma at age 20 years von Demeester, Rémy, Parma, Jasmine, Cochaux, Pascale, Vassart, Gilbert, Abramowicz, Marc J.

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Absence of Epstein-Barr virus in medullary carcinoma of the breast as demonstrated by immunophenotyping, in situ hybridization and polymerase chain reaction von LESPAGNARD, L, COCHAUX, P, LARSIMONT, D, DEGEYTER, M, VELU, T, HEIMANN, R

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Systemic responsiveness to lipopolysaccharide and polymorphisms in the toll-like receptor 4 gene in human beings von Michel, Olivier, LeVan, Tricia D, Stern, Debbie, Dentener, Mieke, Thorn, Jörgen, Gnat, Daniele, Beijer, M.Lena, Cochaux, Pascale, Holt, Patrick G, Martinez, Fernando D, Rylander, Ragnar

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Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas von Parma, Jasmine, Duprez, Laurence, Sande, Jacqueline Van, Cochaux, Pascale, Gervy, Christine, Mockel, Jean, Dumont, Jacques, Vassart, Gilbert

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The Δccr5 Mutation Conferring Protection Against HIV-1 in Caucasian Populations Has a Single and Recent Origin in Northeastern Europe von Libert, Frédérick, Cochaux, Pascale, Beckman, Gunhild, Samson, Michel, Aksenova, Marina, Cao, Antonio, Czeizel, Andrew, Claustres, Mireille, de la Rúa, Concepción, Ferrari, Maurizio, Ferrec, Claude, Glover, Guillermo, Grinde, Bjorn, Güran, Sefik, Kucinskas, Vaidutis, Lavinha, Joao, Mercier, Bernard, Ogur, Gönül, Peltonen, Leena, Rosatelli, Cristina, Schwartz, Marianne, Spitsyn, Victor, Timar, Laszlo, Beckman, Lars, Parmentier, Marc, Vassart, Gilbert

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Clonal Proliferation of Type 2 Helper T Cells in a Man with the Hypereosinophilic Syndrome von Cogan, Elie, Schandene, Liliane, Crusiaux, Alain, Cochaux, Pascale, Velu, Thierry, Goldman, Michel

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Brief report: clonal proliferation of type 2 helper T cells in a man with the hypereosinophilic syndrome von Cogan, E, Schandené, L, Crusiaux, A, Cochaux, P, Velu, T, Goldman, M

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Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy von Obermaier-Kusser, B, Lorenz, B, Schubring, S, Paprotta, A, Zerres, K, Meitinger, T, Meire, F, Cochaux, P, Blankenagel, A, Kommerell, G

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Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations von Estivill, Xavier, Bancells, Consol, Ramos, Cristina

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Disseminated angiosarcoma presenting as a hemophagocytic syndrome in a renal allograft recipient von Dargent, J.‐L., Vermylen, P., Abramowicz, D., Lespagnard, L., Cochaux, P., Capel, P., Velu, T., Vereerstraeten, P., Haot, J., Wolf‐Peeters, C. De

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Pernicious anaemia and hypoparathyroidism in a patient with Kearns‐Sayre syndrome with mitochondrial DNA duplication von Abramowicz, M. J., Cochaux, P., Cohen, L. H. F., Vamos, E.

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Hb Ube-2 [α68(E17)Asn→Asp] and Hb Hafnia [β116(G18)His→Gln] Observed During Neonatal Screening in Brussels von Cotton, F., Hanstn, V., Lin, C., Parma, J., Cochaux, P., Damis, E., Vertongen, F., Gulbis, B.

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Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations von Meire, F. M., Candaele, C., Van Coster, R., Cochaux, P., Obermaier-Kusser, B., Martin, J.-J.

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Morphologic and phenotypic changes of the leukemic cells in a case of marginal zone B-cell lymphoma von DARGENT, J. L, DELVILLE, J. P, KORNREICH, A, PRADIER, O, COCHAUX, P, VELU, T, CAPEL, P, FEREMANS, W, NEVE, P

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A mechanism in the control of intracellular cAMP level: the activation of a calmodulin-sensitive phosphodiesterase by a rise of intracellular free calcium von Erneux, C., Van Sande, J., Miot, F., Cochaux, P., Decoster, C., Dumont, J.E.

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