P‐044: RETROSPECTIVE STUDY OF POST‐TRANSFUSION ALLOIMMUNIZATION IN THE SICKLE CELL POPULATION OF THE CHR CITADELLE von E., SEPULCHRE, J., MINON, H., PARIDAENS, V., STOJKOVIC, O., KETELSLEGERS, M., DRESSE

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Neonatal haemoglobinopathy screening in Belgium von Gulbis, B, Cotton, F, Ferster, A, Ketelslegers, O, Dresse, M F, Rongé-Collard, E, Minon, J M, Lé, P Q, Vertongen, F

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Inositide-specific phospholipase c β1 gene deletion is a rare event in myelodysplastic syndromes von Herens, C, Ketelslegers, O, Tassin, F, Hansen, S, Bours, V

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Reply to Lo Vasco et al von Herens, C, Ketelslegers, O, Tassin, F, Hansen, S, Bours, V

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Inositide-specific phospholipase c beta1 gene deletion is a rare event in myelodysplastic syndromes von Herens, C, Ketelslegers, O, Tassin, F, Hansen, S, Bours, V

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Infantile pyknocytosis: a rare form of neonatal hemolytic anemia. 5 case-studies von Limme, B, Dresse, M-F, Ketelslegers, O, Rigo, V, Hoyoux, C

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Neonatal screening improves sickle cell disease clinical outcome in Belgium von Lê, Phu-Quoc, Ferster, Alina, Dedeken, Laurence, Vermylen, Christiane, Vanderfaeillie, Anna, Rozen, Laurence, Heijmans, Catherine, Huybrechts, Sophie, Devalck, Christine, Cotton, Frédéric, Ketelslegers, Olivier, Dresse, Marie-Françoise, Fils, Jean-François, Gulbis, Béatrice

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La pyknocytose infantile : une anémie néonatale mal connue à propos de 5 cas von Limme, B., Dresse, M.-F., Ketelslegers, O., Rigo, V., Hoyoux, C.

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Inositide-specific phospholipase c b1 gene deletion is a rare event in myelodysplastic syndromes von Herens, C, Ketelslegers, O, Tassin, F, Hansen, S, Bours, V

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Inositide-specific phospholipase c 1 gene deletion is a rare event in myelodysplastic syndromes von Herens, C, Ketelslegers, O, Tassin, F, Hansen, S, Bours, V

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La pyknocytose infantile : une anémie néonatale mal connue à propos de 5cas von Limme, B., Dresse, M.-F., Ketelslegers, O., Rigo, V., Hoyoux, C.

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Sickle cell disease from Africa to Belgium, from neonatal screening to clinical management von Lê, Phu Quoc, Ferster, A, Cotton, F, Vertongen, F, Vermylen, C, Vanderfaeillie, A, Dedeken, L, Heijmans, C, Ketelslegers, O, Dresse, M F, Gulbis, B

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La pyknocytose infantile : une anemie neonatale mal connue a propos de 5cas von Limme, Boris, Dresse, Marie-Françoise, Ketelslegers, O., Rigo, Vincent, Hoyoux, Claire

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Neonatal haemoglobinpopathy screening in Belgium von Gulbis, B, Cotton, F, Ferster, A, Ketelslegers, O, DRESSE, Marie-Françoise, Rongé-Collard, E, Minon, JM, P Q, Lé, Vertongen, F

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Myostatin Gene Deletion Prevents Glucocorticoid-Induced Muscle Atrophy von Gilson, H, Schakman, O, Combaret, L, Lause, P, Grobet, L, Attaix, D, Ketelslegers, J. M, Thissen, J. P

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Insulin-Like Growth Factor-I Gene Transfer by Electroporation Prevents Skeletal Muscle Atrophy in Glucocorticoid-Treated Rats von Schakman, O, Gilson, H, de Coninck, V, Lause, P, Verniers, J, Havaux, X, Ketelslegers, J. M, Thissen, J. P

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Role of Akt/GSK-3β/β-Catenin Transduction Pathway in the Muscle Anti-Atrophy Action of Insulin-Like Growth Factor-I in Glucocorticoid-Treated Rats von Schakman, O, Kalista, S, Bertrand, L, Lause, P, Verniers, J, Ketelslegers, J. M, Thissen, J. P

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Sickle cell disease from Africa to Belgium, from neonatal screening to clinical management : SPECIAL DREPANOCYTOSE von LE PHU, Quoc, FERSTER, A, GULBIS, B, COTTON, F, VERTONGEN, F, VERMYLEN, C, VANDERFAEILLIE, A, DEDEKEN, L, HEIJMANS, C, KETELSLEGERS, O, DRESSE, M. F

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Superiority of big endothelin-1 and endothelin-1 over natriuretic peptides in predicting survival in severe congestive heart failure: a 7-year follow-up study von Van Beneden, Ronald, Gurné, Olivier, Selvais, Philippe L., Ahn, Sylvie A., Robert, Annie R., Ketelslegers, Jean-marie, Pouleur, Hubert G., Rousseau, Michel F.

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Cardiac natriuretic peptides for diagnosis and risk stratification in heart failure: influences of left ventricular dysfunction and coronary artery disease on cardiac hormonal acti... von SELVAIS, P. L, DONCKIER, J. E, ROBERT, A, LALOUX, O, VAN LINDEN, F, AHN, S, KETELSLEGERS, J. M, ROUSSEAU, M. F

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