Search Results - "VERMYLEN, C"

Contribution of plasma membrane lipid domains to red blood cell (re)shaping by Leonard, C., Conrard, L., Guthmann, M., Pollet, H., Carquin, M., Vermylen, C., Gailly, P., Van Der Smissen, P., Mingeot-Leclercq, M. P., Tyteca, D.

“…Although lipid domains have been evidenced in several living cell plasma membranes, their roles remain largely unclear. We here investigated whether they could…”
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Use of hydroxyurea from childhood to adult age in sickle cell disease: semen analysis by Lukusa, A K, Vermylen, C

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Multi-centre pilot study of 2-chlorodeoxyadenosine and cytosine arabinoside combined chemotherapy in refractory Langerhans cell histiocytosis with haematological dysfunction by Bernard, F., Thomas, C., Bertrand, Y., Munzer, M., Landman Parker, J., Ouache, M., Colin, V. Minard, Perel, Y., Chastagner, P., Vermylen, C., Donadieu, J.

“…The aim of this study was to assess the efficacy and adverse effects of 2-chlorodeoxyadenosine (2-CdA) and cytosine arabinoside (Ara-C) in children with…”
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Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International Registry by Zeidler, Cornelia, Grote, Ulrike A H, Nickel, Anna, Brand, Beate, Carlsson, Göran, Cortesão, Emília, Dufour, Carlo, Duhem, Caroline, Notheis, Gundula, Papadaki, Helen A, Tamary, Hannah, Tjønnfjord, Geir E, Tucci, Fabio, Van Droogenbroeck, Jan, Vermylen, Christiane, Voglova, Jaroslava, Xicoy, Blanca, Welte, Karl

“…Long-term granulocyte-colony stimulating factor treatment has been shown to be safe and effective in severe chronic neutropenia patients. However, data on its…”
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Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A by LANNOY, N., ABINET, I., BOSMANS, A., LAMBERT, C., VERMYLEN, C., HERMANS, C.

“…Haemophilia A (HA) is caused by widespread mutations in the factor VIII gene. The high spontaneous mutation rate of this gene means that roughly 40% of HA…”
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Ten years after the first inspection of a candidate European centre, an EBMT registry analysis suggests that clinical outcome is improved when hematopoietic SCT is performed in a JACIE accredited program by Chabannon, C, Pamphilon, D, Vermylen, C, Gratwohl, A, Niederwieser, D, McGrath, E, Lamers, C, Lanza, F, Slaper-Cortenbach, I, Madrigal, A, Apperley, J

“…In 2010, JACIE, the Joint Accreditation Committee of ISCT (International Society for Cell Therapy) Europe and EBMT (European group for Blood and Marrow…”
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Characterization of insulin resistance in young adult survivors of childhood acute lymphoblastic leukaemia and non-Hodgkin lymphoma by Beauloye, V, Vermylen, C, Maiter, D

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Hydroxyurea for Treatment of Severe Sickle Cell Anemia: A Pediatric Clinical Trial by Ferster, A., Vermylen, C., Cornu, G., Buyse, M., Corazza, F., Devalck, C., Fondu, P., Toppet, M., Sariban, E.

“…Hydroxyurea (HU) enhances the synthesis of fetal hemoglobin (HbF) and can improve the clinical course of some adult patients with sickle cell anemia (SCA). In…”
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Randomised revaccination with pneumococcal polysaccharide or conjugate vaccine in asplenic children previously vaccinated with polysaccharide vaccine by Smets, F, Bourgois, A, Vermylen, C, Brichard, B, Slacmuylders, P, Leyman, S, Sokal, E

“…Abstract Objective Asplenic children are at high risk of invasive pneumococcal infection. In this group, the American Academy of Pediatrics recommends a single…”
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Haematopoietic stem cell transplantation for sickle cell anaemia : the first 50 patients transplanted in belgium by VERMYLEN, C, CORNU, G, BEGUIN, Y, DRESSE, M, SARIBAN, E, FERSTER, A, BRICHARD, B, NINANE, J, FERRANT, A, ZENEBERGH, A, MAES, P, DHOOGE, C, BENOIT, Y

“…Fifty patients affected by sickle cell anaemia underwent transplantation of HLA-identical haematopoietic stem cells (bone marrow, 48; cord blood, 2). Two…”
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Outcome of 69 allogeneic stem cell transplantations for Fanconi anemia using HLA-matched unrelated donors : a study on behalf of the European Group for Blood and Marrow Transplantation by GUARDIOLA, P, PASQUINI, R, LJUNGMAN, P, MINIERO, R, SHAW, P. J, SOUILLET, G, MICHALLET, M, BEKASSY, A. N, KRIVAN, G, DI BARTOLOMEO, P, HEILMANN, C, ZANESCO, L, DOKAL, I, CAHN, J. Y, ARCESE, W, BACIGALUPO, A, GLUCKMAN, E, ORTEGA, J. J, VAN WEEL-SIPMAN, M, MARSH, J. C. W, BALL, S. E, LOCATELLI, F, VERMYLEN, C, SKINNER, R

“…Allogeneic stem cell transplantation is the only treatment that can restore a normal hematopoiesis in Fanconi anemia (FA). In this retrospective multicenter…”
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Successful hematopoietic stem cell transplantation in a child with active disseminated Mycobacterium fortuitum infection and interferon-gamma receptor 1 deficiency by Chantrain, C F, Bruwier, A, Brichard, B, Largent, V, Chapgier, A, Feinberg, J, Casanova, J-L, Stalens, J-P, Vermylen, C

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Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation by Zeidler, C., Welte, K., Barak, Y., Barriga, F., Bolyard, A.A., Boxer, L., Cornu, G., Cowan, M.J., Dale, D.C., Flood, T., Freedman, M., Gadner, H., Mandel, H., O'Reilly, R.J., Ramenghi, U., Reiter, A., Skinner, R., Vermylen, C., Levine, J.E.

“…Severe congenital neutropenia (CN) (Kostmann syndrome) is a hematologic disorder characterized by a maturation arrest of myelopoiesis at the…”
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Neonatal acute myeloid leukemia in an infant whose mother was exposed to diethylstilboestrol in utero by Chantrain, C.F., Sauvage, D., Brichard, B., Dupont, S., Poirel, H.A., Ameye, G., De Weer, A., Vandenberghe, P., Detaille, T., Anslot, C., de Cléty, S. Clément, Vermylen, C.

“…We report on an acute myeloid leukemia in a neonate whose mother was exposed to diethylstilboestrol in utero. The newborn presented with leukemia cutis,…”
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Inadvertent anticoagulation of a haemophiliac child with routine line flushing by LAMBERT, C., DENEYS, V., POTHEN, D., VERMYLEN, C., HERMANS, C.

“…We report the case of a 3‐year‐old boy with severe haemophilia A presenting with recurrent haemarthroses despite daily infusions of factor VIII delivered…”
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Shwachman-Diamond Syndrome: frequent misdiagnosis as Jeune Syndrome and other peculiarities by Meyts, I, Schaballie, H, Haerynck, F, Sevenants, L, Vermylen, C, Bordon, V, Bossuyt, X, Corveleyn, A, Uyttebroeck, A, Renard, M

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Evaluation of third-generation screening and confirmatory assays for HCV antibodies by Uyttendaele, S, Claeys, H, Mertens, W, Verhaert, H, Vermylen, C

“…A third-generation (gen.) screening and immunoblot assay (Ortho EIA-3.0; Chiron RIBA-3 prototype), using antigens derived from the capsid and different…”
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Persistence of fetal hemoglobin production after successful transplantation of cord blood stem cells in a patient with sickle cell anemia by Brichard, B., Vermylen, C., Ninane, J., Cornu, G.

“…A girl with sickle cell anemia was treated with cord blood transplantation combined with hematopoietic growth factor. Cord blood cells were collected from a…”
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A prospective study of minimal residual disease in childhood B‐lineage acute lymphoblastic leukaemia: MRD level at the end of induction is a strong predictive factor of relapse by Jacquy, C., Delepaut, B., Van Daele, S., Vaerman, J. L., Zenebergh, A., Brichard, B., Vermylen, C., Cornu, G., Martiat, P.

“…We prospectively investigated minimal residual disease (MRD) in 51 children with B‐lineage acute lymphoblastic leukaemia (ALL) treated according to the Fralle…”
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Long-Term Follow-up of Residual Disease in Acute Lymphoblastic Leukemia Patients in Complete Remission Using Clonogeneic IgH Probes and the Polymerase Chain Reaction by Nizet, Y., Van Daele, S., Lewalle, P., Vaerman, J.L., Philippe, M., Vermylen, C., Cornu, G., Ferrant, A., Michaux, J.L., Martiat, P.

“…We sequentially studied bone marrow (BM) samples of 25 patients in complete remission of an acute lymphoblastic leukemia (ALL) using a simplified polymerase…”
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