Is There Any Improvement of the Coagulation Imbalance in Sickle Cell Disease after Hematopoietic Stem Cell Transplantation?

di Rozen, Laurence, Noubouossie, Denis F., Dedeken, Laurence, Lê, Phu Quoc, Ferster, Alina, Demulder, Anne
Pubblicato in J Clin Med (2019)

Detection of Herpesviridae in Whole Blood by Multiplex PCR DNA-Based Microarray Analysis after Hematopoietic Stem Cell Transplantation

di Debaugnies, France, Busson, Laurent, Ferster, Alina, Lewalle, Philippe, Azzi, Nadira, Aoun, Mickael, Verhaegen, Godelieve, Mahadeb, Bhavna, de Marchin, Jérôme, Vandenberg, Olivier, Hallin, Marie
Pubblicazione 2014

Reduced recruitment of 53BP1 during interstrand crosslink repair is associated with genetically inherited attenuation of mitomycin C sensitivity in a family with Fanconi anemia

di Lesport, Emilie, Ferster, Alina, Biver, Armand, Roch, Benoit, Vasquez, Nadia, Jabado, Nada, Vives, Francina Langa, Revy, Patrick, Soulier, Jean, de Villartay, Jean-Pierre
Pubblicato in Oncotarget (2017)

Serum calprotectin (S100A8/A9): a promising biomarker in diagnosis and follow-up in different subgroups of juvenile idiopathic arthritis

di La, Céline, Lê, Phu Quoc, Ferster, Alina, Goffin, Laurence, Spruyt, Delphine, Lauwerys, Bernard, Durez, Patrick, Boulanger, Cecile, Sokolova, Tatiana, Rasschaert, Joanne, Badot, Valérie
Pubblicato in RMD Open (2021)

Neonatal Screening for Sickle Cell Disease in Belgium for More than 20 Years: An Experience for Comprehensive Care Improvement

di Gulbis, Béatrice, Lê, Phu-Quoc, Ketelslegers, Olivier, Dresse, Marie-Françoise, Adam, Anne-Sophie, Cotton, Frédéric, Boemer, François, Bours, Vincent, Minon, Jean-Marc, Ferster, Alina
Pubblicato in Int J Neonatal Screen (2018)

Reduction of the Six-Minute Walk Distance in Children with Sickle Cell Disease Is Correlated with Silent Infarct: Results from a Cross-Sectional Evaluation in a Single Center in Be...

di Dedeken, Laurence, Chapusette, Rudy, Lê, Phu Quoc, Heijmans, Catherine, Devalck, Christine, Huybrechts, Sophie, Ziereisen, France, Hanssens, Laurence, Rozen, Laurence, Noubouossie, Denis, Mujinga, Malou Ngalula, Ferster, Alina
Pubblicazione 2014

Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency

di Veiga-da-Cunha, Maria, Chevalier, Nathalie, Stephenne, Xavier, Defour, Jean-Philippe, Paczia, Nicole, Ferster, Alina, Achouri, Younes, Dewulf, Joseph P., Linster, Carole L., Bommer, Guido T., Van Schaftingen, Emile
Pubblicato in Proc Natl Acad Sci U S A (2019)

CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency

di van Zelm, Menno C., Smet, Julie, Adams, Brigitte, Mascart, Françoise, Schandené, Liliane, Janssen, Françoise, Ferster, Alina, Kuo, Chiung-Chi, Levy, Shoshana, van Dongen, Jacques J.M., van der Burg, Mirjam
Pubblicazione 2010

Malignancies after hematopoietic cell transplantation for primary immune deficiencies: a report from the Center for International Blood and Marrow Transplant Research

di Kamani, Naynesh R., Kumar, Shimareet, Hassebroek, Anna, Eapen, Mary, LeRademacher, Jennifer, Casper, James, Cowan, Morton, de Toledo, José Sánchez, Ferster, Alina, Szabolcs, Paul, Wingard, John R., Horwitz, Edwin, Filipovich, Alexandra H.
Pubblicazione 2011

Dexamethasone (6 mg/m(2)/day) and prednisolone (60 mg/m(2)/day) were equally effective as induction therapy for childhood acute lymphoblastic leukemia in the EORTC CLG 58951 random...

di Domenech, Carine, Suciu, Stefan, De Moerloose, Barbara, Mazingue, Françoise, Plat, Geneviève, Ferster, Alina, Uyttebroeck, Anne, Sirvent, Nicolas, Lutz, Patrick, Yakouben, Karima, Munzer, Martine, Röhrlich, Pierre, Plantaz, Dominique, Millot, Frederic, Philippet, Pierre, Dastugue, Nicole, Girard, Sandrine, Cavé, Hélène, Benoit, Yves, Bertrandfor, Yves
Pubblicazione 2014

Unique long non-coding RNA expression signature in ETV6/RUNX1-driven B-cell precursor acute lymphoblastic leukemia

di Ghazavi, Farzaneh, Moerloose, Barbara De, Loocke, Wouter Van, Wallaert, Annelynn, Helsmoortel, Hetty H., Ferster, Alina, Bakkus, Marleen, Plat, Geneviève, Delabesse, Eric, Uyttebroeck, Anne, Nieuwerburgh, Filip Van, Deforce, Dieter, Roy, Nadine Van, Speleman, Frank, Benoit, Yves, Lammens, Tim, Vlierberghe, Pieter Van
Pubblicato in Oncotarget (2016)

Prolonged versus standard native E. coli asparaginase therapy in childhood acute lymphoblastic leukemia and non-Hodgkin lymphoma: final results of the EORTC-CLG randomized phase II...

di Mondelaers, Veerle, Suciu, Stefan, De Moerloose, Barbara, Ferster, Alina, Mazingue, Françoise, Plat, Geneviève, Yakouben, Karima, Uyttebroeck, Anne, Lutz, Patrick, Costa, Vitor, Sirvent, Nicolas, Plouvier, Emmanuel, Munzer, Martine, Poirée, Maryline, Minckes, Odile, Millot, Frédéric, Plantaz, Dominique, Maes, Philip, Hoyoux, Claire, Cavé, Hélène, Rohrlich, Pierre, Bertrand, Yves, Benoit, Yves
Pubblicato in Haematologica (2017)

Favorable outcomes of hematopoietic stem cell transplantation in children and adolescents with Diamond-Blackfan anemia

di Strahm, Brigitte, Loewecke, Felicia, Niemeyer, Charlotte M., Albert, Michael, Ansari, Marc, Bader, Peter, Bertrand, Yves, Burkhardt, Birgit, Da Costa, Lydie M., Ferster, Alina, Fischer, Alexandra, Güngör, Tayfun, Gruhn, Bernd, Hainmann, Ina, Kapp, Friedrich, Lang, Peter, Müller, Ingo, Schulz, Ansgar, Szvetnik, Amina, Wlodarski, Marcin, Noellke, Peter, Leblanc, Thierry, Dalle, Jean-Hugues
Pubblicato in Blood Adv (2020)

Human adenylate kinase 2 deficiency causes a profound haematopoietic defect associated with sensorineural deafness

di Lagresle-Peyrou, Chantal, Six, Emmanuelle M., Picard, Capucine, Rieux-Laucat, Frédéric, Michel, Vincent, Ditadi, Andrea, Chappedelaine, Corinne Demerens-de, Morillon, Estelle, Valensi, Françoise, Simon-Stoos, Karen L., Mullikin, James C., Noroski, Lenora M., Besse, Céline, Wulffraat, Nicolas M., Ferster, Alina, Abecasis, Manuel M., Calvo, Fabien, Petit, Christine, Candotti, Fabio, Abel, Laurent, Fischer, Alain, Cavazzana-Calvo, Marina
Pubblicazione 2008

CD200/BTLA deletions in pediatric precursor B-cell acute lymphoblastic leukemia treated according to the EORTC-CLG 58951 protocol

di Ghazavi, Farzaneh, Clappier, Emmanuelle, Lammens, Tim, Suciu, Stefan, Caye, Aurélie, Zegrari, Samira, Bakkus, Marleen, Grardel, Nathalie, Benoit, Yves, Bertrand, Yves, Minckes, Odile, Costa, Vitor, Ferster, Alina, Mazingue, Françoise, Plat, Geneviève, Plouvier, Emmanuel, Poirée, Marilyne, Uyttebroeck, Anne, van der Werff-ten Bosch, Jutte, Yakouben, Karima, Helsmoortel, Hetty, Meul, Magali, Van Roy, Nadine, Philippé, Jan, Speleman, Frank, Cavé, Hélène, Van Vlierberghe, Pieter, De Moerloose, Barbara
Pubblicato in Haematologica (2015)

Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects

di Weemaes, Corry MR, van Tol, Maarten JD, Wang, Jun, van Ostaijen-ten Dam, Monique M, van Eggermond, Marja CJA, Thijssen, Peter E, Aytekin, Caner, Brunetti-Pierri, Nicola, van der Burg, Mirjam, Graham Davies, E, Ferster, Alina, Furthner, Dieter, Gimelli, Giorgio, Gennery, Andy, Kloeckener-Gruissem, Barbara, Meyn, Stephan, Powell, Cynthia, Reisli, Ismail, Schuetz, Catharina, Schulz, Ansgar, Shugar, Andrea, van den Elsen, Peter J, van der Maarel, Silvère M
Pubblicazione 2013

Clinical Implications of Minimal Residual Disease Detection in Infants With KMT2A-Rearranged Acute Lymphoblastic Leukemia Treated on the Interfant-06 Protocol

di Stutterheim, Janine, van der Sluis, Inge M., de Lorenzo, Paola, Alten, Julia, Ancliffe, Philip, Attarbaschi, Andishe, Brethon, Benoit, Biondi, Andrea, Campbell, Myriam, Cazzaniga, Giovanni, Escherich, Gabriele, Ferster, Alina, Kotecha, Rishi S., Lausen, Birgitte, Li, Chi Kong, Lo Nigro, Luca, Locatelli, Franco, Marschalek, Rolf, Meyer, Claus, Schrappe, Martin, Stary, Jan, Vora, Ajay, Zuna, Jan, van der Velden, Vincent H. J., Szczepanski, Tomasz, Valsecchi, Maria Grazia, Pieters, Rob
Pubblicato in J Clin Oncol (2021)

Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2

di de Greef, Jessica C., Wang, Jun, Balog, Judit, den Dunnen, Johan T., Frants, Rune R., Straasheijm, Kirsten R., Aytekin, Caner, van der Burg, Mirjam, Duprez, Laurence, Ferster, Alina, Gennery, Andrew R., Gimelli, Giorgio, Reisli, Ismail, Schuetz, Catharina, Schulz, Ansgar, Smeets, Dominique F.C.M., Sznajer, Yves, Wijmenga, Cisca, van Eggermond, Marja C., van Ostaijen-ten Dam, Monique M., Lankester, Arjan C., van Tol, Maarten J.D., van den Elsen, Peter J., Weemaes, Corry M., van der Maarel, Silvère M.
Pubblicazione 2011

Sickle cell disease: an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation

di Gluckman, Eliane, Cappelli, Barbara, Bernaudin, Francoise, Labopin, Myriam, Volt, Fernanda, Carreras, Jeanette, Pinto Simões, Belinda, Ferster, Alina, Dupont, Sophie, de la Fuente, Josu, Dalle, Jean-Hugues, Zecca, Marco, Walters, Mark C., Krishnamurti, Lakshmanan, Bhatia, Monica, Leung, Kathryn, Yanik, Gregory, Kurtzberg, Joanne, Dhedin, Nathalie, Kuentz, Mathieu, Michel, Gerard, Apperley, Jane, Lutz, Patrick, Neven, Bénédicte, Bertrand, Yves, Vannier, Jean Pierre, Ayas, Mouhab, Cavazzana, Marina, Matthes-Martin, Susanne, Rocha, Vanderson, Elayoubi, Hanadi, Kenzey, Chantal, Bader, Peter, Locatelli, Franco, Ruggeri, Annalisa, Eapen, Mary
Pubblicato in Blood (2017)

Risk factors and outcomes according to age at transplantation with an HLA-identical sibling for sickle cell disease

di Cappelli, Barbara, Volt, Fernanda, Tozatto-Maio, Karina, Scigliuolo, Graziana Maria, Ferster, Alina, Dupont, Sophie, Simões, Belinda Pinto, Al-Seraihy, Amal, Aljurf, Mahmoud D., Almohareb, Fahad, Belendez, Cristina, Matthes, Susanne, Dhedin, Nathalie, Pondarre, Corinne, Dalle, Jean-Hugues, Bertrand, Yves, Vannier, Jean Pierre, Kuentz, Mathieu, Lutz, Patrick, Michel, Gérard, Rafii, Hanadi, Neven, Benedicte, Zecca, Marco, Bader, Peter, Cavazzana, Marina, Labopin, Myriam, Locatelli, Franco, Magnani, Alessandra, Ruggeri, Annalisa, Rocha, Vanderson, Bernaudin, Françoise, de La Fuente, Josu, Corbacioglu, Selim, Gluckman, Eliane
Pubblicato in Haematologica (2019)