Antitumor activity of an immunocytokine composed of an anti-GD2 antibody and the IL-15 superagonist RLI

por Vincent, Marie, Quéméner, Agnès, Jacques, Yannick
Publicado 2013

Fatal lactic acidosis possibly related to ganciclovir therapy in a renal transplant patient?

por Wittebole, Xavier, Morelle, Johann, Vincent, Marie-Françoise, Hantson, Philippe
Publicado 2015

Macrophage Mitochondrial Biogenesis and Metabolic Reprogramming Induced by Leishmania donovani Require Lipophosphoglycan and Type I Interferon Signaling

por Acevedo Ospina, Hamlet, Guay-Vincent, Marie-Michèle, Descoteaux, Albert
Publicado 2022

Three patients presenting with severe macrosomia and congenital hypertrophic cardiomyopathy: a case series

por Vincent, Marie, Benbrik, Nadir, Romefort, Bénédicte, Colombel, Agnès, Bézieau, Stéphane, Isidor, Bertrand
Publicado 2017

Fatal Idiopathic Hyperammonemia after Induction Chemotherapy for Acute Myeloid Leukemia

por Angelo, Christophe, Vincent, Marie-Françoise, Komuta, Mina, Hantson, Philippe, Straetmans, Nicole, Boulet, Edwige
Publicado 2020

Hyperammonemic Encephalopathy and Lipid Dysmetabolism in a Critically Ill Patient After a Short Course of Amiodarone

por Cappe, Maximilien, Hantson, Philippe, Komuta, Mina, Vincent, Marie-Françoise, Laterre, Pierre-François, Ould-Nana, Ismaïl
Publicado 2019

Revisiting Leishmania GP63 host cell targets reveals a limited spectrum of substrates

por Guay-Vincent, Marie-Michèle, Matte, Christine, Berthiaume, Anne-Marie, Olivier, Martin, Jaramillo, Maritza, Descoteaux, Albert
Publicado 2022

A self‐portrait: Design opportunities for a tool that supports children's involvement in brain‐related health care

por Meulendijks, Paul, van Haren, Neeltje E. M., Gielen, Mathieu A., van Veelen‐Vincent, Marie‐Lise C.
Publicado 2022

Extreme Maternal Metabolic Acidosis Leading to Fetal Distress and Emergency Caesarean Section

por Cecere, Nicolas, Hubinont, Corinne, Kabulu Kadingi, Arnauld, Vincent, Marie-Françoise, Van den Bergh, Peter, Onnela, Anna, Hantson, Philippe
Publicado 2013

Identification of Mutations in SDR9C7 in Three Patients with Autosomal Recessive Congenital Ichthyosis

por MAZEREEUW-HAUTIER, Juliette, SEVERINO-FREIRE, Maella, GASTON, Véronique, TEXIER, Hélène, VINCENT, Marie, AUBERT, Hélène, MORICE-PICARD, Fanny, JONCA, Nathalie
Publicado 2020

A Mouse Model of L-2-Hydroxyglutaric Aciduria, a Disorder of Metabolite Repair

por Rzem, Rim, Achouri, Younes, Marbaix, Etienne, Schakman, Olivier, Wiame, Elsa, Marie, Sandrine, Gailly, Philippe, Vincent, Marie-Françoise, Veiga-da-Cunha, Maria, Van Schaftingen, Emile
Publicado 2015

Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications

por Myers, Lynnea, Blyth, Moira, Moradkhani, Kamran, Hranilović, Dubravka, Polesie, Sam, Isaksson, Johan, Nordgren, Ann, Bucan, Maja, Vincent, Marie, Bölte, Sven, Anderlid, Britt‐Marie, Tammimies, Kristiina
Publicado 2019

Evolutionary conserved NSL complex/BRD4 axis controls transcription activation via histone acetylation

por Gaub, Aline, Sheikh, Bilal N., Basilicata, M. Felicia, Vincent, Marie, Nizon, Mathilde, Colson, Cindy, Bird, Matthew J., Bradner, James E., Thevenon, Julien, Boutros, Michael, Akhtar, Asifa
Publicado 2020

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

por Redin, Claire, Le Gras, Stéphanie, Mhamdi, Oussema, Geoffroy, Véronique, Stoetzel, Corinne, Vincent, Marie-Claire, Chiurazzi, Pietro, Lacombe, Didier, Ouertani, Ines, Petit, Florence, Till, Marianne, Verloes, Alain, Jost, Bernard, Chaabouni, Habiba Bouhamed, Dollfus, Helene, Mandel, Jean-Louis, Muller, Jean
Publicado 2012

Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes

por Begemann, Anaïs, Acuña, Mario A., Zweier, Markus, Vincent, Marie, Steindl, Katharina, Bachmann-Gagescu, Ruxandra, Hackenberg, Annette, Abela, Lucia, Plecko, Barbara, Kroell-Seger, Judith, Baumer, Alessandra, Yamakawa, Kazuhiro, Inoue, Yushi, Asadollahi, Reza, Sticht, Heinrich, Zeilhofer, Hanns Ulrich, Rauch, Anita
Publicado 2019

Neonatal Thyroid-Stimulating Hormone Concentrations in Belgium: A Useful Indicator for Detecting Mild Iodine Deficiency?

por Vandevijvere, Stefanie, Coucke, Wim, Vanderpas, Jean, Trumpff, Caroline, Fauvart, Maarten, Meulemans, Ann, Marie, Sandrine, Vincent, Marie-Françoise, Schoos, Roland, Boemer, François, Vanwynsberghe, Timothy, Philips, Eddy, Eyskens, François, Wuyts, Brigitte, Selimaj, Valbona, Van Overmeire, Bart, Kirkpatrick, Christine, Van Oyen, Herman, Moreno-Reyes, Rodrigo
Publicado 2012

Craniosynostosis affects the majority of mucopolysaccharidosis patients and can contribute to increased intracranial pressure

por Oussoren, Esmee, Mathijssen, Irene M. J., Wagenmakers, Margreet, Verdijk, Rob M., Bredero-Boelhouwer, Hansje H., van Veelen-Vincent, Marie-Lise C., van der Meijden, Jan C., van den Hout, Johanna M. P., Ruijter, George J. G., van der Ploeg, Ans T., Langeveld, Mirjam
Publicado 2018

Belgian rare diseases plan in clinical pathology: identification of key biochemical diagnostic tests and establishment of reference laboratories and financing conditions

por Vandevelde, Nathalie M., Vermeersch, Pieter, Devreese, Katrien M. J., Vincent, Marie-Françoise, Gulbis, Béatrice, Eyskens, François, Boemer, François, Gothot, André, Van Hoof, Viviane O., Bonroy, Carolien, Stepman, Hedwig, Martens, Geert A., Bossuyt, Xavier, Roosens, Laurence, Smet, Julie, Laeremans, Hilde, Weets, Ilse, Minon, Jean-Marc, Vernelen, Kris, Coucke, Wim
Publicado 2021

Treatment of two infants with PIK3CA-related overgrowth spectrum by alpelisib

por Morin, Gabriel, Degrugillier-Chopinet, Caroline, Vincent, Marie, Fraissenon, Antoine, Aubert, Hélène, Chapelle, Célia, Hoguin, Clément, Dubos, François, Catteau, Benoit, Petit, Florence, Mezel, Aurélie, Domanski, Olivia, Herbreteau, Guillaume, Alesandrini, Marie, Boddaert, Nathalie, Boutry, Nathalie, Broissand, Christine, Han, Tianxiang Kevin, Branle, Fabrice, Sarnacki, Sabine, Blanc, Thomas, Guibaud, Laurent, Canaud, Guillaume
Publicado 2022

The clinical significance of small copy number variants in neurodevelopmental disorders

por Asadollahi, Reza, Oneda, Beatrice, Joset, Pascal, Azzarello-Burri, Silvia, Bartholdi, Deborah, Steindl, Katharina, Vincent, Marie, Cobilanschi, Joana, Sticht, Heinrich, Baldinger, Rosa, Reissmann, Regina, Sudholt, Irene, Thiel, Christian T, Ekici, Arif B, Reis, André, Bijlsma, Emilia K, Andrieux, Joris, Dieux, Anne, FitzPatrick, David, Ritter, Susanne, Baumer, Alessandra, Latal, Beatrice, Plecko, Barbara, Jenni, Oskar G, Rauch, Anita
Publicado 2014