Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe

por Cardenal‐Muñoz, Elena, Auvin, Stéphane, Villanueva, Vicente, Cross, J. Helen, Zuberi, Sameer M., Lagae, Lieven, Aibar, José Ángel
Publicado 2021

Development of nanostars as a biocompatible tumor contrast agent: toward in vivo SERS imaging

por D’Hollander, Antoine, Mathieu, Evelien, Jans, Hilde, Vande Velde, Greetje, Stakenborg, Tim, Van Dorpe, Pol, Himmelreich, Uwe, Lagae, Liesbet
Publicado 2016

Accurate label-free 3-part leukocyte recognition with single cell lens-free imaging flow cytometry

por Li, Yuqian, Cornelis, Bruno, Dusa, Alexandra, Vanmeerbeeck, Geert, Vercruysse, Dries, Sohn, Erik, Blaszkiewicz, Kamil, Prodanov, Dimiter, Schelkens, Peter, Lagae, Liesbet
Publicado 2018

PPFIA4 mutation: A second hit in POLG related disease?

por Sourbron, Jo, Jansen, Katrien, Aerts, Nele, Lagae, Lieven
Publicado 2021

Author Correction: Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment

por Mills, James D., Iyer, Anand M., van Scheppingen, Jackelien, Bongaarts, Anika, Anink, Jasper J., Janssen, Bart, Zimmer, Till S., Spliet, Wim G., van Rijen, Peter C., Jansen, Floor E., Feucht, Martha, Hainfellner, Johannes A., Krsek, Pavel, Zamecnik, Josef, Kotulska, Katarzyna, Jozwiak, Sergiusz, Jansen, Anna, Lagae, Lieven, Curatolo, Paolo, Kwiatkowski, David J., Pasterkamp, R. Jeroen, Senthilkumar, Ketharini, von Oerthel, Lars, Hoekman, Marco F., Gorter, Jan A., Crino, Peter B., Mühlebner, Angelika, Scicluna, Brendon P., Aronica, Eleonora
Publicado 2022

Photoresistance Switching of Plasmonic Nanopores

por Li, Yi, Nicoli, Francesca, Chen, Chang, Lagae, Liesbet, Groeseneken, Guido, Stakenborg, Tim, Zandbergen, Henny W., Dekker, Cees, Van Dorpe, Pol, Jonsson, Magnus P.
Publicado 2014

Long-term accelerometry-triggered video monitoring and detection of tonic–clonic and clonic seizures in a home environment: Pilot study

por Van de Vel, Anouk, Milosevic, Milica, Bonroy, Bert, Cuppens, Kris, Lagae, Lieven, Vanrumste, Bart, Van Huffel, Sabine, Ceulemans, Berten
Publicado 2016

Drug repurposing for Dravet syndrome in scn1Lab (−/−) mutant zebrafish

por Sourbron, Jo, Partoens, Michèle, Scheldeman, Chloë, Zhang, Yifan, Lagae, Lieven, de Witte, Peter
Publicado 2019

Use of Zebrafish Models to Boost Research in Rare Genetic Diseases

por Crouzier, Lucie, Richard, Elodie M., Sourbron, Jo, Lagae, Lieven, Maurice, Tangui, Delprat, Benjamin
Publicado 2021

Less is more: Antibiotics at the beginning of life

por Stocker, Martin, Klingenberg, Claus, Navér, Lars, Nordberg, Viveka, Berardi, Alberto, el Helou, Salhab, Fusch, Gerhard, Bliss, Joseph M., Lehnick, Dirk, Dimopoulou, Varvara, Guerina, Nicholas, Seliga-Siwecka, Joanna, Maton, Pierre, Lagae, Donatienne, Mari, Judit, Janota, Jan, Agyeman, Philipp K. A., Pfister, Riccardo, Latorre, Giuseppe, Maffei, Gianfranco, Laforgia, Nichola, Mózes, Enikő, Størdal, Ketil, Strunk, Tobias, Giannoni, Eric
Publicado 2023

Altered functional connectivity of the language network in ASD: Role of classical language areas and cerebellum()

por Verly, Marjolein, Verhoeven, Judith, Zink, Inge, Mantini, Dante, Peeters, Ronald, Deprez, Sabine, Emsell, Louise, Boets, Bart, Noens, Ilse, Steyaert, Jean, Lagae, Lieven, De Cock, Paul, Rommel, Nathalie, Sunaert, Stefan
Publicado 2014

Ion Current Rectification, Limiting and Overlimiting Conductances in Nanopores

por van Oeffelen, Liesbeth, Van Roy, Willem, Idrissi, Hosni, Charlier, Daniel, Lagae, Liesbet, Borghs, Gustaaf
Publicado 2015

High spatial resolution nanoslit SERS for single-molecule nucleobase sensing

por Chen, Chang, Li, Yi, Kerman, Sarp, Neutens, Pieter, Willems, Kherim, Cornelissen, Sven, Lagae, Liesbet, Stakenborg, Tim, Van Dorpe, Pol
Publicado 2018

The importance of clinician, patient and researcher collaborations in Alport syndrome

por Rheault, Michelle N., Savige, Judith, Randles, Michael J., Weinstock, André, Stepney, Melissa, Turner, A Neil, Parziale, Gina, Gross, Oliver, Flinter, Frances A, Miner, Jeffrey H, Lagas, Sharon, Gear, Susie, Lennon, Rachel
Publicado 2019

miRNAs and isomiRs: Serum-Based Biomarkers for the Development of Intellectual Disability and Autism Spectrum Disorder in Tuberous Sclerosis Complex

por Scheper, Mirte, Romagnolo, Alessia, Besharat, Zein Mersini, Iyer, Anand M., Moavero, Romina, Hertzberg, Christoph, Weschke, Bernhard, Riney, Kate, Feucht, Martha, Scholl, Theresa, Petrak, Borivoj, Maulisova, Alice, Nabbout, Rima, Jansen, Anna C., Jansen, Floor E., Lagae, Lieven, Urbanska, Malgorzata, Ferretti, Elisabetta, Tempes, Aleksandra, Blazejczyk, Magdalena, Jaworski, Jacek, Kwiatkowski, David J., Jozwiak, Sergiusz, Kotulska, Katarzyna, Sadowski, Krzysztof, Borkowska, Julita, Curatolo, Paolo, Mills, James D., Aronica, Eleonora
Publicado 2022

Oral co-administration of elacridar and ritonavir enhances plasma levels of oral paclitaxel and docetaxel without affecting relative brain accumulation

por Hendrikx, J J M A, Lagas, J S, Wagenaar, E, Rosing, H, Schellens, J H M, Beijnen, J H, Schinkel, A H
Publicado 2014

The 2014 International Workshop on Alport Syndrome

por Miner, Jeffrey H, Baigent, Colin, Flinter, Frances, Gross, Oliver, Judge, Parminder, Kashtan, Clifford E, Lagas, Sharon, Savige, Judith, Blatt, Dave, Ding, Jie, Gale, Daniel P, Midgley, Julian P, Povey, Sue, Prunotto, Marco, Renault, Daniel, Skelding, Jules, Turner, A Neil, Gear, Susie
Publicado 2014

Pharmacological Characterization of an Antisense Knockdown Zebrafish Model of Dravet Syndrome: Inhibition of Epileptic Seizures by the Serotonin Agonist Fenfluramine

por Zhang, Yifan, Kecskés, Angéla, Copmans, Daniëlle, Langlois, Mélanie, Crawford, Alexander D., Ceulemans, Berten, Lagae, Lieven, de Witte, Peter A. M., Esguerra, Camila V.
Publicado 2015

In vivo characterization of the electrophysiological and astrocytic responses to a silicon neuroprobe implanted in the mouse neocortex

por Mols, Katrien, Musa, Silke, Nuttin, Bart, Lagae, Liesbet, Bonin, Vincent
Publicado 2017

A novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets

por Padmakumar, Manisha, Jaeken, Jaak, Ramaekers, Vincent, Lagae, Lieven, Greene, Daniel, Thys, Chantal, Van Geet, Chris, BioResource, NIHR, Stirrups, Kathleen, Downes, Kate, Turro, Ernest, Freson, Kathleen
Publicado 2019