by Claeys, Kristl G
Published in Developmental medicine and child neurology (01.03.2020)

by Stevens, Olivier, Claeys, Kristl G, Poesen, Koen, Saegeman, Veroniek, Van Damme, Philip
Published in JAMA neurology (01.01.2017)

by Gille, Benjamin, De Schaepdryver, Maxim, Dedeene, Lieselot, Goossens, Janne, Claeys, Kristl G, Van Den Bosch, Ludo, Tournoy, Jos, Van Damme, Philip, Poesen, Koen
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2019)

by Stenzel, Werner, Preuße, Corinna, Allenbach, Yves, Pehl, Debora, Junckerstorff, Reimar, Heppner, Frank L, Nolte, Kay, Aronica, Eleonora, Kana, Veronika, Rushing, Elisabeth, Schneider, Udo, Claeys, Kristl G, Benveniste, Olivier, Weis, Joachim, Goebel, Hans H
Published in Neurology (31.03.2015)

by Huysmans, Lotte, De Wel, Bram, Claeys, Kristl G, Maes, Frederik
Published in Frontiers in neurology (24.05.2023)

by Weis, Joachim, Claeys, Kristl G., Roos, Andreas, Azzedine, Hamid, Katona, Istvan, Schröder, J. Michael, Senderek, Jan
Published in Acta Neuropathologica (01.04.2017)

by De Wel, Bram, De Schaepdryver, Maxim, Poesen, Koen, Claeys, Kristl G.
Published in Annals of clinical and translational neurology (01.08.2022)

by Claeys, Kristl G, Kushlaf, Hani, Raza, Syed, Hummel, Noemi, Shohet, Simon, Keyzor, Ian, Kopiec, Agnieszka, Graham, Ryan, Fox, Brian, Schoser, Benedikt
Published in Orphanet journal of rare diseases (11.04.2024)

by Altmann, Judith, Büchner, Boriana, Nadaj-Pakleza, Aleksandra, Schäfer, Jochen, Jackson, Sandra, Lehmann, Diana, Deschauer, Marcus, Kopajtich, Robert, Lautenschläger, Ronald, Kuhn, Klaus A., Karle, Kathrin, Schöls, Ludger, Schulz, Jörg B., Weis, Joachim, Prokisch, Holger, Kornblum, Cornelia, Claeys, Kristl G., Klopstock, Thomas
Published in Journal of neurology (01.05.2016)

by Stenton, Sarah L., Piekutowska‐Abramczuk, Dorota, Kulterer, Lea, Kopajtich, Robert, Claeys, Kristl G., Ciara, Elżbieta, Eisen, Johannes, Płoski, Rafał, Pronicka, Ewa, Malczyk, Katarzyna, Wagner, Matias, Wortmann, Saskia B., Prokisch, Holger
Published in Human mutation (01.03.2021)

by Schnitzler, Lukas J, Schreckenbach, Tobias, Nadaj-Pakleza, Aleksandra, Stenzel, Werner, Rushing, Elisabeth J, Van Damme, Philip, Ferbert, Andreas, Petri, Susanne, Hartmann, Christian, Bornemann, Antje, Meisel, Andreas, Petersen, Jens A, Tousseyn, Thomas, Thal, Dietmar R, Reimann, Jens, De Jonghe, Peter, Martin, Jean-Jacques, Van den Bergh, Peter Y, Schulz, Jörg B, Weis, Joachim, Claeys, Kristl G
Published in Orphanet journal of rare diseases (11.05.2017)

by De Wel, Bram, Huysmans, Lotte, Peeters, Ronald, Ghysels, Stefan, Byloos, Kris, Putzeys, Guido, Maes, Frederik, Dupont, Patrick, Claeys, Kristl G.
Published in Journal of cachexia, sarcopenia and muscle (01.10.2024)

by Berrih-Aknin, Sonia, Palace, Jacqueline, Meisel, Andreas, Claeys, Kristl G, Muppidi, Srikanth, Saccà, Francesco, Amini, Fatemeh, Larkin, Mark, Quinn, Casey, Beauchamp, Jon, Philips, Glenn, De Ruyck, Femke, Ramirez, Joyce, Paci, Sandra
Published in BMJ open (11.05.2023)

by Cordts, Isabell, Bodart, Nicolas, Hartmann, Kathi, Karagiorgou, Katerina, Tzartos, John S., Mei, Lin, Reimann, Jens, Van Damme, Philip, Rivner, Michael H., Vigneron, Alain, Weis, Joachim, Schulz, Jörg B., Tzartos, Socrates J., Claeys, Kristl G.
Published in Journal of neurology (01.06.2017)

by Palmio, Johanna, Leonard-Louis, Sarah, Sacconi, Sabrina, Savarese, Marco, Penttilä, Sini, Semmler, Anna-Lena, Kress, Wolfram, Mozaffar, Tahseen, Lai, Tim, Stojkovic, Tanya, Berardo, Andres, Reisin, Ricardo, Attarian, Shahram, Urtizberea, Andoni, Cobo, Ana Maria, Maggi, Lorenzo, Kurbatov, Sergei, Nikitin, Sergei, Milisenda, José C., Fatehi, Farzad, Raimondi, Monika, Silveira, Fernando, Hackman, Peter, Claeys, Kristl G., Udd, Bjarne
Published in Journal of neurology (01.03.2019)

by De Wel, Bram, Huysmans, Lotte, Depuydt, Christophe E., Goosens, Veerle, Peeters, Ronald, Santos, Filipa P., Thal, Dietmar R., Dupont, Patrick, Maes, Frederik, Claeys, Kristl G.
Published in Journal of cachexia, sarcopenia and muscle (01.06.2023)

by Bevilacqua, Jorge A, Guecaimburu Ehuletche, Maria Del Rosario, Perna, Abayuba, Dubrovsky, Alberto, Franca, Jr, Marcondes C, Vargas, Steven, Hegde, Madhuri, Claeys, Kristl G, Straub, Volker, Daba, Nadia, Faria, Roberta, Periquet, Magali, Sparks, Susan, Thibault, Nathan, Araujo, Roberto
Published in Orphanet journal of rare diseases (13.01.2020)

by Østergaard, Sofie Thurø, Johnson, Katherine, Stojkovic, Tanya, Krag, Thomas, De Ridder, Willem, De Jonghe, Peter, Baets, Jonathan, Claeys, Kristl G, Fernández-Torrón, Roberto, Phillips, Lauren, Topf, Ana, Colomer, Jaume, Nafissi, Shahriar, Jamal-Omidi, Shirin, Bouchet-Seraphin, Celine, Leturcq, France, MacArthur, Daniel G, Lek, Monkol, Xu, Liwen, Nelson, Isabelle, Straub, Volker, Vissing, John
Published in Journal of neurology, neurosurgery and psychiatry (01.05.2018)

by Dewilde, Sarah, Philips, Glenn, Paci, Sandra, Beauchamp, Jon, Chiroli, Silvia, Quinn, Casey, Day, Laura, Larkin, Mark, Palace, Jacqueline, Berrih-Aknin, Sonia, Claeys, Kristl G, Muppidi, Srikanth, Mantegazza, Renato, Saccà, Francesco, Meisel, Andreas, Bassez, Guillaume, Murai, Hiroyuki, Janssen, MF
Published in BMJ open (31.01.2023)

by Bozkurt, Ahmet, Claeys, Kristl G, Schrading, Simone, Rödler, Jana V, Altinova, Haktan, Schulz, Jörg B, Weis, Joachim, Pallua, Norbert, van Neerven, Sabien G A
Published in European journal of medical research (22.09.2017)