Inflammatory markers in cerebrospinal fluid: independent prognostic biomarkers in amyotrophic lateral sclerosis?
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)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2019)
Get full text
Journal Article
Women with symptoms of a urinary tract infection but a negative urine culture: PCR-based quantification of Escherichia coli suggests infection in most cases
Heytens, S., De Sutter, A., Coorevits, L., Cools, P., Boelens, J., Van Simaey, L., Christiaens, T., Vaneechoutte, M., Claeys, G.
Published in Clinical microbiology and infection (01.09.2017)
Published in Clinical microbiology and infection (01.09.2017)
Get full text
Journal Article
Therapeutic drug monitoring-based dose optimisation of piperacillin and meropenem: a randomised controlled trial
De Waele, Jan J., Carrette, S., Carlier, M., Stove, V., Boelens, J., Claeys, G., Leroux-Roels, I., Hoste, E., Depuydt, P., Decruyenaere, J., Verstraete, A. G.
Published in Intensive care medicine (01.03.2014)
Published in Intensive care medicine (01.03.2014)
Get full text
Journal Article
Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy
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)
Published in Neurology (31.03.2015)
Get more information
Journal Article
Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures
Vanherpe, P, Fieuws, S, D'Hondt, A, Bleyenheuft, C, Demaerel, P, De Bleecker, J, Van den Bergh, P, Baets, J, Remiche, G, Verhoeven, K, Delstanche, S, Toussaint, M, Buyse, B, Van Damme, P, Depuydt, C E, Claeys, K G
Published in Orphanet journal of rare diseases (05.04.2020)
Published in Orphanet journal of rare diseases (05.04.2020)
Get full text
Journal Article
Minimal clinically important differences in six-minute walking distance in late-onset Pompe disease
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)
Published in Orphanet journal of rare diseases (11.04.2024)
Get full text
Journal Article
Towards a functional pathology of hereditary neuropathies
Weis, Joachim, Claeys, Kristl G., Roos, Andreas, Azzedine, Hamid, Katona, Istvan, Schröder, J. Michael, Senderek, Jan
Published in Acta Neuropathologica (01.04.2017)
Published in Acta Neuropathologica (01.04.2017)
Get full text
Journal Article
Book Review
Uropathogen distribution and antimicrobial susceptibility in uncomplicated cystitis in Belgium, a high antibiotics prescribing country: 20-year surveillance
Heytens, S., Boelens, J., Claeys, G., DeSutter, A., Christiaens, T.
Published in European journal of clinical microbiology & infectious diseases (2017)
Published in European journal of clinical microbiology & infectious diseases (2017)
Get full text
Journal Article
Expanded phenotypic spectrum of the m.8344A>G “MERRF” mutation: data from the German mitoNET registry
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)
Published in Journal of neurology (01.05.2016)
Get full text
Journal Article
Expanding the clinical and genetic spectrum of FDXR deficiency by functional validation of variants of uncertain significance
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)
Published in Human mutation (01.03.2021)
Get full text
Journal Article
Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases
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)
Published in Orphanet journal of rare diseases (11.05.2017)
Get full text
Journal Article
Patient-reported impact of myasthenia gravis in the real world: findings from a digital observational survey-based study (MyRealWorld MG)
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)
Published in BMJ open (11.05.2023)
Get full text
Journal Article
Histopathological correlations and fat replacement imaging patterns in recessive limb‐girdle muscular dystrophy type 12
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)
Published in Journal of cachexia, sarcopenia and muscle (01.06.2023)
Get full text
Journal Article
The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease
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)
Published in Orphanet journal of rare diseases (13.01.2020)
Get full text
Journal Article