Automated MRI quantification of volumetric per-muscle fat fractions in the proximal leg of patients with muscular dystrophies

por Huysmans, Lotte, De Wel, Bram, Claeys, Kristl G., Maes, Frederik
Publicado 2023

Biochemical and clinical biomarkers in adult SMA 3–4 patients treated with nusinersen for 22 months

por De Wel, Bram, De Schaepdryver, Maxim, Poesen, Koen, Claeys, Kristl G.
Publicado 2022

Six-Minute Walk Distance Is a Useful Outcome Measure to Detect Motor Decline in Treated Late-Onset Pompe Disease Patients

por Claeys, Kristl G., D’Hondt, Ann, Fache, Lucas, Peers, Koen, Depuydt, Christophe E.
Publicado 2022

Anterior interosseous mononeuropathy associated with HEV infection

por Swinnen, Bart, Boeynaems, Steven, Schrooten, Maarten, Saegeman, Veroniek, Claeys, Kristl G., Van Damme, Philip
Publicado 2017

Prognostic value of neurofilament light chain in chronic inflammatory demyelinating polyneuropathy

por Godelaine, Joris, De Schaepdryver, Maxim, Bossuyt, Xavier, Van Damme, Philip, Claeys, Kristl G, Poesen, Koen
Publicado 2021

A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium

por De Bleecker, Jan L., Claeys, Kristl G., Delstanche, Stéphanie, Van Parys, Vinciane, Baets, Jonathan, Tilleux, Sébastien, Remiche, Gauthier
Publicado 2023

A Patient with Neonatal Cholestasis

por Claeys, Kristl G., Breysem, Luc, Legius, Eric, Brems, Hilde, Cassiman, David, Moisse, Matthieu, Vermeersch, Pieter, Levtchenko, Elena, Jaeken, Jaak
Publicado 2021

Metabolic Syndrome, Neurotoxic 1-Deoxysphingolipids and Nervous Tissue Inflammation in Chronic Idiopathic Axonal Polyneuropathy (CIAP)

por Hube, Larissa, Dohrn, Maike F., Karsai, Gergely, Hirshman, Sarah, Van Damme, Philip, Schulz, Jörg B., Weis, Joachim, Hornemann, Thorsten, Claeys, Kristl G.
Publicado 2017

Peptides From the Variable Domain of Immunoglobulin G as Biomarkers in Chronic Inflammatory Demyelinating Polyradiculoneuropathy

por Godelaine, Joris, Chitale, Yamini, De Moor, Bart, Mathieu, Chantal, Ancheva, Lina, Van Damme, Philip, Claeys, Kristl G., Bossuyt, Xavier, Carpentier, Sebastien, Poesen, Koen
Publicado 2023

Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix

por Bozkurt, Ahmet, Claeys, Kristl G., Schrading, Simone, Rödler, Jana V., Altinova, Haktan, Schulz, Jörg B., Weis, Joachim, Pallua, Norbert, van Neerven, Sabien G. A.
Publicado 2017

Unraveling the Molecular Basis of the Dystrophic Process in Limb-Girdle Muscular Dystrophy LGMD-R12 by Differential Gene Expression Profiles in Diseased and Healthy Muscles

por Depuydt, Christophe E., Goosens, Veerle, Janky, Rekin’s, D’Hondt, Ann, De Bleecker, Jan L., Noppe, Nathalie, Derveaux, Stefaan, Thal, Dietmar R., Claeys, Kristl G.
Publicado 2022

RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvement

por Van Daele, Sien H., Moisse, Matthieu, Race, Valérie, Van Eesbeeck, Amélie, Keldermans, Liesbeth, Vermeer, Sascha, Van Esch, Hilde, Claeys, Kristl G., Van Damme, Philip
Publicado 2021

Histopathological correlations and fat replacement imaging patterns in recessive limb‐girdle muscular dystrophy type 12

por 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.
Publicado 2023

Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?

por Werheid, Friederike, Azzedine, Hamid, Zwerenz, Eva, Bozkurt, Ahmet, Moeller, Marcus J., Lin, Lilian, Mull, Michael, Häusler, Martin, Schulz, Jörg B., Weis, Joachim, Claeys, Kristl G.
Publicado 2016

The Proximal Medial Sural Nerve Biopsy Model: A Standardised and Reproducible Baseline Clinical Model for the Translational Evaluation of Bioengineered Nerve Guides

por Bozkurt, Ahmet, van Neerven, Sabien G. A., Claeys, Kristl G., O'Dey, Dan mon, Sudhoff, Angela, Brook, Gary A., Sellhaus, Bernd, Schulz, Jörg B., Weis, Joachim, Pallua, Norbert
Publicado 2014

Serum neurofilament heavy chains as early marker of motor neuron degeneration

por De Schaepdryver, Maxim, Goossens, Janne, De Meyer, Steffi, Jeromin, Andreas, Masrori, Pegah, Brix, Britta, Claeys, Kristl G., Schaeverbeke, Jolien, Adamczuk, Katarzyna, Vandenberghe, Rik, Van Damme, Philip, Poesen, Koen
Publicado 2019

Patient-reported impact of myasthenia gravis in the real world: findings from a digital observational survey-based study (MyRealWorld MG)

por 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
Publicado 2023

Patient-reported impact of myasthenia gravis in the real world: protocol for a digital observational study (MyRealWorld MG)

por Berrih-Aknin, Sonia, Claeys, Kristl G, Law, Nancy, Mantegazza, Renato, Murai, Hiroyuki, Saccà, Francesco, Dewilde, Sarah, Janssen, Mathieu F, Bagshaw, Emma, Kousoulakou, Hara, Larkin, Mark, Beauchamp, Jon, Leighton, Trevor, Paci, Sandra
Publicado 2021

Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibers

por Dohrn, Maike F., Heller, Corina, Zengeler, Diana, Obermaier, Carolin D., Biskup, Saskia, Weis, Joachim, Nikolin, Stefan, Claeys, Kristl G., Schöne, Ulrike, Beijer, Danique, Winter, Natalie, Achenbach, Pascal, Gess, Burkhard, Schulz, Jörg B., Mulahasanovic, Lejla
Publicado 2022

The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease

por Bevilacqua, Jorge A., Guecaimburu Ehuletche, Maria del Rosario, Perna, Abayuba, Dubrovsky, Alberto, Franca, Marcondes C., Vargas, Steven, Hegde, Madhuri, Claeys, Kristl G., Straub, Volker, Daba, Nadia, Faria, Roberta, Periquet, Magali, Sparks, Susan, Thibault, Nathan, Araujo, Roberto
Publicado 2020