Vascular changes and perifascicular muscle fiber damage in dermatomyositis: another question of the chicken or the egg that is on our mind

Por De Paepe, Boel
Publicado no Ann Transl Med (2017)

Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras

Por De Paepe, Boel
Publicado no Biomolecules (2019)

Progressive Skeletal Muscle Atrophy in Muscular Dystrophies: A Role for Toll-Like Receptor-Signaling in Disease Pathogenesis

Por De Paepe, Boel
Publicado no Int J Mol Sci (2020)

Scanning for Therapeutic Targets within the Cytokine Network of Idiopathic Inflammatory Myopathies

Por De Paepe, Boel, Zschüntzsch, Jana
Publicado no Int J Mol Sci (2015)

A Critical Assessment of the Therapeutic Potential of Resveratrol Supplements for Treating Mitochondrial Disorders

Por De Paepe, Boel, Van Coster, Rudy
Publicado no Nutrients (2017)

Cytokines and Chemokines as Regulators of Skeletal Muscle Inflammation: Presenting the Case of Duchenne Muscular Dystrophy

Por De Paepe, Boel, De Bleecker, Jan L.
Publicado em 2013

The Tumor Necrosis Factor Superfamily of Cytokines in the Inflammatory Myopathies: Potential Targets for Therapy

Por De Paepe, Boel, Creus, Kim K., De Bleecker, Jan L.
Publicado em 2012

Anti-Inflammatory and General Glucocorticoid Physiology in Skeletal Muscles Affected by Duchenne Muscular Dystrophy: Exploration of Steroid-Sparing Agents

Por Herbelet, Sandrine, Rodenbach, Arthur, De Paepe, Boel, De Bleecker, Jan L.
Publicado no Int J Mol Sci (2020)

Heat-Shock Proteins in Autoimmunity

Por Moudgil, Kamal D., Thompson, Stephen J., Geraci, Fabiana, De Paepe, Boel, Shoenfeld, Yehuda
Publicado em 2013

Myo-Inositol Transporter SLC5A3 Associates with Degenerative Changes and Inflammation in Sporadic Inclusion Body Myositis

Por De Paepe, Boel, Merckx, Caroline, Jarošová, Jana, Cannizzaro, Miryam, De Bleecker, Jan L.
Publicado no Biomolecules (2020)

Induction of Osmolyte Pathways in Skeletal Muscle Inflammation: Novel Biomarkers for Myositis

Por De Paepe, Boel, Zschüntzsch, Jana, Šokčević, Tea, Weis, Joachim, Schmidt, Jens, De Bleecker, Jan L.
Publicado no Front Neurol (2018)

Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster

Por Verhelst, Helene, Verloo, Patrick, Dhondt, Karlien, De Paepe, Boel, Menten, Björn, Dalmau, Josep, Van Coster, Rudy
Publicado em 2010

Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

Por Seneca, Sara, Vancampenhout, Kim, Van Coster, Rudy, Smet, Joél, Lissens, Willy, Vanlander, Arnaud, De Paepe, Boel, Jonckheere, An, Stouffs, Katrien, De Meirleir, Linda
Publicado no Eur J Hum Genet (2015)

A Bumpy Ride on the Diagnostic Bench of Massive Parallel Sequencing, the Case of the Mitochondrial Genome

Por Vancampenhout, Kim, Caljon, Ben, Spits, Claudia, Stouffs, Katrien, Jonckheere, An, De Meirleir, Linda, Lissens, Willy, Vanlander, Arnaud, Smet, Joél, De Paepe, Boel, Van Coster, Rudy, Seneca, Sara
Publicado no PLoS One (2014)

Clinical variability in neurohepatic syndrome due to combined mitochondrial DNA depletion and Gaucher disease

Por Harvengt, Julie, Wanty, Catherine, De Paepe, Boel, Sempoux, Christine, Revencu, Nicole, Smet, Joél, Van Coster, Rudy, Lissens, Willy, Seneca, Sara, Weekers, Laurent, Sokal, Etienne, Debray, François-Guillaume
Publicado no Mol Genet Metab Rep (2014)

Nanoscopic X-ray fluorescence imaging and quantification of intracellular key-elements in cryofrozen Friedreich’s ataxia fibroblasts

Por De Samber, Björn, Meul, Eline, Laforce, Brecht, De Paepe, Boel, Smet, Joél, De Bruyne, Michiel, De Rycke, Riet, Bohic, Sylvain, Cloetens, Peter, Van Coster, Rudy, Vandenabeele, Peter, Vanden Berghe, Tom
Publicado no PLoS One (2018)

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects

Por Roels, Frank, Verloo, Patrick, Eyskens, François, François, Baudouin, Seneca, Sara, De Paepe, Boel, Martin, Jean-Jacques, Meersschaut, Valerie, Praet, Marleen, Scalais, Emmanuel, Espeel, Marc, Smet, Joél, Van Goethem, Gert, Van Coster, Rudy
Publicado em 2009

Localization and Expression of Nuclear Factor of Activated T-Cells 5 in Myoblasts Exposed to Pro-inflammatory Cytokines or Hyperosmolar Stress and in Biopsies from Myositis Patient...

Por Herbelet, Sandrine, De Vlieghere, Elly, Gonçalves, Amanda, De Paepe, Boel, Schmidt, Karsten, Nys, Eline, Weynants, Laurens, Weis, Joachim, Van Peer, Gert, Vandesompele, Jo, Schmidt, Jens, De Wever, Olivier, De Bleecker, Jan L.
Publicado no Front Physiol (2018)

New insights into the phenotype of FARS2 deficiency

Por Vantroys, Elise, Larson, Austin, Friederich, Marisa, Knight, Kaz, Swanson, Michael A., Powell, Christopher A., Smet, Joél, Vergult, Sarah, De Paepe, Boel, Seneca, Sara, Roeyers, Herbert, Menten, Björn, Minczuk, Michal, Vanlander, Arnaud, Van Hove, Johan, Van Coster, Rudy
Publicado no Mol Genet Metab (2017)

Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES

Por De Ridder, Willem, Nelson, Isabelle, Asselbergh, Bob, De Paepe, Boel, Beuvin, Maud, Ben Yaou, Rabah, Masson, Cécile, Boland, Anne, Deleuze, Jean-François, Maisonobe, Thierry, Eymard, Bruno, Symoens, Sofie, Schindler, Roland, Brand, Thomas, Johnson, Katherine, Töpf, Ana, Straub, Volker, De Jonghe, Peter, De Bleecker, Jan L., Bonne, Gisèle, Baets, Jonathan
Publicado no Neurol Genet (2019)