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Neurobiology of Aging|November 29, 2011
UNC13A is a modifier of survival in amyotrophic lateral sclerosisFrank P Diekstra, Paul W J van Vught, Wouter van Rheenen, et al.
International Journal of Molecular Sciences|October 23, 2021
Histone Deacetylase Inhibition Regulates Lipid Homeostasis in a Mouse Model of Amyotrophic Lateral SclerosisThibaut Burg, Elisabeth Rossaert, Matthieu Moisse, et al.
European Journal of Nuclear Medicine and Molecular Imaging|December 10, 2016
Positron emission tomography in amyotrophic lateral sclerosis: Towards targeting of molecular pathological hallmarksStefanie M A Willekens, Donatienne Van Weehaeghe, Philip Van Damme, et al.
Acta Neurologica Belgica|September 18, 2008
Normalization of 14-3-3 in CJDMaarten Schrooten, Wouter De Vooght, Sarah Weckhuysen, et al.
Bio-Protocol|March 4, 2021
Quantitative Nucleocytoplasmic Transport Assays in Cellular Models of NeurodegenerationJoni Vanneste, Thomas Vercruysse, Philip Van Damme, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 15, 2016
Patient-ventilator asynchrony, leaks and sleep in patients with amyotrophic lateral sclerosisBart Vrijsen, Dries Testelmans, Catharina Belge, et al.
Respirology (Carlton, Vic.)|April 5, 2017
Randomized cross-over trial of ventilator modes during non-invasive ventilation titration in amyotrophic lateral sclerosisBart Vrijsen, Bertien Buyse, Catharina Belge, et al.
JAMIA Open|January 29, 2024
Assessing the use of HL7 FHIR for implementing the FAIR guiding principles: a case study of the MIMIC-IV Emergency Department modulePhilip van Damme, Matthias Löbe, Nirupama Benis, et al.
Trends in Molecular Medicine|January 12, 2024
The sense of antisense therapies in ALSSien H Van Daele, Pegah Masrori, Philip Van Damme, et al.
Trends in Neurosciences|March 16, 2010
RNA metabolism and the pathogenesis of motor neuron diseasesRobin Lemmens, Melissa J Moore, Ammar Al-Chalabi, et al.
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