1. A weakened interface in the P182L variant of HSP27 associated with severe Charcot‐Marie‐Tooth neuropathy causes aberrant binding to interacting proteins. (1st March 2021) Authors: Reid Alderson, T; Adriaenssens, Elias; Asselbergh, Bob; Pritišanac, Iva; Van Lent, Jonas; Gastall, Heidi Y; Wälti, Marielle A; Louis, John M; Timmerman, Vincent; Baldwin, Andrew J; LP Benesch, Justin Journal: EMBO journal Issue: Volume 40:Number 8(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Diffusion kurtosis imaging to detect amyloidosis in an APP/PS1 mouse model for Alzheimer's disease. Issue 4 (11th March 2013) Authors: Vanhoutte, Greetje; Pereson, Sandra; Delgado y Palacios, Rafael; Guns, Pieter‐Jan; Asselbergh, Bob; Veraart, Jelle; Sijbers, Jan; Verhoye, Marleen; Van, Christine; Van der, Annemie Journal: Magnetic resonance in medicine Issue: Volume 69:Issue 4(2013:Apr.) Page Start: 1115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies. Issue 6 (3rd June 2019) Authors: Haidar, Mansour; Asselbergh, Bob; Adriaenssens, Elias; De Winter, Vicky; Timmermans, Jean-Pierre; Auer-Grumbach, Michaela; Juneja, Manisha; Timmerman, Vincent Journal: Autophagy Issue: Volume 15:Issue 6(2019) Page Start: 1051 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Sensory neuropathy-causing mutations in ATL3 affect ER–mitochondria contact sites and impair axonal mitochondrial distribution. (18th October 2018) Authors: Krols, Michiel; Asselbergh, Bob; De Rycke, Riet; De Winter, Vicky; Seyer, Alexandre; Müller, Franz-Josef; Kurth, Ingo; Bultynck, Geert; Timmerman, Vincent; Janssens, Sophie Journal: Human molecular genetics Issue: Volume 28:Number 4(2019) Page Start: 615 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy. (7th February 2017) Authors: Atkinson, Derek; Nikodinovic Glumac, Jelena; Asselbergh, Bob; Ermanoska, Biljana; Blocquel, David; Steiner, Regula; Estrada-Cuzcano, Alejandro; Peeters, Kristien; Ooms, Tinne; De Vriendt, Els; Yang, Xiang-Lei; Hornemann, Thorsten; Milic Rasic, Vedrana; Jordanova, Albena Journal: Neurology Issue: Volume 88:Number 6(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy. (7th February 2017) Authors: Atkinson, Derek; Nikodinovic Glumac, Jelena; Asselbergh, Bob; Ermanoska, Biljana; Blocquel, David; Steiner, Regula; Estrada-Cuzcano, Alejandro; Peeters, Kristien; Ooms, Tinne; De Vriendt, Els; Yang, Xiang-Lei; Hornemann, Thorsten; Milic Rasic, Vedrana; Jordanova, Albena Journal: Neurology Issue: Volume 88:Number 6(2017) Page Start: 533 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗