20th TWS symposium on November 26th in Essen

Live: on site and in the stream

The program of the 20th symposium:


Speaker Title
  TWS + Stephan Klebe Opening
PDF Kishore Raj Kumar (Syndney, AUS) Challenges and Controversies in the Genetic Diagnosis of HSP
PDF Fanny Mochel (Paris, FRA) Update on complex lipids in HSP
PDF Nathalie De Beukelaer (Leuven, BEL) Muscle Characteristics in Pediatric HSP vs. Bilateral Spastic Cerebral Palsy: An Exploartory Study
PDF Andrea Martinuzzi/Marinela Vavla (Lecco, ITA) Brain Magnetic Spectroscopy Imaging and HSP
PDF Rebecca Schüle (Tübingen, GER) PROSPAX
  Ludger Schöls (Tübingen, GER) 2021 TWS funding round: Introduction
PDF Catherine Rodger (Cambridge, GB) Development of AAV-mediated gene therapy for hereditary spastic paraplegia
PDF Darius Ebrahimi-Fakhari (Boston, USA) Characterization of ap4b1-/- zebrafish as a novel in vivo model of SPG47 and its application in small molecule screens
  Gerald Fischer (AUT) Adolf-Strumpell-Prize for HSP-Therapy: Introduction
PDF Francesca Sardina (Rom, ITA) Spastin recovery in hereditary spastic paraplegia by preventing neddylation-dependent degradation
PDF Peter Baas (Philadelphia, USA) Mechanistic Route to Therapy for SPG4 Hereditary Spastic Paraplegia
PDF Aurora Pujol (Barcelona, ESP) Novel metabolic genes causing HSP: the SHMT2 and PIA4KA cases
PDF Stefan Hauser (Tübingen, GER) Comparative transcrisptional profiling of motor neuron disorder-associated genes in various human cell culture models
PDF Ziv Gan-Or (Montreal, CAN) CanHSP: genetic and clinical lessons on HSP from a Canadian consortium
PDF Darius Ebrahimi-Fakhari (Boston, USA) AP-4-associated Hereditary Spastic Paraplegia – A Translational Approach to An Ultra-rare Disease
PDF Craig Blackstone (Boston, USA) New Insights into ER Morphology Dysregulation in Hereditary Spastic Paraplegias
    Concluding remarks