Abstract

Speaker 

Affiliation

Title

Session

        A

Albena Jordanova

Antwerp, Belgium

HSP in Bulgarian Gypsies – clinical and genetic studies

HSP: mutations and patient-derived cell models

Rebecca Schüle

Tübingen, Germany

Exome sequening in autosomal dominant HSP

         A

Beate Winner

Erlangen, Germany

Modeling HSP using induced pluripotent stem cells

Michaela Auer-Grumbach

Graz, Austria

A novel pathomechanism for a classical HSP gene underlies dHMN type V

other axonopathies I

Jan Kassubek

Ulm, Germany

News about the aetiology and pathogenesis of ALS 

Julian Grosskreutz

Jena, Germany

Biomarkers in Amyotrophic Lateral Sclerosis

         A

Brunhilde Wirth

Köln, Germany

Modifiers of spinal muscular atrophy

other axonopathies II

         A

Vincent Timmerman

Antwerp, Belgium

Understanding the pathomechanisms of Charcot-Marie-Tooth neuropathies

Craig Blackstone

Beteshda, U.S.A.

Common cellular pathogenic themes for the hereditary spastic paraplegias

pathomechanisms in major dominant forms of HSP

Evan Reid

Cambridge, UK

Stars and stripes- what spastin does at endosomes

Elena Rugarli

Köln, Germany

Expanding the spectrum of the cellular roles of spastin

         A

Günther Wöhlke

München, Germany

The dominant effect of mutant spastin subunits in wildtype background

        A

Jenny Hirst

Cambridge, UK

Identification of a fifth adaptor complex and its link with hereditary spastic paraplegia

further HSP proteins and models

Christoph Clemen

Köln, Germany

Characterization of Dictyostelium strains lacking strumpellin or  
expressing the HSP-causing N471D mutant strumpellin

Tobias Rasse

Tübingen, Germany

Spastic paraplegia mutation N256S in the neuronal microtubule motor KIF5A disrupts axonal transport in a Drosophila HSP model

        A

O' Sullivan

Cambridge UK

REEP and reticulon mutant phenotypes in Drosophila