Beate Winner/Henry Wahlig

"TWS advanced scholarship: Introduction"

A

Beate Winner, Erlangen

"Individualized human in vitro model for hereditary spastic paraplegia"

A

Christian Hübner, Jena

"Establishing neuron like cells from skin derived precursor cells in SPG4 patients"

Rebecca Schüle, Tübingen

"What is going wrong in SPG10? Genetics - pathomechanism - animal models "

A

Evan Reid, Cambridge/UK

"Roles of spastin in membrane traffic"

A

Elena Rugarli, Köln

"The m-AAA protease regulates mitochondrial fusion: implications for hereditary spastic paraplegia and spinocerebellar ataxia"

A

Christian Beetz, Jena

"Characterisation of a novel HSP mouse model"

A

Craig Blackstone, Betheshda/US

"Endoplasmic reticulum network defects as a pathogenic mechanism for the hereditary spastic paraplegias"

A

Daniela di Bella, Milano

"The mitochondrial m-AAA protease complex in the pathogenesis of hereditary spinocerebellar degenerations"

A

Ingo Kurth, Hamburg

"Mutations in FAM134B, encoding a novel Golgi protein, cause severe sensory and autonomic neuropathy"

Brunhilde Wirth, Köln

"Modifying genes in spinal muscular atrophy"

A

Michael Sendtner, Würzburg

"Axonal mRNA Transport: Roles in motoneuron function and degeneration"

A

Lea Papić,Graz

"Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C"