Abstract | Referee: name/town | Subject/lecture |
---|---|---|
- | Beate Winner/Henry Wahlig | "TWS advanced scholarship: Introduction" |
Beate Winner, Erlangen | "Individualized human in vitro model for hereditary spastic paraplegia" | |
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 " |
Evan Reid, Cambridge/UK | "Roles of spastin in membrane traffic" | |
Elena Rugarli, Köln | "The m-AAA protease regulates mitochondrial fusion: implications for hereditary spastic paraplegia and spinocerebellar ataxia" | |
Christian Beetz, Jena | "Characterisation of a novel HSP mouse model" | |
Craig Blackstone, Betheshda/US | "Endoplasmic reticulum network defects as a pathogenic mechanism for the hereditary spastic paraplegias" | |
Daniela di Bella, Milano | "The mitochondrial m-AAA protease complex in the pathogenesis of hereditary spinocerebellar degenerations" | |
Ingo Kurth, Hamburg | "Mutations in FAM134B, encoding a novel Golgi protein, cause severe sensory and autonomic neuropathy" | |
A | Brunhilde Wirth, Köln | "Modifying genes in spinal muscular atrophy" |
Michael Sendtner, Würzburg | "Axonal mRNA Transport: Roles in motoneuron function and degeneration" | |
Lea Papić,Graz | "Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C" |
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