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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