Giovanni Stevanin

(Paris, FRA)

Genotype-phenotype correlations in SPG7

  PDF

William Newman

(Manchester, U.K.)

Rare disease gene identification in the frame of the 100.000 genomes project

  PDF

Stephan Zuchner

(Miami, U.S.A.)

Mutational burden analysis of interaction networks in inherited neuropathies

 PDF

Jong-Min Lee

(Boston, U.S.A.)

Identification of genetic factors that modify clinical onset of Huntington's disease

  PDF

Christine Klein

(Lübeck, GER)

Reduced penetrance in hereditary movement disorders

Thorsten Schmidt

(Tübingen, GER)

Targeting the intracellular localization of the affected protein as novel treatment approach in SCA3

William Griffiths

(Swansea, U.K.)

Cholesterol Metabolism in SPG5: Potential for Diagnosis and Therapy

Andrea Daga

(Conegliano, ITA)

Atlastin and reticulon interactions in the determination of ER morphology

Craig Blackstone

(Bethesda, U.S.A.)

New imaging tools for assessing ER morphology changes in HSP models

   PDF

Gautam Wali

(Sydney, AUS)

Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from HSP-patients

Tobias Walther

(Boston, U.S.A.)

Lipids, Organelles and Neurodegenerative disease