Research Highlights

Effects of SPG11 HSP studied

Posted - June 2013 in Research Highlights

Rapid disease progression found

Large study of AD-HSP in Portugal

Posted - in Research Highlights

New findings about SPG3 and SPG4

TFG gene causes neurodegeneration

Posted - in Research Highlights

Affects cell architecture

50+ genes explain less than 80% of HSP

Posted - in Research Highlights

Inheritance patterns can be misinterpreted.

Tiny worm sheds light

Posted - in Research Highlights

Seeking underlying cause of HSP

Rare SPG8 HSP described

Posted - in Research Highlights

Only 7 families identified worldwide

Stem cell research report

Posted - February 2013 in Research Highlights

What has been achieved and where to from here

Nasal stem cells help unlock HSP secrets

Posted - in Research Highlights

Promising progress towards a cure

Lines between diseases blur

Posted - in Research Highlights

Importance of mutation databases heightened

First HSP population study in Australia

Posted - in Research Highlights

Data supports findings elsewhere

SPG 3A and cognitive impairment

Posted - in Research Highlights

Decrease in glucose metabolism in the brain

Spastin’s role in axon regeneration

Posted - December 2012 in Research Highlights

No regrowth with mutated spastin

The Human Genome and how it works

Posted - in Research Highlights

Review of 30 papers by 500 scientists

SPG4 HSP study makes new findings

Posted - in Research Highlights

Wide ranging results

Fruit flies used to study Atlastin (SPG3A)

Posted - in Research Highlights

Role in healthy cell biology defined

Large study of SPG7 HSP

Posted - in Research Highlights

Many new findings emerge

Common factor in several forms of HSP

Posted - in Research Highlights

Bone morphogenic protein’s role in neurons

Stem Cell Research Project

Posted - September 2012 in Research Highlights

Progress Report September 2012

Mice with HSP used in study

Posted - in Research Highlights

Drugs reverse certain effects

SPG10 HSP and CMT type 2 strongly linked

Posted - in Research Highlights

Same gene mutation may cause both