Research Highlights
SPG48 HSP studied in depth
Posted - December 2016 in Research Highlights
Multiple associated complications
Australian success with whole genome sequencing
Posted - September 2016 in Research Highlights
Higher detection rates for HSP mutations
Recessive SPG35 HSP inherited from just one parent
Posted - in Research Highlights
Major implications for genetic counselling
Large Czech study of SPAST HSP
Posted - in Research Highlights
327 HSPers from 263 families gene tested
New HSP genetic findings
Posted - in Research Highlights
From Iran, Germany, China, Greece, Japan, Pakistan and Hungary
SPAST (SPG4) HSP mechanism explained
Posted - June 2016 in Research Highlights
Potential drug treatment identified
Potential therapeutic avenues for HSP
Posted - in Research Highlights
Biomarkers investigated in animal models
Exome sequencing helps with HSP diagnosis
Posted - in Research Highlights
New gene-disease associations found
The science of patient input
Posted - in Research Highlights
Integrating patient needs and priorities
New Findings on SPG11 HSP mechanism
Posted - in Research Highlights
Potential treatment target identified
Late-onset spastic paraplegia type 10 (SPG10)
Posted - May 2016 in Research Highlights
First-time discovered in an Asian family
REEP1 (SPG31) found with recessive inheritance
Posted - in Research Highlights
Previously associated only with dominant form
New HSP genetic findings
Posted - in Research Highlights
From Japan, Poland, England, China, Hungary, Morocco, Canada, Italy and the USA
Developing a ‘natural history’ of HSP
Posted - February 2016 in Research Highlights
Large German study lays the foundation
Atlastin (SPG 3A) investigated
Posted - in Research Highlights
Questions raised about regulation and role
SPG 8 HSP loss-of-function theory questioned
Posted - in Research Highlights
Implications for alternative gain-of-function hypothesis
