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Research Highlights

KIF5 study relevant to SPG10 HSP

Neuronal transport mechanism identified

Dementia in some SPG4 HSPers

Linked with Alzheimer’s gene

Rare HSP linked to Huntington’s disease

Both detected in one family over generations

Epilepsy and HSP

SPG6 risk identified

Link between HSP & Charcot-Marie-Tooth disease

SPG10 and CMT2 may be from same gene mutation

SPG18 complicated HSP described

List of affected cellular functions expanding

SPG4 mutations studied

Process for regulating Spastin levels defined

Stem cell research progress report, May 2011

Research project on target

Gender analysis of SPG4 HSP

Significantly more males than females

Atlastin function in cells explored

Important for cell membrane fusion

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Newer posts Page 1 … Page 35 … Page 45 Older posts

HSP Research Foundation

Welcome to the HSP Research Foundation - created in 2005 to find a cure for Hereditary Spastic Paraplegia - an inherited, degenerative disease affecting mainly the legs, causing muscle weakness, spasticity and severely impairing walking. Read more »

Information on this website and resources to which we have links are general knowledge about HSP. We are not medical professionals, nor do we offer medical advice. Always consult your own medical professionals regarding your particular circumstances.

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