By A Mystery Man Writer
Physiotherapy proves helpful
Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis. - Abstract - Europe PMC
Innovative mobility device - HSP Research Foundation
Loss of spatacsin function alters lysosomal lipid clearance leading to upper and lower motor neuron degeneration - ScienceDirect
Therapeutic strategies for SPG4 - HSP Research Foundation
Hereditary spastic paraplegia type 56: what a mouse can tell - a narrative review
Loss of spatacsin function alters lysosomal lipid clearance leading to upper and lower motor neuron degeneration - ScienceDirect
Innovative mobility device - HSP Research Foundation
PDF) The Intra- and Inter-Rater Reliability of an Instrumented Spasticity Assessment in Children with Cerebral Palsy
Better understanding spasticity - HSP Research Foundation
Experienced complaints, activity limitations and loss of motor capacities in patients with pure hereditary spastic paraplegia: a web-based survey in the Netherlands, Orphanet Journal of Rare Diseases
PDF) A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene
Spastic Paraplegia Foundation - Hereditary Spastic Paraplegia & Primary Lateral SclerosisF
PDF) Functional efects of botulinum toxin type-A treatment and subsequent stretching of spastic calf muscles: A study in patients with hereditary spastic paraplegia
Spinal Cord Injuries: Non-traumatic, Nursing CEU, AOTA