9 studies found for: "L1 syndrome" OR "Spastic Paraplegia, Hereditary" OR "Hereditary Spastic Paraplegia"
|1||Active, not recruiting||
Effects of Botulinum Toxin Injections in Patients With Hereditary Spastic Paraplegia
Disease Natural History and Biomarkers of SPG3A, SPG4A, and SPG31
Nuclear Magnetic Spectroscopy Imaging to Evaluate Primary Lateral Sclerosis, Hereditary Spastic Paraplegia and Amyotrophic Lateral Sclerosis
Studying Cognition in SPG4
|5||Active, not recruiting||
Therapeutic Metabolic Intervention in Patients With Spastic Paraplegia SPG5
|6||Enrolling by invitation||
A Patient Centric Motor Neuron Disease Activities of Daily Living Scale
Genetic and Physical Study of Childhood Nerve and Muscle Disorders
Phenotype, Genotype & Biomarkers in ALS and Related Disorders
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
† Study has passed its completion date and status has not been verified in more than two years.