5 studies found for:    "L1 syndrome" OR "Spastic Paraplegia, Hereditary" OR "Hereditary Spastic Paraplegia"
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"L1 syndrome" OR "Spastic Paraplegia, Hereditary" OR "Hereditary Spastic Paraplegia" (5 records)
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Rank Status Study
1 Completed Nuclear Magnetic Spectroscopy Imaging to Evaluate Primary Lateral Sclerosis, Hereditary Spastic Paraplegia and Amyotrophic Lateral Sclerosis
Conditions: Primary Lateral Sclerosis;   Hereditary Spastic Paraplegia;   Amyotrophic Lateral Sclerosis
Intervention:
2 Recruiting Genetic and Physical Study of Childhood Nerve and Muscle Disorders
Conditions: Muscular Dystrophies;   Muscle Myopathies;   Hereditary Spastic Paraplegias;   Inherited Neuropathies;   Inherited Neuromuscular Conditions
Intervention:
3 Recruiting Phenotype, Genotype & Biomarkers in ALS and Related Disorders
Conditions: Amyotrophic Lateral Sclerosis;   Frontotemporal Dementia;   Primary Lateral Sclerosis;   Hereditary Spastic Paraplegia;   Progressive Muscular Atrophy;   Multisystem Proteinopathy
Intervention:
4 Active, not recruiting Therapeutic Metabolic Intervention in Patients With Spastic Paraplegia SPG5
Condition: Spastic Paraplegia, Hereditary
Interventions: Drug: Xenbilox;   Dietary Supplement: Resveratrol;   Drug: Tahor
5 Active, not recruiting Validation of Biomarkers in Amyotrophic Lateral Sclerosis (ALS)
Conditions: Amyotrophic Lateral Sclerosis;   Lou Gehrig's Disease;   Primary Lateral Sclerosis;   Nervous System Diseases;   Hereditary Spastic Paraparesis
Intervention: Other: No intervention

Indicates status has not been verified in more than two years