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Hereditary spastic paraplegias
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Neuropathy
OMIM - Spastic paraplegia
Comparative profiling in 13 muscle disease groups
OMIM - Brain CNS Motor Neuron and other Neuropathy Disorders
Facioscapulohumeral muscular dystrophy expression profiles in muscle
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Literature
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SPG3A-linked hereditary spastic paraplegia associated with cerebral glucose hypometabolism.
A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family.
Construction of wild-type and mutant SPAST vectors for the study of molecular mechanism of hereditar…
Novel SPG11 mutations in Chinese families with hereditary spastic paraplegia with thin corpus callos…
SPAST mutations in Australian patients with hereditary spastic paraplegia.
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Most Relevant Clinical Trials
Physiotherapy in Hereditary Spastic Paraplegia
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia
Identification of Modifying Factors in Hereditary Spastic Paraplegia
Effect of Dalfampridine in Patients With Hereditary Spastic Paraplegia
Improving Gait Adaptability in Hereditary Spastic Paraplegia
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