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Publications by P. Hedera
Hereditary Spastic Paraplegia-Associated Mutations in the NIPA1 Gene and Its Caenorhabditis Elegans Homolog Trigger Neural Degeneration in Vitro and in Vivo Through a Gain-Of-Function Mechanism
Journal of Neuroscience
Neuroscience
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Hereditary Spastic Paraplegia Caused by Mutations in the SPG4 Gene
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Autosomal Dominant Hereditary Spastic Paraplegia: Novel Mutations in the REEP1 Gene (SPG31)
BMC Medical Genetics
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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia
American Journal of Human Genetics
Genetics
Three Novel Mutations of the Spastin Gene in Chinese Patients With Hereditary Spastic Paraplegia
Archives of Neurology
Hereditary Ataxia and Spastic Paraplegia in Portugal
JAMA Neurology
Neurology
Structural Consequences of Hereditary Spastic Paraplegia Disease-Related Mutations in Kinesin
Proceedings of the National Academy of Sciences of the United States of America
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Truncating Mutations inSPASTpatients Are Associated With a High Rate of Psychiatric Comorbidities in Hereditary Spastic Paraplegia
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Hereditary Spastic Paraplegia
Schweizer Archiv für Neurologie und Psychiatrie
The Hsp60-(p.V98I) Mutation Associated With Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Bothin Vitroandin Vivo
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology