Dementia in SPG4 hereditary spastic paraplegia: Clinical, genetic, and neuropathologic evidence
Murphy et al.
Neurology 2009;73:378-384.
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CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5
Goizet et al.
Brain 2009;132:1589-1600.
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Differentiation of Hereditary Spastic Paraparesis From Primary Lateral Sclerosis in Sporadic Adult-Onset Upper Motor Neuron Syndromes
Brugman et al.
Arch Neurol 2009;66:509-514.
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Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes
Brugman et al.
Neurology 2008;71:1500-1505.
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Functional characterization of NIPA2, a selective Mg2+ transporter
Goytain et al.
Am. J. Physiol. Cell Physiol. 2008;295:C944-C953.
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A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation
Warnecke et al.
Neurology 2007;69:368-375.
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NIPA1(SPG6), the Basis for Autosomal Dominant Form of Hereditary Spastic Paraplegia, Encodes a Functional Mg2+ Transporter
Goytain et al.
J. Biol. Chem. 2007;282:8060-8068.
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Childhood-Onset Spastic Paraplegia With NIPA1 Gene Mutation
Bien-Willner et al.
J Child Neurol 2006;21:974-977.
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The Spastic Paraplegia Rating Scale (SPRS): A reliable and valid measure of disease severity
Schule et al.
Neurology 2006;67:430-434.
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Eight Novel Mutations in SPG4 in a Large Sample of Patients With Hereditary Spastic Paraplegia.
Crippa et al.
Arch Neurol 2006;63:750-755.
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Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners
Sanderson et al.
Hum Mol Genet 2006;15:307-318.
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Early-onset ALS with long-term survival associated with spastin gene mutation
Meyer et al.
Neurology 2005;65:141-143.
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Beginning to Understand Hereditary Spastic Paraplegia Atlastin
Elliott
Arch Neurol 2004;61:1842-1843.
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Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia
Durr et al.
Arch Neurol 2004;61:1867-1872.
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Novel Mutation in the SPG3A Gene in an African American Family With an Early Onset of Hereditary Spastic Paraplegia
Hedera et al.
Arch Neurol 2004;61:1600-1603.
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Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon
Errico et al.
Hum Mol Genet 2004;13:2121-2132.
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Allan-Herndon-Dudley Syndrome: Should the Locus for This Hereditary Spastic Paraplegia Be Designated SPG 22?
Bohan and Azizi
Arch Neurol 2004;61:1470-1471.
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August 24 Highlight and Commentary
Neurology 2004;63:603-603.
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Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene
D'Amico et al.
Neurology 2004;62:2138-2139.
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Hereditary Spastic Paraplegia: Spastin Phenotype and Function
Fink and Rainier
Arch Neurol 2004;61:830-833.
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A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts
Orlacchio et al.
Neurology 2004;62:1875-1878.
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ARSACS goes global
Gomez
Neurology 2004;62:10-11.
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