Spastic paraplegia 3, autosomal dominant

Known as: strumpell's disease, SPG3, Spastic Paraplegia 3 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1947-2018
051019472017

Papers overview

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Highly Cited
2010
Highly Cited
2010
Hereditary spastic paraplegias (HSPs; SPG1-45) are inherited neurological disorders characterized by lower extremity spastic… (More)
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Highly Cited
2009
Highly Cited
2009
A population-based, cross-sectional study was performed in southeast Norway, between January 2002 and February 2008, to identify… (More)
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2008
2008
Mutations in the SPG4 gene (spastin) and in the SPG3A gene (atlastin) account for the majority of 'pure' autosomal dominant form… (More)
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2007
2007
OBJECTIVE To study the frequency and distribution of mutations in SPG3A in a large cohort of patients with hereditary spastic… (More)
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2006
2006
BACKGROUND Hereditary spastic paraplegia (HSP) is a genetically heterogeneous neurodegenerative disease. The most frequent cause… (More)
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Highly Cited
2006
Highly Cited
2006
The pure hereditary spastic paraplegias (HSPs) are a group of conditions in which there is a progressive length-dependent… (More)
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2006
2006
Sirs, SPG6 is an autosomal dominant (AD) form of hereditary spastic paraplegia (HSP), a clinically and genetically heterogeneous… (More)
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2005
2005
Hereditary spastic paraplegia (HSP) is a genetically heterogeneous group of neurodegenerative disorders characterized by… (More)
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2004
2004
Hereditary spastic paraplegia (HSP) is a group of neurodegenerative disorders mainly characterized by progressive spasticity of… (More)
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1996
1996
We report the clinical features of 12 families with autosomal dominant spastic paraplegia (ADSP) linked to the SPG4 locus on… (More)
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