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SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)

Known as: Spastic paraplegia 6, autosomal dominant, Familial Spastic Paraplegia, Autosomal Dominant, 3, Fsp3 
National Institutes of Health

Papers overview

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Review
2012
Review
2012
Hereditary spastic paraplegia (SPG) is a clinically and genetically heterogeneous group of neurodegenerative disorders that are… Expand
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2012
2012
Mutations in NIPA1 (non-imprinted in Prader–Willi/Angelman syndrome) have been described as a cause of autosomal dominant… Expand
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2011
2011
Background and purpose:  Hereditary spastic paraplegia (HSP) is a group of clinically and genetically heterogeneous… Expand
Highly Cited
2005
Highly Cited
2005
Hereditary spastic paraplegia (HSP) is a genetically heterogeneous group of neurodegenerative disorders characterized by… Expand
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Highly Cited
2005
Highly Cited
2005
Hereditary spastic paraplegia (HSP) is a neurodegenerative disease characterized by lower‐limb spasticity, hyperreflexia… Expand
Highly Cited
2004
Highly Cited
2004
We report the genomic localization by homozygosity mapping and the identification of a gene for a new form of non-syndromic… Expand
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Highly Cited
2003
Highly Cited
2003
The hereditary spastic paraplegias (HSPs) are genetically heterogeneous disorders characterized by progressive lower-extremity… Expand
1999
1999
Objective: To map the gene responsible for autosomal dominant pure hereditary spastic paraplegia (ADPHSP) in a large affected… Expand
1999
1999
Editor—The hereditary spastic paraplegias are characterised by progressive spasticity, predominantly affecting the lower limbs… Expand
1998
1998
Autosomal dominant familial spastic paraplegia (FSP) is a genetically heterogeneous neurodegenerative disorder displaying… Expand