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SPASTIC PARAPLEGIA 2, X-LINKED (disorder)

Known as: SPASTIC PARAPLEGIA 2, X-LINKED, SPG2, SPPX2 
 
National Institutes of Health

Papers overview

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2014
2014
Background: Certain hereditary spastic paraplegia (HSP)-related proteins possess hairpin domains and regulate the morphology of… Expand
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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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Review
2012
Review
2012
The purpose of this article is to present contemporary information on the clinical and molecular diagnosis and the treatment of… Expand
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2010
2010
BACKGROUND AND PURPOSE These EFNS guidelines on the molecular diagnosis of neurogenetic disorders are designed to provide… Expand
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Review
2006
Review
2006
Abstract.Pelizaeus-Merzbacher disease (PMD) and the allelic spastic paraplegia type 2 (SPG2) arise from mutations in the X-linked… Expand
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2002
2002
X-linked hereditary spastic paraplegias (HSPs) present with two distinct phenotypes: pure and complicated. The pure form is… Expand
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1999
1999
Spastic paraplegia type 2 (SPG2) is allelic to Pelizaeus-Merzbacher disease (PMD), with both conditions resulting from mutations… Expand
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1996
1996
X-linked hereditary spastic paraplegias (HSP) present with two distinct phenotypes, pure and complicated. The pure form is… Expand
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Review
1996
Review
1996
Familial spastic paraplegia (FSP or SPG) is a genetically heterogeneous group of upper motor neuron syndromes. To date, two… Expand
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Highly Cited
1994
Highly Cited
1994
Three forms of X–linked spastic paraplegia (SPG) have been defined. One locus (SPG 1) maps to Xq28 while two clinically distinct… Expand
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