Troyer syndrome

Known as: Cross-McKusick syndrome, Spastic paraplegia, autosomal recessive, Troyer type, SPG20 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1967-2018
012319672018

Papers overview

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2015
2015
UNLABELLED Early detection of the highly aggressive malignancy cholangiocarcinoma (CCA) remains a challenge but has the potential… (More)
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2012
2012
Hereditary spastic paraplegias (HSPs; SPG1-48) are inherited neurological disorders characterized by lower extremity spasticity… (More)
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2011
2011
The presence of cancer-specific DNA methylation patterns in epithelial colorectal cells in human feces provides the prospect of a… (More)
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2008
2008
BACKGROUND Hereditary spastic paraplegias (SPG1-SPG33) are characterized by progressive spastic weakness of the lower limbs. A… (More)
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2007
2007
Troyer syndrome is an autosomal recessive hereditary spastic paraplegia caused by mutation in the spartin (SPG20) gene, which… (More)
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2006
2006
Mutation of spartin (SPG20) underlies a complicated form of hereditary spastic paraplegia, a disorder principally defined by the… (More)
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2005
2005
The hereditary spastic paraplegias comprise a group of inherited neurological disorders in which the primary manifestation is… (More)
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2004
2004
Troyer syndrome, originally described in 1967 in an Old Order Amish population, is a complicated form of hereditary spastic… (More)
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2004
2004
Troyer syndrome, originally described in 1967 in an Old Order Amish population, is a complicated form of hereditary spastic… (More)
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Highly Cited
2002
Highly Cited
2002
Troyer syndrome (TRS) is an autosomal recessive complicated hereditary spastic paraplegia (HSP) that occurs with high frequency… (More)
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