Hallervorden-Spatz Syndrome

Known as: Neuroaxonal Dystrophies, Juvenile-Onset, Dystrophies, Juvenile-Onset Neuroaxonal, Hallervorden Spatz Disease 
A rare autosomal recessive degenerative disorder which usually presents in late childhood or adolescence. Clinical manifestations include progressive… (More)
National Institutes of Health

Papers overview

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Highly Cited
2005
Highly Cited
2005
A growing body of evidence indicates that an inflammatory process in the substantia nigra, characterized by activation of… (More)
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Highly Cited
2003
Highly Cited
2003
BACKGROUND Hallervorden-Spatz syndrome is an autosomal recessive disorder characterized by dystonia, parkinsonism, and iron… (More)
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2002
2002
A young man presenting with a Tourette syndrome-like disorder that was the main clinical manifestation of Hallervorden-Spatz… (More)
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Highly Cited
2001
Highly Cited
2001
Hallervorden-Spatz syndrome (HSS) is an autosomal recessive neurodegenerative disorder associated with iron accumulation in the… (More)
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Review
2001
Review
2001
The dark discoloration of globus pallidus and substantia nigra pars reticularis in the Hallervorden-Spatz syndrome is due to the… (More)
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1996
1996
Hallervorden-Spatz syndrome (HSS) (OMIM #234200) is a rare, autosomal recessive neurodegenerative disorder with brain iron… (More)
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1993
1993
It is reported the case of a male patient with 19 years old presenting progressive behavior disturbance and dystonic posture… (More)
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Review
1991
Review
1991
Aberrant iron metabolism in the brain is typified by Hallervorden-Spatz syndrome. In this disorder, large amounts of iron are… (More)
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Highly Cited
1988
Highly Cited
1988
Two women with a presumptive diagnosis of Hallervorden-Spatz syndrome had a combination of dystonia and parkinsonism. One had… (More)
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1977
1977
Two siblings with Hallervorden-Spatz syndrome showed striking homotypism and homochronism. Neuropathologic examination and… (More)
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