ASPA gene

Known as: AMINOACYLASE 2, ASPA, Canavan disease 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1971-2017
0519712017

Papers overview

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Highly Cited
2003
Highly Cited
2003
Current epileptic seizure "prediction" algorithms are generally based on the knowledge of seizure occurring time and analyze the… (More)
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Highly Cited
2002
Highly Cited
2002
This clinical protocol describes virus-based gene transfer for Canavan disease, a childhood leukodystrophy. Canavan disease, also… (More)
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2002
2002
Canavan disease is a devastating neurodegenerative childhood disease caused by mutations in aspartoacylase, an enzyme that… (More)
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2000
2000
With the ultimate goal of developing safe and effective in vivo gene therapy for the treatment of Canavan disease and other… (More)
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2000
2000
BACKGROUND Canavan disease (CD) is an autosomal recessive leukodystrophy characterized by deficiency of aspartoacylase (ASPA) and… (More)
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1996
1996
Canavan disease is inherited as an autosomal recessive trait that is caused by the deficiency of aspartoacylase (ASPA). The… (More)
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1994
1994
Canavan disease, or spongy degeneration of the brain, is a severe leukodystrophy caused by the deficiency of aspartoacylase (ASPA… (More)
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1991
1991
Canavan disease, an autosomal recessive disorder, is characterized biochemically by N-acetylaspartic aciduria and aspartoacylase… (More)
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Highly Cited
1988
Highly Cited
1988
An increased amount of N-acetylaspartic acid was found in urine and plasma of three patients, from two families, with the… (More)
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1977
1977
  • L Forsten
  • Scandinavian journal of dental research
  • 1977
The release of fluoride from a glass ionomer cement (ASPA) was compared with that from a silicate cement. Test specimens were… (More)
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