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ALPHA-D-GALACTOSIDASE ENZYME

Known as: alpha Galactosidases, ALPHA-GALACTOSIDASE, alpha-Galactosidase A 
An enzyme that catalyzes the hydrolysis of terminal, non-reducing alpha-D-galactose residues in alpha-galactosides including galactose… Expand
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
Fabry disease is an X-linked lysosomal storage disease caused by deficiency of α-galactosidase A that affects males and shows… Expand
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Unexplained left ventricular hypertrophy often prompts the diagnosis of hypertrophic cardiomyopathy, a sarcomere… Expand
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Strokes are an important cause of morbidity and mortality in young adults. However, in most cases the cause of the… Expand
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Highly Cited
2002
Highly Cited
2002
Background—Although studies have suggested that “late-onset” hypertrophic cardiomyopathy (HCM) may be caused by sarcomeric… Expand
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Fabry's disease, lysosomal alpha-galactosidase A deficiency, results from the progressive accumulation of… Expand
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Highly Cited
2001
Highly Cited
2001
CONTEXT Fabry disease is a metabolic disorder without a specific treatment, caused by a deficiency of the lysosomal enzyme alpha… Expand
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Highly Cited
1995
Highly Cited
1995
BACKGROUND Fabry's disease is considered very rare. Left ventricular hypertrophy is one of the common manifestations in adults… Expand
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Highly Cited
1993
Highly Cited
1993
Pig tissues were screened by immunofluorescence with lectins, mAb, and human natural antibodies for the presence of carbohydrate… Expand
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Highly Cited
1970
Highly Cited
1970
  • J. Kint
  • Science
  • 1970
  • Corpus ID: 28982704
The leukocytes of male patients with Fabry's disease are deficient in α-galactosidase. The α-galactosidase activity in the… Expand
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