AbstractBackgroundMucopolysaccharidosis IVA (MPS IVA), or Morquio Syndrome type A, is an autosomal recessive disease caused by deficiency of the lysosomal enzyme N-acetylgalactosamine-6-sulfatase (GALNS), resulting in excessive lysosomal storage of keratan sulfate in many tissues and organs. This accumulation causes a severe skeletal dysplasia with short stature, and affects the eye, heart and other organs, with many signs and symptoms. Morquio A syndrome is estimated to occur in 1 in 200,000 to 300,000 live births. Clinical trials with enzyme replacement therapy for this disease are in progress, and it is probable that the treatment, when available, would be more effective if started early. We describe an innovative fluorometric method for...
Background: With ongoing efforts to develop improved treatments for Sanfilippo Syndrome Type A (MPS-...
The high frequency (3.3-3.9%) of acid a-glucosidase pseudodeficiency, c.[1726G > A; 2065G > A] homoz...
<p><b>A. Enzymatic GALNS assay in DBS</b> shows a statistically significant difference (p<0.0001 in ...
<div><p>Background</p><p>Mucopolysaccharidosis IVA (MPS IVA; Morquio A disease) is an autosomal rece...
Mucopolysaccharidosis type IVA or Morquio type-A disease is a hereditary lysosomal storage disorder ...
Background Mucopolysaccharidosis IVA (MPS IVA; Morquio A disease) is an autosomal recessive disease ...
Background: Mucopolysaccharidosis type IVA, also known as Morquio A or MPS IV A, is an autosomal rec...
Background:Mucopolysaccharidosis type II (MPS II) is a lysosomal storage disorder related to a defic...
Copyright © 2006 American Association for Clinical Chemistry, Inc.BackgroundMucopolysaccharidosis ty...
Copyright © 2005 Federation of European Biochemical Societies Published by Elsevier B.V.BackgroundMu...
Background: Mucopolysaccharidosis type I (MPS I) is caused by a deficiency of the alpha-L-iduronidas...
Copyright © 2006 Elsevier B.V. All rights reserved.BackgroundMucopolysaccharidosis type IVA (MPS IVA...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage ...
Objectives: Mucopolysaccharidosis II (MPS II), or Hunter Syndrome, is a lysosomal storage disorder t...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage ...
Background: With ongoing efforts to develop improved treatments for Sanfilippo Syndrome Type A (MPS-...
The high frequency (3.3-3.9%) of acid a-glucosidase pseudodeficiency, c.[1726G > A; 2065G > A] homoz...
<p><b>A. Enzymatic GALNS assay in DBS</b> shows a statistically significant difference (p<0.0001 in ...
<div><p>Background</p><p>Mucopolysaccharidosis IVA (MPS IVA; Morquio A disease) is an autosomal rece...
Mucopolysaccharidosis type IVA or Morquio type-A disease is a hereditary lysosomal storage disorder ...
Background Mucopolysaccharidosis IVA (MPS IVA; Morquio A disease) is an autosomal recessive disease ...
Background: Mucopolysaccharidosis type IVA, also known as Morquio A or MPS IV A, is an autosomal rec...
Background:Mucopolysaccharidosis type II (MPS II) is a lysosomal storage disorder related to a defic...
Copyright © 2006 American Association for Clinical Chemistry, Inc.BackgroundMucopolysaccharidosis ty...
Copyright © 2005 Federation of European Biochemical Societies Published by Elsevier B.V.BackgroundMu...
Background: Mucopolysaccharidosis type I (MPS I) is caused by a deficiency of the alpha-L-iduronidas...
Copyright © 2006 Elsevier B.V. All rights reserved.BackgroundMucopolysaccharidosis type IVA (MPS IVA...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage ...
Objectives: Mucopolysaccharidosis II (MPS II), or Hunter Syndrome, is a lysosomal storage disorder t...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage ...
Background: With ongoing efforts to develop improved treatments for Sanfilippo Syndrome Type A (MPS-...
The high frequency (3.3-3.9%) of acid a-glucosidase pseudodeficiency, c.[1726G > A; 2065G > A] homoz...
<p><b>A. Enzymatic GALNS assay in DBS</b> shows a statistically significant difference (p<0.0001 in ...