textabstractBackground: Developments in enzyme replacement therapy have kindled discussions on adding Pompe disease, characterized by progressive muscle weakness and wasting, to neonatal screening. Pompe disease does not fit traditional screening criteria as it is a broad-spectrum phenotype disorder that may occur in lethal form in early infancy or manifest in less severe forms from infancy to late adulthood. Current screening tests cannot differentiate between these forms. Normally, expanding screening is discussed among experts in advisory bodies. While advisory reports usually mention the procedures and outcome of deliberations, little is known of the importance attached to different arguments and the actual weighing processes involved. ...
Pompe disease, also known as acid maltase deficiency or acid alpha-glucosidase deficiency, in its mo...
Pompe disease (glycogen storage disease type II or acid maltase deficiency) is a lysosomal disorder ...
: Pompe disease (PD) is a progressive neuromuscular disorder caused by a lysosomal acid α-glucosidas...
Background: Developments in enzyme replacement therapy have kindled discussions on adding Pompe dise...
Background: Neonatal screening for Pompe disease has been introduced in Taiwan and a few U. S. state...
Background: Neonatal screening for Pompe disease has been introduced in Taiwan and a few U.S. states...
© 2009 Yvette M. CurlisPompe disease is a rare autosomal recessive condition caused by a deficiency ...
BACKGROUND. Pompe disease is a lysosomal storage disorder that leads to the accumulation of glycogen...
Background: Newborn screening is a public health program to identify conditions associated with sign...
Introduction:Pompe disease is a lysosomal storage disorder caused by a deficiency in acid -glucosida...
Pompe disease was added to the United States recommended uniform screening panel in 2015 to avoid di...
Background:Newborn screening is a public health program to identify conditions associated with signi...
Pompe disease is an inherited lysosomal storage disorder caused by acid alpha-glucosidase (GAA) enzy...
OBJECTIVE: Pompe disease causes progressive, debilitating, and often life -threatening musculoskelet...
OBJECTIVE: Pompe disease is an autosomal recessive lysosomal storage disorder that is caused by defi...
Pompe disease, also known as acid maltase deficiency or acid alpha-glucosidase deficiency, in its mo...
Pompe disease (glycogen storage disease type II or acid maltase deficiency) is a lysosomal disorder ...
: Pompe disease (PD) is a progressive neuromuscular disorder caused by a lysosomal acid α-glucosidas...
Background: Developments in enzyme replacement therapy have kindled discussions on adding Pompe dise...
Background: Neonatal screening for Pompe disease has been introduced in Taiwan and a few U. S. state...
Background: Neonatal screening for Pompe disease has been introduced in Taiwan and a few U.S. states...
© 2009 Yvette M. CurlisPompe disease is a rare autosomal recessive condition caused by a deficiency ...
BACKGROUND. Pompe disease is a lysosomal storage disorder that leads to the accumulation of glycogen...
Background: Newborn screening is a public health program to identify conditions associated with sign...
Introduction:Pompe disease is a lysosomal storage disorder caused by a deficiency in acid -glucosida...
Pompe disease was added to the United States recommended uniform screening panel in 2015 to avoid di...
Background:Newborn screening is a public health program to identify conditions associated with signi...
Pompe disease is an inherited lysosomal storage disorder caused by acid alpha-glucosidase (GAA) enzy...
OBJECTIVE: Pompe disease causes progressive, debilitating, and often life -threatening musculoskelet...
OBJECTIVE: Pompe disease is an autosomal recessive lysosomal storage disorder that is caused by defi...
Pompe disease, also known as acid maltase deficiency or acid alpha-glucosidase deficiency, in its mo...
Pompe disease (glycogen storage disease type II or acid maltase deficiency) is a lysosomal disorder ...
: Pompe disease (PD) is a progressive neuromuscular disorder caused by a lysosomal acid α-glucosidas...