It has recently been announced that the Secretary of the U.S. Department of Health and Human Services has approved the recommendation by the Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC) to add mucopolysaccharidosis type II (MPS-II, Hunter Syndrome) to the recommended uniform screening panel (RUSP) in the United States [...
The mucopolysaccharidoses (MPS), Pompe Disease (PD), and Krabbe disease (KD) are inherited condition...
The mucopolysaccharidoses (MPSs) are a group of rare genetic disorders of glycosaminoglycan cataboli...
The mucopolysaccharidoses are a group of inherited disorders of lysosomal storage of glycosaminoglyc...
Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is an X-linked condition caus...
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases (LSDs) caused by an inherited...
Article is devoted to one of the orphan diseases — mucopolysaccharidosis (MPS), which is the result ...
There have been significant advances allowing for the integration of mucopolysaccharidosis I into ne...
PURPOSE: The US Secretary of Health and Human Services provides guidance to state newborn screening ...
The article presents a rare case of type II mucopolysaccharidosis (MPs) in children. From the age of...
textabstractMucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive dis...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive disease caused ...
Mucopolysaccharidoses (MPSs) are a class of lysosomal storage disorders resulting in progressive dis...
Mucopolysaccharidosis type II (MPS II), or Hunter syndrome, is the hereditary lysosomal storage dise...
There is a need to identify early disease markers to facilitate diagnosis of mucopolysaccharidosis t...
The aim of the study was to characterize clinically and biochemically mucopolysaccharidosis type II ...
The mucopolysaccharidoses (MPS), Pompe Disease (PD), and Krabbe disease (KD) are inherited condition...
The mucopolysaccharidoses (MPSs) are a group of rare genetic disorders of glycosaminoglycan cataboli...
The mucopolysaccharidoses are a group of inherited disorders of lysosomal storage of glycosaminoglyc...
Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is an X-linked condition caus...
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases (LSDs) caused by an inherited...
Article is devoted to one of the orphan diseases — mucopolysaccharidosis (MPS), which is the result ...
There have been significant advances allowing for the integration of mucopolysaccharidosis I into ne...
PURPOSE: The US Secretary of Health and Human Services provides guidance to state newborn screening ...
The article presents a rare case of type II mucopolysaccharidosis (MPs) in children. From the age of...
textabstractMucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive dis...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive disease caused ...
Mucopolysaccharidoses (MPSs) are a class of lysosomal storage disorders resulting in progressive dis...
Mucopolysaccharidosis type II (MPS II), or Hunter syndrome, is the hereditary lysosomal storage dise...
There is a need to identify early disease markers to facilitate diagnosis of mucopolysaccharidosis t...
The aim of the study was to characterize clinically and biochemically mucopolysaccharidosis type II ...
The mucopolysaccharidoses (MPS), Pompe Disease (PD), and Krabbe disease (KD) are inherited condition...
The mucopolysaccharidoses (MPSs) are a group of rare genetic disorders of glycosaminoglycan cataboli...
The mucopolysaccharidoses are a group of inherited disorders of lysosomal storage of glycosaminoglyc...