Neurological dysfunction represents a significant clinical component of many of the mucopolysaccharidoses (also known as MPS disorders). The accurate and consistent assessment of neuropsychological function is essential to gain a greater understanding of the precise natural history of these conditions and to design effective clinical trials to evaluate the impact of therapies on the brain. In 2017, an International MPS Consensus Panel published recommendations for best practice in the design and conduct of clinical studies investigating the effects of therapies on cognitive function and adaptive behavior in patients with neuronopathic mucopolysaccharidoses. Based on an International MPS Consensus Conference held in February 2020, this artic...
Introduction: Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is an autosomal recessive lysoso...
Abstract Mucopolysaccharidoses (MPS) are genetic, progressive, lysosomal storage disorders affecting...
Approximately two-thirds of patients with mucopolysaccharidosis II (MPS II; Hunter syndrome) have ne...
Abstract Mucopolysaccharidoses (MPS) are a group of lysosomal multisystemic, chronic, and progressiv...
Abstract Background Mucopolysaccharidosis type III is a progressive, neurodegenerative lysosomal sto...
AbstractThe design and conduct of clinical studies to evaluate the effects of novel therapies on cen...
Abstract The mucopolysaccharidosis (MPS) disorders are a group of rare, inherited lysosomal storage ...
Objective: To advance the prediction of the neurocognitive development in MPS II patients by jointly...
The need for long-lasting and transformative therapies for mucopolysaccharidoses (MPS) cannot be und...
Mucopolysaccharidosis type IIIA (MPS IIIA, also known as Sanfilippo syndrome) is a rare genetic lyso...
Mucopolysaccharidosis (MPS) disorders are caused by deficiencies in lysosomal enzymes, leading to im...
Purpose. Mucopolysaccharidoses (MPS) are group of inherited lysosomal storage diseases caused by mut...
Selva, Erica M.Mason, Robert W.Tomatsu, ShunjiMucopolysaccharidoses (MPS) are lysosomal storage diso...
Introduction: Mucopolysaccharidosis type III (MPS III) is a rare disorder characterized by progressi...
The mucopolysaccharidoses (MPS) are a subgroup of lysosomal storage disorders that are caused by mut...
Introduction: Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is an autosomal recessive lysoso...
Abstract Mucopolysaccharidoses (MPS) are genetic, progressive, lysosomal storage disorders affecting...
Approximately two-thirds of patients with mucopolysaccharidosis II (MPS II; Hunter syndrome) have ne...
Abstract Mucopolysaccharidoses (MPS) are a group of lysosomal multisystemic, chronic, and progressiv...
Abstract Background Mucopolysaccharidosis type III is a progressive, neurodegenerative lysosomal sto...
AbstractThe design and conduct of clinical studies to evaluate the effects of novel therapies on cen...
Abstract The mucopolysaccharidosis (MPS) disorders are a group of rare, inherited lysosomal storage ...
Objective: To advance the prediction of the neurocognitive development in MPS II patients by jointly...
The need for long-lasting and transformative therapies for mucopolysaccharidoses (MPS) cannot be und...
Mucopolysaccharidosis type IIIA (MPS IIIA, also known as Sanfilippo syndrome) is a rare genetic lyso...
Mucopolysaccharidosis (MPS) disorders are caused by deficiencies in lysosomal enzymes, leading to im...
Purpose. Mucopolysaccharidoses (MPS) are group of inherited lysosomal storage diseases caused by mut...
Selva, Erica M.Mason, Robert W.Tomatsu, ShunjiMucopolysaccharidoses (MPS) are lysosomal storage diso...
Introduction: Mucopolysaccharidosis type III (MPS III) is a rare disorder characterized by progressi...
The mucopolysaccharidoses (MPS) are a subgroup of lysosomal storage disorders that are caused by mut...
Introduction: Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is an autosomal recessive lysoso...
Abstract Mucopolysaccharidoses (MPS) are genetic, progressive, lysosomal storage disorders affecting...
Approximately two-thirds of patients with mucopolysaccharidosis II (MPS II; Hunter syndrome) have ne...