To use our experience with patients in the observational database HOS - the Hunter Outcome Survey - to evaluate the feasibility of home infusions of idursulfase for patients with mucopolysaccharidosis type II (MPS II)
Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a rare lysosomal storage dis...
A preliminary exploratory study shows solid agreement between the results of case reports and clinic...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is a rare, X-linked recessive multisystem ly...
To evaluate the occurrence of infusion-related reactions (IRRs) in patients with mucopolysaccharidos...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a life-limiting, multisystem...
Abstract Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a rare lysosomal st...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a rare lysosomal storage dis...
textabstractMucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive dis...
Abstract Background Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare, X-linked diso...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive disease caused ...
Abstract Background Mucopolysaccharidosis II (MPS II; Hunter syndrome) is a rare, life-limiting lyso...
Mucopolysaccharidosis type II (MPS II), or Hunter syndrome, is the hereditary lysosomal storage dise...
BackgroundMucopolysaccharidosis II (MPS II; Hunter syndrome) is a rare, life-limiting lysosomal stor...
Simona Sestito, Ferdinando Ceravolo, Michele Grisolia, Elisa Pascale, Licia Pensabene, Daniela Conco...
Hunter syndrome (Mucopolysaccharidosis type II, MPS II) is a rare X-linked disease caused by a de...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a rare lysosomal storage dis...
A preliminary exploratory study shows solid agreement between the results of case reports and clinic...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is a rare, X-linked recessive multisystem ly...
To evaluate the occurrence of infusion-related reactions (IRRs) in patients with mucopolysaccharidos...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a life-limiting, multisystem...
Abstract Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a rare lysosomal st...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a rare lysosomal storage dis...
textabstractMucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive dis...
Abstract Background Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare, X-linked diso...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive disease caused ...
Abstract Background Mucopolysaccharidosis II (MPS II; Hunter syndrome) is a rare, life-limiting lyso...
Mucopolysaccharidosis type II (MPS II), or Hunter syndrome, is the hereditary lysosomal storage dise...
BackgroundMucopolysaccharidosis II (MPS II; Hunter syndrome) is a rare, life-limiting lysosomal stor...
Simona Sestito, Ferdinando Ceravolo, Michele Grisolia, Elisa Pascale, Licia Pensabene, Daniela Conco...
Hunter syndrome (Mucopolysaccharidosis type II, MPS II) is a rare X-linked disease caused by a de...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome; OMIM 309900) is a rare lysosomal storage dis...
A preliminary exploratory study shows solid agreement between the results of case reports and clinic...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is a rare, X-linked recessive multisystem ly...