Overview of the mucopolysaccharidoses

Idursulfase treatment of Hunter syndrome in children younger than 6 years: Results from the Hunter Outcome Survey

(2011) Joseph Muenzer et al.   GENETICS IN MEDICINE

A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis

(2011) Lisa Imundo et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: A perspective from the Hunter Outcome Survey (HOS)

(2011) Barbara K. Burton et al.   MOLECULAR GENETICS AND METABOLISM

Mucopolysaccharidosis type IIIA: Clinical spectrum and genotype-phenotype correlations

(2010) Marlies J. Valstar et al.   ANNALS OF NEUROLOGY

Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation

(2010) Kazuko Sukegawa et al.   CLINICAL GENETICS

Importance of surgical history in diagnosing mucopolysaccharidosis type II (Hunter syndrome): Data from the Hunter Outcome Survey

(2010) Nancy J. Mendelsohn et al.   GENETICS IN MEDICINE

Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome

(2010) Joseph Muenzer et al.   GENETICS IN MEDICINE

Effects of enzyme replacement therapy on growth in patients with mucopolysaccharidosis type II

(2010) G. Schulze-Frenking et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Mucopolysaccharidosis VI

(2010) Vassili Valayannopoulos et al.   Orphanet Journal of Rare Diseases

Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age-a sibling control study

(2009) JJ McGill et al.   CLINICAL GENETICS

Characterization of Surgical Procedures in Patients with Mucopolysaccharidosis Type I: Findings from the MPS I Registry

(2009) Pamela Arn et al.   JOURNAL OF PEDIATRICS

Transplant Outcomes in Mucopolysaccharidoses

(2009) Vinod K. Prasad et al.   SEMINARS IN HEMATOLOGY

Intrathecal enzyme replacement therapy in a patient with mucopolysaccharidosis type I and symptomatic spinal cord compression

(2008) Maria-Veronica Munoz-Rojas et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The controversial and changing role of haematopoietic cell transplantation for lysosomal storage disorders: an update

(2008) A M Rovelli   BONE MARROW TRANSPLANTATION

Recognition and Diagnosis of Mucopolysaccharidosis II (Hunter Syndrome)

(2008) R. Martin et al.   PEDIATRICS

Long-term Efficacy and Safety of Laronidase in the Treatment of Mucopolysaccharidosis I

(2008) L. A. Clarke et al.   PEDIATRICS

Mucopolysaccharidosis I: Management and Treatment Guidelines

(2008) J. Muenzer et al.   PEDIATRICS