OBJECTIVE:To evaluate the efficacy and safety of IV laronidase for MPS I. METHODS:A systematic literature review was performed by searching the ClinicalTrials.gov, MEDLINE/PubMed, EMBASE, LILACS, and Cochrane Library databases, limited to clinical trials published until December 31, 2016. The first inclusion criterion was being a randomized controlled trial (RCT). If < five RCTs were identified, open-label and nonrandomized trials, controlled or uncontrolled (quasi-experimental), including ≥ five patients, and evaluating relevant outcomes defined a priori, would also be included. For meta-analysis, primary inferences were based on random-effects models. Assessment of article quality was performed in accordance with the GRADE criteria. The C...
Introduction: Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is an autosomal recessive lysoso...
Background. There are limited data on the efficacy of long-term enzyme replacement therapy (ERT) in ...
BackgroundMucopolysaccharidosis I (MPS IH) is a lysosomal storage disease treated with hematopoietic...
<div><p>Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disease caused by deficient a...
Mucopolysaccharidoses are a group of inherited metabolic diseases caused by the absence or deficienc...
Recombinant human alpha-L-iduronidase (Aldurazyme (R) laronidase) is approved as an enzyme replaceme...
ABSTRACT Objective: To report the stabilization of urinary glycosaminoglicans (GAG) excretion and ...
ObjectiveTo evaluate long-term outcomes of laronidase enzyme replacement therapy in patients with at...
Orphan medicinal products (OMPs) are often authorized based on pivotal phase II and III trials that ...
The lysosomal storage disorder (LSD) mucopolysaccharidosis type I (MPS I, McKusick 25280, Hurler syn...
Background: Enzyme replacement therapy (ERT) with laronidase (recombinant human alpha-L-iduronidase,...
Central nervous system manifestations of mucopolysaccharidosis type I (MPS I) such as cognitive impa...
A preliminary exploratory study shows solid agreement between the results of case reports and clinic...
The authors describe the first mother-infant pair to complete an on-going, prospective, open-label, ...
Vestronidase alfa is an enzyme replacement therapy for mucopolysaccharidosis VII (MPS VII). In this ...
Introduction: Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is an autosomal recessive lysoso...
Background. There are limited data on the efficacy of long-term enzyme replacement therapy (ERT) in ...
BackgroundMucopolysaccharidosis I (MPS IH) is a lysosomal storage disease treated with hematopoietic...
<div><p>Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disease caused by deficient a...
Mucopolysaccharidoses are a group of inherited metabolic diseases caused by the absence or deficienc...
Recombinant human alpha-L-iduronidase (Aldurazyme (R) laronidase) is approved as an enzyme replaceme...
ABSTRACT Objective: To report the stabilization of urinary glycosaminoglicans (GAG) excretion and ...
ObjectiveTo evaluate long-term outcomes of laronidase enzyme replacement therapy in patients with at...
Orphan medicinal products (OMPs) are often authorized based on pivotal phase II and III trials that ...
The lysosomal storage disorder (LSD) mucopolysaccharidosis type I (MPS I, McKusick 25280, Hurler syn...
Background: Enzyme replacement therapy (ERT) with laronidase (recombinant human alpha-L-iduronidase,...
Central nervous system manifestations of mucopolysaccharidosis type I (MPS I) such as cognitive impa...
A preliminary exploratory study shows solid agreement between the results of case reports and clinic...
The authors describe the first mother-infant pair to complete an on-going, prospective, open-label, ...
Vestronidase alfa is an enzyme replacement therapy for mucopolysaccharidosis VII (MPS VII). In this ...
Introduction: Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is an autosomal recessive lysoso...
Background. There are limited data on the efficacy of long-term enzyme replacement therapy (ERT) in ...
BackgroundMucopolysaccharidosis I (MPS IH) is a lysosomal storage disease treated with hematopoietic...