Evolución de dos pacientes con síndrome de Hurler en tratamiento con enzima recombinante humana α-L-iduronidasa
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
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3. Identification and molecular characterization of α-L-iduronidase mutations present in mucopolysaccharidosis type I undergoing enzyme replacement therapy;Yogalingam;Hum Mutat,2004
4. Alpha-L-iduronidase premature stop codons and potential reathrough in mucopolysaccharidosis type I patients;Hein;J Mol Biol,2004
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1. The impact of laronidase treatment in otolaryngological manifestations of patients with mucopolysaccharidosis;Brazilian Journal of Otorhinolaryngology;2016-09
2. Ostéochondrodysplasies;Imagerie Musculosquelettique : Pathologies Générales;2013
3. Mucopolisacaridosis de tipo I Hurler: Informe de un caso;Archivos Argentinos de Pediatria;2012-10-01
4. Enzyme replacement therapy for mucopolysaccharidosis I: laronidase;Pediatric Health;2010-04
5. Guidelines for the Management of Mucopolysaccharidosis Type I;The Journal of Pediatrics;2009-10
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