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Molecular Genetics and Metabolism|January 7, 2014
Early initiation of enzyme replacement therapy for the mucopolysaccharidosesJoseph MuenzerJournal of Pediatric Rehabilitation Medicine|July 28, 2011
Evaluation of disease severity in mucopolysaccharidosesMichael Beck, Joseph Muenzer, Maurizio ScarpaPaediatric Respiratory Reviews|April 5, 2011
Respiratory manifestations in mucopolysaccharidosesMarianne S Muhlebach, William Wooten, Joseph MuenzerCase Reports in Dentistry|May 9, 2012
Idiopathic gingival hyperplasia: a case report with a 17-year followupBien Lai, Joseph Muenzer, Michael W RobertsPediatrics|January 2, 2009
Mucopolysaccharidosis I: management and treatment guidelinesJoseph Muenzer, James E Wraith, Lorne A Clarke, et al.The Journal of Gene Medicine|July 7, 2010
Restoration of central nervous system alpha-N-acetylglucosaminidase activity and therapeutic benefits in mucopolysaccharidosis IIIB mice by a single intracisternal recombinant adeno-associated viral type 2 vector deliveryHaiyan Fu, Julianne DiRosario, Lu Kang, et al.The Journal of Pediatrics|January 12, 2013
Relationship of sleep to pulmonary function in mucopolysaccharidosis IIWilliam I Wooten, Joseph Muenzer, Bradley V Vaughn, et al.Archives of Disease in Childhood|November 3, 2020
Improvement in time to treatment, but not time to diagnosis, in patients with mucopolysaccharidosis type IRoberto Giugliani, Nicole Muschol, Hillary A Keenan, et al.Molecular Genetics and Metabolism|November 20, 2025
Evaluation and follow-up of newborns screening positive for mucopolysaccharidosis II: Results from an international modified Delphi consensusBarbara K Burton, N Matthew Ellinwood, Katey K Hoffman, et al.Pageof 9