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Biologics : Targets & Therapy|August 27, 2009
Review of the use of idursulfase in the treatment of mucopolysaccharidosis IIT Andrew Burrow, Nancy D LesliePediatric Neurology|May 18, 2010
Acute progression of neuromuscular findings in infantile Pompe diseaseT Andrew Burrow, Laurie A Bailey, Douglas G Kinnett, et al.Current Opinion in Pediatrics|November 21, 2007
Enzyme reconstitution/replacement therapy for lysosomal storage diseasesT Andrew Burrow, Robert J Hopkin, Nancy D Leslie, et al.European Journal of Human Genetics : EJHG|December 11, 2024
Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyriaAlexis N Roach, Hannah Barkley, Carissa Rodriquez, et al.Molecular Genetics and Metabolism|January 24, 2018
Correlating liver stiffness with disease severity scoring system (DS3) values in Gaucher disease type 1 (GD1) patientsSuraj D Serai, Anjani P Naidu, T Andrew Burrow, et al.The Journal of Pediatrics|January 24, 2007
Gaucher disease: progressive mesenteric and mediastinal lymphadenopathy despite enzyme therapyT Andrew Burrow, Mitchell B Cohen, Ronald Bokulic, et al.Archives of Otolaryngology--Head & Neck Surgery|June 17, 2009
Characterization of congenital anomalies in individuals with choanal atresiaT Andrew Burrow, Howard M Saal, Alessandro de Alarcon, et al.Texas Heart Institute Journal|December 26, 2017
Widespread Vasculopathy in a Patient with Morquio A SyndromeAdam W Powell, Michael D Taylor, T Andrew Burrow, et al.The Journal of Pediatrics|July 26, 2011
Cardiac disease in methylmalonic acidemiaCarlos E Prada, Fatma Al Jasmi, Edwin P Kirk, et al.Pediatric Neurology|January 29, 2019
CNTNAP1-Related Congenital Hypomyelinating NeuropathyHarry Lesmana, Marissa Vawter Lee, Seyed Ali Hosseini, et al.Pageof 3