Publications by authors named "E D Wraith"

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Assessment of musculoskeletal abnormalities in children with mucopolysaccharidoses using pGALS.
Mercedes O Chan, Ethan S Sen, Elizabeth Hardy, Pauline Hensman, Edmond Wraith

Pediatr Rheumatol Online J· May 2015

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Does the timing of treatment affect the ocular phenotype in patients with Mucopolysaccharidosis I homozygous for the L490P mutation?
W H Chan, S Biswas, I C Lloyd, E Wraith, S Jones

Eye (Lond)· September 2013

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A Large Intragenic Deletion in the ACADM Gene Can Cause MCAD Deficiency but is not Detected on Routine Sequencing.
Claire Searle, Brage Storstein Andresen, Ed Wraith, Jamie Higgs, Deborah Gray

JIMD Rep· August 2013

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Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioning.
Jaap Jan Boelens, Mieke Aldenhoven, Duncan Purtill, Annalisa Ruggeri, Todd Defor, Ed Wraith

Blood· May 2013

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Source document verification in the Mucopolysaccharidosis Type I Registry.
Karien Verhulst, Laura Artiles-Carloni, Michael Beck, Joe T R Clarke, Jordao Correa Neto, Edward J Wraith

Pharmacoepidemiol Drug Saf· July 2012

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