Výsledky vyhledávání - Wraith, Ed

The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK Autor Moore, David, Connock, Martin J, Wraith, Ed, Lavery, Christine

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

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Screening for medium chain acyl-CoA dehydrogenase deficiency has still not been evaluated Autor Tanner, Stuart, Sharrard, Mark, Cleary, Maureen, Walter, John, Wraith, Ed, Lee, Philip, Leonard, James, Morris, Andrew, McIntosh, Neil

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Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioning Autor Boelens, Jaap Jan, Aldenhoven, Mieke, Purtill, Duncan, Ruggeri, Annalisa, DeFor, Todd, Wynn, Robert, Wraith, Ed, Cavazzana-Calvo, Marina, Rovelli, Attilio, Fischer, Alain, Tolar, Jakub, Prasad, Vinod K., Escolar, Maria, Gluckman, Eliane, O’Meara, Anne, Orchard, Paul J., Veys, Paul, Eapen, Mary, Kurtzberg, Joanne, Rocha, Vanderson, Driscoll, Timothy A., Kurtzberg, Joanne, Landi, Daniel B., Martin, Paul L., Page, Kristin M., Parikh, Suhag H, Prasad, Vinod K.

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