CHIMERISM AFTER LIVER TRANSPLANTATION FOR TYPE IV GLYCOGEN STORAGE DISEASE AND TYPE 1 GAUCHER’S DISEASE

BACKGROUND: Liver transplantation for type IV glycogen storage disease (branching-enzyme deficiency) results in the resorption of extrahepatic deposits of amylopectin, but the mechanism of resorption is not known. METHODS: We studied two patients with type IV glycogen storage disease 37 and 91 month...

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Main Authors: Starzl, Thomas E., Demetris, Anthony J., Trucco, Massimo, Ricordi, Camillo, Ildstad, Suzanne, Terasaki, Paul I., Murase, Noriko, Kendall, Ross S., Kocova, Mirjana, Rudert, William A., Zeevi, Adriana, Van Thiel, David
Format: Artigo
Language:Inglês
Published: 1993
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2963442/
https://ncbi.nlm.nih.gov/pubmed/8437594
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1056/NEJM199303183281101
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