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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Detaylı Bibliyografya
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1993
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Article
Online Erişim: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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