1.
Rev. esp. enferm. dig
; 111(2): 168-169, feb. 2019. ilus, tab
Article
in Spanish
| IBECS
| ID: ibc-182207
ABSTRACT
No disponible
Subject(s)
Humans , Male , Adult , Liver Cirrhosis/surgery , Glycogen Storage Disease/complications , Carcinoma, Hepatocellular/complications , Liver Transplantation
2.
Rev Esp Enferm Dig
; 111(2): 168-169, 2019 Feb.
Article
in English
| MEDLINE
| ID: mdl-30318896
ABSTRACT
Type III glycogen storage disease (GSD-III) is an autosomal recessive disorder due to the deficiency of the glycogen debrancher enzyme. 80% of the patients have hepatic and muscular involvement (IIIa), compared to 15% with only liver involvement (IIIb). As the life expectancy improves in these patients, the possible liver complications are better understood.
Subject(s)
Carcinoma, Hepatocellular/surgery , Glycogen Storage Disease Type III/surgery , Liver Cirrhosis/surgery , Liver Neoplasms/surgery , Liver Transplantation , Adult , Glycogen Storage Disease Type III/complications , Humans , Male , Middle Aged , Neoplasm Recurrence, Local
3.
Gastroenterol. hepatol. (Ed. impr.)
; 36(4): 271-273, abr. 2013. ilus, tab
Article
in Spanish
| IBECS
| ID: ibc-112085
4.
Gastroenterol Hepatol
; 36(4): 271-3, 2013 Apr.
Article
in Spanish
| MEDLINE
| ID: mdl-23453560