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Liver transplantation for glycogen storage disease types I, III, and IV.
Matern D, Starzl TE, Arnaout W, Barnard J, Bynon JS, Dhawan A, Emond J, Haagsma EB, Hug G, Lachaux A, Smit GP, Chen YT. Matern D, et al. Eur J Pediatr. 1999 Dec;158 Suppl 2(Suppl 2):S43-8. doi: 10.1007/pl00014320. Eur J Pediatr. 1999. PMID: 10603098 Free PMC article. Review.
Glycogen storage disease (GSD) types I, III, and IV can be associated with severe liver disease. ...It remains to be evaluated, whether a genotype-phenotype correlation exists for GSD type IV, which may aid in the decision making.
Glycogen storage disease (GSD) types I, III, and IV can be associated with severe liver disease. ...It re
The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studies.
Moses SW, Parvari R. Moses SW, et al. Curr Mol Med. 2002 Mar;2(2):177-88. doi: 10.2174/1566524024605815. Curr Mol Med. 2002. PMID: 11949934 Review.
Glycogen storage disease type IV (GSD-IV), also known as Andersen disease or amylopectinosis (MIM 23250), is a rare autosomal recessive disorder caused by a deficiency of glycogen branching enzyme (GBE)
Glycogen storage disease type IV (GSD-IV), also known as Andersen disease or amylopectinosi