A juvenile variant of glycogenosis IV (Anderse... [Eur J Pediatr. 1986] - PubMed

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A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease. [Hepatology. 1988]
A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease.
Greene HL, Brown BI, McClenathan DT, Agostini RM Jr, Taylor SR. Hepatology. 1988 Mar-Apr; 8(2):302-6.
[A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)]. [Arch Fr Pediatr. 1981]
[A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)].
Scotto JM, de Barsy T, Hadchouel M, Bernard O. Arch Fr Pediatr. 1981 Dec; 38 Suppl 1:837-41.
Type IV glycogen-storage disease. Light-microscopic, electron-microscopic, and enzymatic study. [Am J Clin Pathol. 1976]
Type IV glycogen-storage disease. Light-microscopic, electron-microscopic, and enzymatic study.
Bannayan GA, Dean WJ, Howell RR. Am J Clin Pathol. 1976 Oct; 66(4):702-9.
Review [Glycogenosis type IV (branching enzyme deficiency, amylopectinosis, Andersen disease, polyglucosan body disease)]. [Ryoikibetsu Shokogun Shirizu. ...]
Review [Glycogenosis type IV (branching enzyme deficiency, amylopectinosis, Andersen disease, polyglucosan body disease)].
Inui K. Ryoikibetsu Shokogun Shirizu. 1998; (18 Pt 1):43-4.
Review Glycogen metabolism and glycogen-storage diseases. [Physiol Rev. 1975]
Review Glycogen metabolism and glycogen-storage diseases.
Huijing F. Physiol Rev. 1975 Oct; 55(4):609-58.

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Cited by 3 PubMed Central articles

Hepatocellular carcinoma in glycogen storage disease type IV. [Arch Dis Child. 2000]
Hepatocellular carcinoma in glycogen storage disease type IV.
de Moor RA, Schweizer JJ, van Hoek B, Wasser M, Vink R, Maaswinkel-Mooy PD. Arch Dis Child. 2000 Jun; 82(6):479-80.
Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene. [J Clin Invest. 1996]
Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.
Bao Y, Kishnani P, Wu JY, Chen YT. J Clin Invest. 1996 Feb 15; 97(4):941-8.
Liver transplantation for type IV glycogen storage disease. [N Engl J Med. 1991]
Liver transplantation for type IV glycogen storage disease.
Selby R, Starzl TE, Yunis E, Brown BI, Kendall RS, Tzakis A. N Engl J Med. 1991 Jan 3; 324(1):39-42.

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A juvenile variant of glycogenosis IV (Andersen disease).
A juvenile variant of glycogenosis IV (Andersen disease).
Eur J Pediatr. 1986 Aug ;145(3):179-81.

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A juvenile variant of glycogenosis IV (Andersen disease).

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