BIOMAT Database Logo BIOMAT Database Logo

[Glycogen storage disorders]. 1956

H ZELLWEGER

UI MeSH Term Description Entries
D006003 Glycogen
D006008 Glycogen Storage Disease A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement. Glycogenosis,Disease, Glycogen Storage,Diseases, Glycogen Storage,Glycogen Storage Diseases,Glycogenoses,Storage Disease, Glycogen,Storage Diseases, Glycogen
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

H ZELLWEGER
Glycogen metabolism and glycogen storage disorders.
December 2018, Annals of translational medicine,
H ZELLWEGER
The Glycogen Storage Disorders.
January 2020, Pediatrics in review,
H ZELLWEGER
Animal models of glycogen storage disorders.
January 2011, Progress in molecular biology and translational science,
H ZELLWEGER
Disorders of glycogen metabolism; with special reference to glycogen storage disease and galactosemia.
March 1952, Pediatrics,
H ZELLWEGER
Glycogen metabolism and glycogen-storage diseases.
October 1975, Physiological reviews,
H ZELLWEGER
[Glycogen storage disease].
January 1994, Ryoikibetsu shokogun shirizu,
H ZELLWEGER
Glycogen storage disease.
September 1965, Proceedings of the Royal Society of Medicine,
H ZELLWEGER
[Glycogen storage disease].
January 1977, Nihon rinsho. Japanese journal of clinical medicine,
H ZELLWEGER
Glycogen storage disease.
April 1969, British medical journal,
H ZELLWEGER
[Glycogen storage diseases].
June 1969, Saishin igaku. Modern medicine,
Copied contents to your clipboard!