[Glycogen storage disease]. 1977

S Tarui

UI MeSH Term Description Entries
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

S Tarui
January 1994, Ryoikibetsu shokogun shirizu,
S Tarui
September 1965, Proceedings of the Royal Society of Medicine,
S Tarui
April 1969, British medical journal,
S Tarui
January 1964, Advances in metabolic disorders,
S Tarui
January 1997, Ryoikibetsu shokogun shirizu,
S Tarui
December 1983, Nursing mirror,
S Tarui
January 1993, Nihon rinsho. Japanese journal of clinical medicine,
S Tarui
December 1944, Archives of disease in childhood,
S Tarui
October 1953, The Proceedings of the Institute of Medicine of Chicago,
S Tarui
January 1948, Bulletin. New England Medical Center Hospital,
Copied contents to your clipboard!