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of 2
pro vyhledávání: '"Viviane Ederer"'
Autor:
Sven F. Garbade, Viviane Ederer, Peter Burgard, Udo Wendel, Ute Spiekerkoetter, Dorothea Haas, Sarah C. Grünert
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Abstract Background Glycogen storage disease type I (GSD I) is a rare autosomal recessive disorder of carbohydate metabolism characterized by recurrent hypoglycaemia and hepatomegaly. Management of GSD I is demanding and comprises a diet with defined
Externí odkaz:
https://doaj.org/article/69b9f93813504547987ea42901d7b116
Autor:
Dorothea Haas, Peter Burgard, Ute Spiekerkoetter, Sven F. Garbade, Sarah C. Grünert, Viviane Ederer, Udo Wendel
Background Glycogen storage disease type I (GSD I) is a rare autosomal recessive disorder of carbohydate metabolism characterized by recurrent hypoglycaemia and hepatomegaly. Management of GSD I is demanding and comprises a diet with defined carbohyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27ac418bc36dc1cc726723f37013cbcf
https://doi.org/10.21203/rs.3.rs-449981/v1
https://doi.org/10.21203/rs.3.rs-449981/v1