Author:
von Loesch E. Thassilo,Bačinović Mustafa,Farwick Anna-Lena,Meinhardt Achim,Quast Oliver
Publisher
Springer Science and Business Media LLC
Reference7 articles.
1. https://www.dgm.org/muskelerkrankungen/mcardle-erkrankung. Zugegriffen: 23. Nov. 2022
2. De Castro M, Johnston J, Biesecker L (2015) Determining the prevalence of McArdle disease from gene frequency by analysis of next generation sequencing data. Genet Med 17(12):1002–1006
3. Hamadeh M, Nasrallah K, Ajami Z, Zeaiter R, Abbas L, Hamadeh S, Fares J (2021) Clinical presentation and management of severe acute renal failure in McArdle disease. Clin Med Res 19(2):90–93
4. Scalco R et al (2020) Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC). Orphanet J Rare Dis 2020(15):330
5. Quinlivan R, Martinuzzi A, Schoser B (2014) Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V). Cochrane Database Syst Rev 2014(11):CD3458