Author:
Nolte Kay W.,Janecke Andreas R.,Vorgerd Matthias,Weis Joachim,Schröder J. Michael
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine
Reference50 articles.
1. Agamanolis DP, Askari AD, Di Mauro S, Hays A, Kumar K, Lipton M et al (1980) Muscle phosphofructokinase deficiency: two cases with unusual polysaccharide accumulation and immunologically active enzyme protein. Muscle Nerve 3:456–467. doi: 10.1002/mus.880030602
2. Akman HO, Karadimas C, Gyftodimou Y, Grigoriadou M, Kokotas H, Konstantinidou A et al (2006) Prenatal diagnosis of glycogen storage disease type IV. Prenat Diagn 26:951–955. doi: 10.1002/pd.1533
3. Alegria A, Martins E, Dias M, Cunha A, Cardoso ML, Maire I (1999) Glycogen storage disease type IV presenting as hydrops fetalis. J Inherit Metab Dis 22:330–332. doi: 10.1023/A:1005568507267
4. Andersen DH (1950) Studies on glycogen disease with report of a case in which the glycogen was abnormal. In: Najjar VA (ed) Carbohydrate metabolism. John Hopkins Press, Baltimore, pp 28–42
5. Assereto S, van Diggelen OP, Diogo L, Morava E, Cassandrini D, Carreira I et al (2007) Null mutations and lethal congenital form of glycogen storage disease type IV. Biochem Biophys Res Commun 361:445–450. doi: 10.1016/j.bbrc.2007.07.074
Cited by
38 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献