Author:
Diekman Eugene F.,van der Pol W. Ludo,Nievelstein Rutger A. J.,Houten Sander M.,Wijburg Frits A.,Visser Gepke
Subject
Genetics(clinical),Genetics
Reference43 articles.
1. Adams EM, Chow CK, Premkumar A, Plotz PH (1995) The idiopathic inflammatory myopathies: spectrum of MR imaging findings. Radiographics 15:563–574
2. Andresen BS, Olpin S, Poorthuis BJ et al (1999) Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency. Am J Hum Genet 64:479–494. doi: 10.1086/302261
3. Bakermans AJ, Geraedts TR, van Weeghel M et al (2011) Fasting-induced myocardial lipid accumulation in long-chain acyl-CoA dehydrogenase knockout mice is accompanied by impaired left ventricular function. Circulation: Cardiovasc Imaging 4:558–565. doi: 10.1161/CIRCIMAGING.111.963751
4. Boneh A, Andresen BS, Gregersen N et al (2006) VLCAD deficiency: pitfalls in newborn screening and confirmation of diagnosis by mutation analysis. Mol Genet Metab 88:166–170. doi: 10.1016/j.ymgme.2005.12.012
5. Carlier R-Y, Laforêt P, Wary C et al (2011) Whole-body muscle MRI in 20 patients suffering from late onset Pompe disease: Involvement patterns. Neuromuscul Disord. doi: 10.1016/j.nmd.2011.06.748
Cited by
21 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