K. Eger

Distinct muscle imaging patterns in myofibrillar myopathies

Dirk Fischer, Rudolf A. Kley, Katharina Strach et al. · Neurology · 2008 · 252 citations · Full text

Enzyme replacement therapy with alglucosidase alfa in 44 patients with late-onset glycogen storage disease type 2: 12-month results of an observational clinical trial

S. Strothotte, N. Strigl‐Pill, Birgit Grunert et al. · Journal of Neurology · 2009 · 249 citations

Observational Clinical Trial, Enzyme Replacement Therapy, Inherited Metabolic Disease +4

Atypical Phenotypes in Patients With Facioscapulohumeral Muscular Dystrophy 4q35 Deletion

Michael Krasnianski, K. Eger, Stephan Neudecker et al. · Archives of Neurology · 2003 · 67 citations

Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis

Rubén Fernández‐Santiago, S. Hoenig, Peter Lichtner et al. · Journal of Neurology · 2009 · 65 citations · Full text

Camptocormia phenotype of FSHD: a clinical and MRI study on six patients

Berit Jordan, K. Eger, Sabrina Koesling et al. · Journal of Neurology · 2010 · 57 citations

Camptocormia Phenotype, Pathology, Neurology +3