| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients. | Brain | 2007 | 1.25 |
| 2 | Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion. | Arch Neurol | 2003 | 1.00 |
| 3 | Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis. | J Neurol | 2009 | 0.96 |
| 4 | Camptocormia phenotype of FSHD: a clinical and MRI study on six patients. | J Neurol | 2010 | 0.86 |
| 5 | Only subtle cognitive deficits in non-bulbar amyotrophic lateral sclerosis patients. | J Neurol | 2005 | 0.83 |
| 6 | Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletion. | J Neurol | 2003 | 0.81 |
| 7 | MuSK-antibody positive pure ocular myasthenia gravis. | J Neurol | 2005 | 0.76 |
| 8 | Lactate production upon short-term non-ischemic forearm exercise in mitochondrial disorders and other myopathies. | J Neurol | 2006 | 0.75 |