Hans H. Goebel

224th ENMC International Workshop:

Yves Allenbach, Andrew L. Mammen, Olivier Benvéniste et al. · Neuromuscular Disorders · 2017 · 554 citations · Full text

Computing, Mechanical Engineering, Global Navigation Satellite Systems +1

Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

Duangrurdee Wattanasirichaigoon, Hans H. Goebel, Matthew C. J. Wilce et al. · Nature Genetics · 1999 · 401 citations

Medicine, Genetics, Molecular Genetics +13

Neuronal loss and brain atrophy in mice lacking cathepsins B and L

Ute Felbor, Benedikt M. Kessler, Walther Mothes et al. · Proceedings of the National Academy of Sciences · 2002 · 336 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

Phenotype of arylsulfatase A-deficient mice: Relationship to human metachromatic leukodystrophy

Paul Säftig, Dieter Hartmann, R. Coenen et al. · Proceedings of the National Academy of Sciences · 1996 · 260 citations · Full text

Medicine, Neurology, Neuroscience +17

Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

Kati Donner, Miina Ollikainen, Maaret Ridanpää et al. · Neuromuscular Disorders · 2002 · 226 citations

Medicine, Genetics, Molecular Genetics +13