Hans H. Goebel

224th ENMC International Workshop:

Yves Allenbach, Andrew L. Mammen, Olivier Benvéniste et al. · Neuromuscular Disorders · 2017 · 526 citations · Full text

Enmc International Workshop, Global Challenge, Performance Studies +1

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

Kristen L. Nowak, Duangrurdee Wattanasirichaigoon, Hans H. Goebel et al. · Nature Genetics · 1999 · 398 citations

Muscle Physiology, Muscle Function, Health Sciences +11

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 · 335 citations · Full text

Apoptosis, Cell Death, Synaptic Signaling +23

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 · 250 citations · Full text

Arylsulfatase A, Pathology, Experimental Pathology +23

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

Kati Donner, Miina Ollikainen, Maaret Ridanpää et al. · Neuromuscular Disorders · 2002 · 225 citations

Rare Cause, Medicine, Molecular Biology +5