Andreas Hahn

Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

Jan Senderek, Carsten Bergmann, Claudia Stendel et al. · The American Journal of Human Genetics · 2003 · 210 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mendelian Disorder +9

Clinical implications of maximal respiratory pressure determinations for individuals with duchenne muscular dystrophy

Andreas Hahn, John R. Bach, Anne Delaubier et al. · Archives of Physical Medicine and Rehabilitation · 1997 · 151 citations

Clinical Implications, Kinesiology, Clinical Physiology +7

Evaluation of Children with SMA Type 1 Under Treatment with Nusinersen within the Expanded Access Program in Germany

Astrid Pechmann, Thorsten Langer, David Schorling et al. · Journal of Neuromuscular Diseases · 2018 · 144 citations · Full text

Recessive TRAPPC11 Mutations Cause a Disease Spectrum of Limb Girdle Muscular Dystrophy and Myopathy with Movement Disorder and Intellectual Disability

Nina Bögershausen, Nassim Shahrzad, Jessica X. Chong et al. · The American Journal of Human Genetics · 2013 · 118 citations · Full text

Genetic Disorder, Medicine, Genetics +5

47 patients with FLNA associated periventricular nodular heterotopia

Max Lange, Burkhard S. Kasper, Axel Bohring et al. · Orphanet Journal of Rare Diseases · 2015 · 105 citations · Full text