Items where Author is "Hench, J."

Article

Oettinghaus, Bjorn and Schulz, J. M. and Restelli, L. M. and Licci, M. and Savoia, C. and Schmidt, Alexander and Schmitt, K. and Grimm, A. and Morè, L. and Hench, J. and Tolnay, M. and Eckert, A. and D'Adamo, P. and Franken, P. and Ishihara, N. and Mihara, K. and Bischofberger, J. and Scorrano, L. and Frank, Stephan. (2016) Synaptic dysfunction, memory deficits and hippocampal atrophy due to ablation of mitochondrial fission in adult forebrain neurons. Cell death and differentiation, 23 (1). pp. 18-28.

Probstel, A. K. and Schaller, A. and Lieb, J. and Hench, J. and Frank, S. and Fuhr, P. and Kappos, L. and Sinnreich, M.. (2016) Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimic. Neurol Genet, 2 (6). e121.

Ackema, K. B. and Hench, J. and Böckler, S. and Wang, S. C. and Sauder, U. and Mergentaler, H. and Westermann, B. and Bard, F. and Frank, S. and Spang, A.. (2014) The small GTPase Arf1 modulates mitochondrial morphology and function. The EMBO Journal, 33 (22). pp. 2659-2675.

Leu, S. and von Felten, S. and Frank, S. and Vassella, E. and Vajtai, I. and Taylor, E. and Schulz, M. and Hutter, G. and Hench, J. and Schucht, P. and Boulay, J. L. and Mariani, L.. (2013) IDH/MGMT-driven molecular classification of low-grade glioma is a strong predictor for long-term survival. Neuro-oncology, Vol. 15, H. 4. pp. 469-479.

Peyer, A. K. and Kinter, J. and Hench, J. and Frank, S. and Fuhr, P. and Thomann, S. and Fischmann, A. and Kneifel, S. and Camano, P. and Munain, A. L. and Sinnreich, M. and Renaud, S.. (2013) Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia. Neuromuscular disorders, Vol. 23, H. 2. pp. 149-154.