V42. De novo mutations in the FUS gene are a frequent cause of sporadic ALS in very young patients by Hübers, A, Volk, A, Just, W, Rosenbohm, A, Bierbaumer, N, Kathrin, M, Nicolai, M, Ingrid, G, Josef, H, Janine, A, Holger, T, Nürnberg, P, Weishaupt, J.H, Kubisch, C, Ludolph, A.C

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Contribution of caspase-8 to apoptosis of axotomized rat retinal ganglion cells in vivo by Weishaupt, J.H, Diem, R, Kermer, P, Krajewski, S, Reed, J.C, Bähr, M

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Neuron-specific overexpression of the co-chaperone Bcl-2-associated athanogene-1 in superoxide dismutase 1G93A –transgenic mice by Rohde, G, Kermer, P, Reed, J.C, Bähr, M, Weishaupt, J.H

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Genetische Diagnostik der amyotrophen Lateralsklerose by Weydt, P., Hübers, A., Ludolph, A.C., Weishaupt, J.H.

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Neuron-specific overexpression of the co-chaperone Bcl-2-associated athanogene-1 in superoxide dismutase 1 G93A–transgenic mice by Rohde, G., Kermer, P., Reed, J.C., Bähr, M., Weishaupt, J.H.

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Genetik der amyotrophen Lateralsklerose by Hübers, A., Weishaupt, J.H., Ludolph, A.C.

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Genetische Diagnostik der amyotrophen Lateralsklerose: Neue Aspekte by Weydt, P., Hübers, A., Ludolph, A.C., Weishaupt, J.H.

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The superoxide dismutase1 (sod1) G93A mutation does not promote neuronal injury after focal brain ischemia and optic nerve transection in mice by Kilic, E., Weishaupt, J.H., Kilic, Ü., Rohde, G., Yulug, B., Peters, K., Hermann, D.M., Bähr, M.

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