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	1.	Limited effects of glatiramer acetate in the high-copy number hSOD1-G93A mouse model of ALS. [electronic resource] by Habisch, Hans-Jörg Schwalenstöcker, Birgit Danzeisen, Ruth Neuhaus, Oliver Hartung, Hans-Peter Ludolph, Albert Producer: 20070921 In: Experimental neurology vol. 206 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Tau isoforms expression in transgenic mouse model of amyotrophic lateral sclerosis. [electronic resource] by Usarek, Ewa Kuźma-Kozakiewicz, Magdalena Schwalenstöcker, Birgit Kaźmierczak, Beata Münch, Christoph Ludolph, Albert C Barańczyk-Kuźma, Anna Producer: 20070322 In: Neurochemical research vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Age-related changes in tau expression in transgenic mouse model of amyotrophic lateral sclerosis. [electronic resource] by Barańczyk-Kuźma, Anna Usarek, Ewa Kuźma-Kozakiewcz, Magdalena Kaźmierczak, Beata Gajewska, Beata Schwalenstocker, Birgit Ludolph, Albert C Producer: 20070801 In: Neurochemical research vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1. [electronic resource] by Fergani, Anissa Eschbach, Judith Oudart, Hugues Larmet, Yves Schwalenstocker, Birgit Ludolph, Albert C Loeffler, Jean-Philippe Dupuis, Luc Producer: 20110714 In: Molecular neurodegeneration vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Differential regulation of 5' splice variants of the glutamate transporter EAAT2 in an in vivo model of chemical hypoxia induced by 3-nitropropionic acid. [electronic resource] by Münch, Christoph Zhu, Bing-Gen Leven, Annette Stamm, Stefan Einkörn, Hermann Schwalenstöcker, Birgit Ludolph, Albert C Riepe, Matthias W Meyer, Thomas Producer: 20030507 In: Journal of neuroscience research vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease. [electronic resource] by Dupuis, Luc Fergani, Anissa Braunstein, Kerstin E Eschbach, Judith Holl, Nathalie Rene, Frédérique Gonzalez De Aguilar, Jose-Luis Zoerner, Björn Schwalenstocker, Birgit Ludolph, Albert C Loeffler, Jean-Philippe Producer: 20090408 In: Experimental neurology vol. 215 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Neuroprotective function of cellular prion protein in a mouse model of amyotrophic lateral sclerosis. [electronic resource] by Steinacker, Petra Hawlik, Andreas Lehnert, Stefan Jahn, Olaf Meier, Stephen Görz, Evamaria Braunstein, Kerstin E Krzovska, Marija Schwalenstöcker, Birgit Jesse, Sarah Pröpper, Christian Böckers, Tobias Ludolph, Albert Otto, Markus Producer: 20100607 In: The American journal of pathology vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation. [electronic resource] by Rona-Voros, Krisztina Eschbach, Judith Vernay, Aurélia Wiesner, Diana Schwalenstocker, Birgit Geniquet, Pauline Mousson De Camaret, Bénédicte Echaniz-Laguna, Andoni Loeffler, Jean-Philippe Ludolph, Albert C Weydt, Patrick Dupuis, Luc Producer: 20140708 In: Human molecular genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues. [electronic resource] by Eschbach, Judith Fergani, Anissa Oudart, Hugues Robin, Jean-Patrice Rene, Frédérique Gonzalez de Aguilar, Jose-Luis Larmet, Yves Zoll, Joffrey Hafezparast, Majid Schwalenstocker, Birgit Loeffler, Jean-Philippe Ludolph, Albert C Dupuis, Luc Producer: 20110307 In: Biochimica et biophysica acta vol. 1812 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis. [electronic resource] by Eschbach, Judith Schwalenstöcker, Birgit Soyal, Selma M Bayer, Hanna Wiesner, Diana Akimoto, Chizuru Nilsson, Ann-Charloth Birve, Anna Meyer, Thomas Dupuis, Luc Danzer, Karin M Andersen, Peter M Witting, Anke Ludolph, Albert C Patsch, Wolfgang Weydt, Patrick Producer: 20140219 In: Human molecular genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Guidelines for preclinical animal research in ALS/MND: A consensus meeting. [electronic resource] by Ludolph, Albert C Bendotti, Caterina Blaugrund, Eran Chio, Adriano Greensmith, Linda Loeffler, Jean-Philippe Mead, Richard Niessen, Heiko G Petri, Susanne Pradat, Pierre-Francois Robberecht, Wim Ruegg, Markus Schwalenstöcker, Birgit Stiller, Detlev van den Berg, Leonard Vieira, Fernando von Horsten, Stephan Producer: 20100802 In: Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	The dynactin p150 subunit: cell biology studies of sequence changes found in ALS/MND and Parkinsonian syndromes. [electronic resource] by Stockmann, Marianne Meyer-Ohlendorf, Marie Achberger, Kevin Putz, Stefan Demestre, Maria Yin, Haishan Hendrich, Corinna Linta, Leonhard Heinrich, Jutta Brunner, Cornelia Proepper, Christian Kuh, Georges F Baumann, Bernd Langer, Torben Schwalenstöcker, Birgit Braunstein, Kerstin E von Arnim, Christine Schneuwly, Stephan Meyer, Thomas Wong, Philip C Boeckers, Tobias M Ludolph, Albert C Liebau, Stefan Producer: 20131105 In: Journal of neural transmission (Vienna, Austria : 1996) vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons. [electronic resource] by Braunstein, Kerstin E Eschbach, Judith Ròna-Vörös, Krisztina Soylu, Rana Mikrouli, Elli Larmet, Yves René, Frédérique Gonzalez De Aguilar, Jose-Luis Loeffler, Jean-Philippe Müller, Hans-Peter Bucher, Selina Kaulisch, Thomas Niessen, Heiko G Tillmanns, Julia Fischer, Kristina Schwalenstöcker, Birgit Kassubek, Jan Pichler, Bernd Stiller, Detlef Petersen, Asa Ludolph, Albert C Dupuis, Luc Producer: 20110217 In: Human molecular genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)