Your search returned 25 results.

Results
	1.	Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutation. [electronic resource] by Türk, Matthias Wehnert, Manfred Schröder, Rolf Chevessier, Frédéric Producer: 20140213 In: Neuromuscular disorders : NMD vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The neuromuscular junction: selective remodeling of synaptic regulators at the nerve/muscle interface. [electronic resource] by Witzemann, Veit Chevessier, Frédéric Pacifici, Pier Giorgio Yampolsky, Pessah Producer: 20131223 In: Mechanisms of development vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Atypical nuclear abnormalities in a patient with Brody disease. [electronic resource] by Mussini, Jean-Marie Magot, Armelle Hantaï, Daniel Sternberg, Damien Chevessier, Frédéric Péréon, Yann Producer: 20160613 In: Neuromuscular disorders : NMD vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions. [electronic resource] by Chevessier, Frédéric Girard, Emmanuelle Molgó, Jordi Bartling, Sönke Koenig, Jeanine Hantaï, Daniel Witzemann, Veit Producer: 20081117 In: Human molecular genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A new mouse model for the slow-channel congenital myasthenic syndrome induced by the AChR εL221F mutation. [electronic resource] by Chevessier, Frédéric Peter, Christoph Mersdorf, Ulrike Girard, Emmanuelle Krejci, Eric McArdle, Joseph J Witzemann, Veit Producer: 20120607 In: Neurobiology of disease vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	C9ORF72-ALS: P62- and ubiquitin-aggregation pathology in skeletal muscle. [electronic resource] by Türk, Matthias Haaker, Gerrit Winter, Lilli Just, Walter Nickel, Florian T Linker, Ralf A Chevessier, Frédéric Schröder, Rolf Producer: 20141006 In: Muscle & nerve vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Human skeletal muscle triadin: gene organization and cloning of the major isoform, Trisk 51. [electronic resource] by Thevenon, Dominique Smida-Rezgui, Sophia Chevessier, Frédéric Groh, Séverine Henry-Berger, Joëlle Beatriz Romero, Norma Villaz, Michel DeWaard, Michel Marty, Isabelle Producer: 20030620 In: Biochemical and biophysical research communications vol. 303 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	The origin of tubular aggregates in human myopathies. [electronic resource] by Chevessier, Frédéric Bauché-Godard, Stéphanie Leroy, Jean-Paul Koenig, Jeanine Paturneau-Jouas, Marion Eymard, Bruno Hantaï, Daniel Verdière-Sahuqué, Martine Producer: 20051214 In: The Journal of pathology vol. 207 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Severe protein aggregate myopathy in a knockout mouse model points to an essential role of cofilin2 in sarcomeric actin exchange and muscle maintenance. [electronic resource] by Gurniak, Christine B Chevessier, Frédéric Jokwitz, Melanie Jönsson, Friederike Perlas, Emerald Richter, Hendrik Matern, Gabi Boyl, Pietro Pilo Chaponnier, Christine Fürst, Dieter Schröder, Rolf Witke, Walter Producer: 20150511 In: European journal of cell biology vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Advances in the understanding of skeletal muscle weakness in murine models of diseases affecting nerve-evoked muscle activity, motor neurons, synapses and myofibers. [electronic resource] by Ferry, Arnaud Joanne, Pierre Hadj-Said, Wahiba Vignaud, Alban Lilienbaum, Alain Hourdé, Christophe Medja, Fadia Noirez, Philippe Charbonnier, Frederic Chatonnet, Arnaud Chevessier, Frederic Nicole, Sophie Agbulut, Onnik Butler-Browne, Gillian Producer: 20150720 In: Neuromuscular disorders : NMD vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	CASQ1 mutations impair calsequestrin polymerization and cause tubular aggregate myopathy. [electronic resource] by Böhm, Johann Lornage, Xavière Chevessier, Frederic Birck, Catherine Zanotti, Simona Cudia, Paola Bulla, Monica Granger, Florence Bui, Mai Thao Sartori, Maxime Schneider-Gold, Christiane Malfatti, Edoardo Romero, Norma B Mora, Marina Laporte, Jocelyn Producer: 20190624 In: Acta neuropathologica vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Neuromuscular endplate pathology in recessive desminopathies: Lessons from man and mice. [electronic resource] by Durmuş, Hacer Ayhan, Özgecan Çırak, Sebahattin Deymeer, Feza Parman, Yeşim Franke, Andre Eiber, Nane Chevessier, Frederic Schlötzer-Schrehardt, Ursula Clemen, Christoph S Hashemolhosseini, Said Schröder, Rolf Hemmrich-Stanisak, Georg Tolun, Aslıhan Serdaroğlu-Oflazer, Piraye Producer: 20170529 In: Neurology vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue. [electronic resource] by Winter, Lilli Wittig, Ilka Peeva, Viktoriya Eggers, Britta Heidler, Juliana Chevessier, Frederic Kley, Rudolf A Barkovits, Katalin Strecker, Valentina Berwanger, Carolin Herrmann, Harald Marcus, Katrin Kornblum, Cornelia Kunz, Wolfram S Schröder, Rolf Clemen, Christoph S Producer: 20170922 In: Acta neuropathologica vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Treadmill exercise intervention improves gait and postural control in alpha-synuclein mouse models without inducing cerebral autophagy. [electronic resource] by Minakaki, Georgia Canneva, Fabio Chevessier, Frédéric Bode, Frederik Menges, Stefanie Timotius, Ivanna K Kalinichenko, Liubov S Meixner, Holger Müller, Christian P Eskofier, Bjoern M Casadei, Nicolas Riess, Olaf Schröder, Rolf Winkler, Jürgen Xiang, Wei von Hörsten, Stephan Klucken, Jochen Producer: 20190830 In: Behavioural brain research vol. 363 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	[Pathophysiological characterization of congenital myasthenic syndromes: the example of mutations in the MUSK gene]. [electronic resource] by Chevessier, Frédéric Faraut, Brice Ravel-Chapuis, Aymeric Richard, Pascale Gaudon, Karen Bauché, Stéphanie Prioleau, Cassandra Herbst, Ruth Goillot, Evelyne Ioos, Christine Azulay, Jean-Philippe Attarian, Shahram Leroy, Jean-Paul Fournier, Emmanuel Legay, Claire Schaeffer, Laurent Koenig, Jeanine Fardeau, Michel Eymard, Bruno Pouget, Jean Hantaï, Daniel Producer: 20051014 In: Journal de la Societe de biologie vol. 199 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1. [electronic resource] by Böhm, Johann Chevessier, Frédéric Koch, Catherine Peche, G Arielle Mora, Marina Morandi, Lucia Pasanisi, Barbara Moroni, Isabella Tasca, Giorgio Fattori, Fabiana Ricci, Enzo Pénisson-Besnier, Isabelle Nadaj-Pakleza, Aleksandra Fardeau, Michel Joshi, Pushpa Raj Deschauer, Marcus Romero, Norma Beatriz Eymard, Bruno Laporte, Jocelyn Producer: 20150709 In: Journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	VCP and PSMF1: Antagonistic regulators of proteasome activity. [electronic resource] by Clemen, Christoph S Marko, Marija Strucksberg, Karl-Heinz Behrens, Juliane Wittig, Ilka Gärtner, Linda Winter, Lilli Chevessier, Frederic Matthias, Jan Türk, Matthias Tangavelou, Karthikeyan Schütz, Johanna Arhzaouy, Khalid Klopffleisch, Karsten Hanisch, Franz-Georg Rottbauer, Wolfgang Blümcke, Ingmar Just, Steffen Eichinger, Ludwig Hofmann, Andreas Schröder, Rolf Producer: 20151102 In: Biochemical and biophysical research communications vol. 463 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Myofibrillar instability exacerbated by acute exercise in filaminopathy. [electronic resource] by Chevessier, Frédéric Schuld, Julia Orfanos, Zacharias Plank, Anne-C Wolf, Lucie Maerkens, Alexandra Unger, Andreas Schlötzer-Schrehardt, Ursula Kley, Rudolf A Von Hörsten, Stephan Marcus, Katrin Linke, Wolfgang A Vorgerd, Matthias van der Ven, Peter F M Fürst, Dieter O Schröder, Rolf Producer: 20160920 In: Human molecular genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Identification of an agrin mutation that causes congenital myasthenia and affects synapse function. [electronic resource] by Huzé, Caroline Bauché, Stéphanie Richard, Pascale Chevessier, Frédéric Goillot, Evelyne Gaudon, Karen Ben Ammar, Asma Chaboud, Annie Grosjean, Isabelle Lecuyer, Heba-Aude Bernard, Véronique Rouche, Andrée Alexandri, Nektaria Kuntzer, Thierry Fardeau, Michel Fournier, Emmanuel Brancaccio, Andrea Rüegg, Markus A Koenig, Jeanine Eymard, Bruno Schaeffer, Laurent Hantaï, Daniel Producer: 20090923 In: American journal of human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathy. [electronic resource] by Böhm, Johann Chevessier, Frédéric Maues De Paula, André Koch, Catherine Attarian, Shahram Feger, Claire Hantaï, Daniel Laforêt, Pascal Ghorab, Karima Vallat, Jean-Michel Fardeau, Michel Figarella-Branger, Dominique Pouget, Jean Romero, Norma B Koch, Marc Ebel, Claudine Levy, Nicolas Krahn, Martin Eymard, Bruno Bartoli, Marc Laporte, Jocelyn Producer: 20130404 In: American journal of human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 25 results.