Affiner les résultats

Phosphoinositides and Charcot-Marie-Tooth disease: New keys to old questions

Suter, U.

In: Cellular and Molecular Life Sciences, 2007, vol. 64, no. 24, p. 3261-3265

The causes of Charcot-Marie-Tooth disease

Young, P. ; Suter, U.

In: Cellular and Molecular Life Sciences CMLS, 2003, vol. 60, no. 12, p. 2547-2560

Distal axonopathy in peripheral nerves of PMP22-mutant mice

Sancho, Sara ; Magyar, Josef P. ; Aguzzi, Adriano ; Suter1, Ueli

In: Brain, 1999, vol. 122, no. 8, p. 1563-1577

Dynamin 2 mutations in Charcot-Marie-Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination

Sidiropoulos, Páris N. M. ; Miehe, Michaela ; Bock, Thomas ; Tinelli, Elisa ; Oertli, Carole I. ; Kuner, Rohini ; Meijer, Dies ; Wollscheid, Bernd ; Niemann, Axel ; Suter, Ueli

In: Brain, 2012, vol. 135, no. 5, p. 1395-1411

The Gdap1 knockout mouse mechanistically links redox control to Charcot-Marie-Tooth disease

Niemann, Axel ; Huber, Nina ; Wagner, Konstanze M. ; Somandin, Christian ; Horn, Michael ; Lebrun-Julien, Frédéric ; Angst, Brigitte ; Pereira, Jorge A. ; Halfter, Hartmut ; Welzl, Hans ; Feltri, M. Laura ; Wrabetz, Lawrence ; Young, Peter ; Wessig, Carsten ; Toyka, Klaus V. ; Suter, Ueli

In: Brain, 2014, vol. 137, no. 3, p. 668-682

Myelin is dependent on the Charcot-Marie-Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cells

Horn, Michael ; Baumann, Reto ; Pereira, Jorge A. ; Sidiropoulos, Páris N. M. ; Somandin, Christian ; Welzl, Hans ; Stendel, Claudia ; Lühmann, Tessa ; Wessig, Carsten ; Toyka, Klaus V. ; Relvas, João B. ; Senderek, Jan ; Suter, Ueli

In: Brain, 2012, vol. 135, no. 12, p. 3567-3583

Motor axonal sprouting and neuromuscular junction loss in an animal model of Charcot-Marie-Tooth disease

Ang, Eng-Tat ; Schafer, Ralf ; Baltensperger, Richard ; Wernig, Anton ; Celio, Marco ; Sancho Oliver, Sara

In: Journal of Neuropathology & Experimental Neurology, 2010, vol. 69, no. 3, p. 281-293

Muscle weakness in Charcot-Marie-Tooth Type 1A disease (CMT1A) caused by mutations in peripheral myelin protein 22 (PMP22) has been attributed to an axonopathy that results in denervation and muscle atrophy. The underlying pathophysiological mechanisms involved are not understood. We investigated motor performance, neuromuscular junctions (NMJs), physiological parameters, and muscle morphometry...