Ergebnisse einschränken

Nerve ultrasound for differentiation between amyotrophic lateral sclerosis and multifocal motor neuropathy

Grimm, Alexander ; Décard, Bernhard ; Athanasopoulou, Ioanna ; Schweikert, Kathi ; Sinnreich, Michael ; Axer, Hubertus

In: Journal of Neurology, 2015, vol. 262, no. 4, p. 870-880

Schwann cells ER-associated degradation contributes to myelin maintenance in adult nerves and limits demyelination in CMT1B mice

Volpi, Vera G. ; Ferri, Cinzia ; Fregno, Ilaria ; Del Carro, Ubaldo ; Bianchi, Francesca ; Scapin, Cristina ; Pettinato, Emanuela ; Solda, Tatiana ; Feltri, M. Laura ; Molinari, Maurizio ; Wrabetz, Lawrence ; D’Antonio, Maurizio

In: PLOS genetics, 2019, vol. 15, no. 4, p. e1008069

In the peripheral nervous system (PNS) myelinating Schwann cells synthesize large amounts of myelin protein zero (P0) glycoprotein, an abundant component of peripheral nerve myelin. In humans, mutations in P0 cause the demyelinating Charcot-Marie-Tooth 1B (CMT1B) neuropathy, one of the most diffused genetic disorders of the PNS. We previously showed that several mutations, such as the...

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 expansion of 300 CTG repeats in myotonic dystrophy transgenic mice does not induce sensory or motor neuropathy

Gantelet, E. ; Kraftsik, R. ; Delaloye, S. ; Gourdon, G. ; Kuntzer, T. ; Barakat-Walter, I.

In: Acta Neuropathologica, 2007, vol. 114, no. 2, p. 175-185

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

Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease

Niemann, Axel ; Berger, Philipp ; Suter, Ueli

In: NeuroMolecular Medicine, 2006, vol. 8, no. 1-2, p. 217-241

High resolution neurochemical gold staining method for myelin in peripheral and central nervous system at the light- and electron-microscopic level

Savaskan, Nic ; Weinmann, Oliver ; Heimrich, Bernd ; Eyupoglu, Ilker

In: Cell and Tissue Research, 2009, vol. 337, no. 2, p. 213-221

Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2

Tersar, Kristian ; Boentert, Matthias ; Berger, Philipp ; Bonneick, Sonja ; Wessig, Carsten ; Toyka, Klaus V. ; Young, Peter ; Suter, Ueli

In: Human Molecular Genetics, 2007, vol. 16, no. 24, p. 2991-3001

PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease

Azzedine, Hamid ; Zavadakova, Petra ; Planté-Bordeneuve, Violaine ; Vaz Pato, Maria ; Pinto, Nuno ; Bartesaghi, Luca ; Zenker, Jennifer ; Poirot, Olivier ; Bernard-Marissal, Nathalie ; Arnaud Gouttenoire, Estelle ; Cartoni, Romain ; Title, Alexandra ; Venturini, Giulia ; Médard, Jean-Jacques ; Makowski, Edward ; Schöls, Ludger ; Claeys, Kristl G. ; Stendel, Claudia ; Roos, Andreas ; Weis, Joachim ; Dubourg, Odile ; Leal Loureiro, José ; Stevanin, Giovanni ; Said, Gérard ; Amato, Anthony ; Baraban, Jay ; LeGuern, Eric ; Senderek, Jan ; Rivolta, Carlo ; Chrast, Roman

In: Human Molecular Genetics, 2013, vol. 22, no. 20, p. 4224-4232

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