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Neurobiology of Disease|November 11, 2008
The co-inhibitory molecule PD-1 modulates disease severity in a model for an inherited, demyelinating neuropathyAntje Kroner, Nicholas Schwab, Chi Wang Ip, et al.
Lancet (London, England)|April 20, 2005
Paraneoplastic stiff-person syndrome: passive transfer to rats by means of IgG antibodies to amphiphysinClaudia Sommer, Andreas Weishaupt, Jörg Brinkhoff, et al.
Fertility and Sterility|February 13, 2010
Magnetic resonance neurography for the diagnosis of extrapelvic sciatic endometriosisMirko Pham, Claudia Sommer, Carsten Wessig, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 10, 2003
The Wlds mutation delays robust loss of motor and sensory axons in a genetic model for myelin-related axonopathyMohtashem Samsam, Weiqian Mi, Carsten Wessig, et al.
Journal of Medical Case Reports|January 12, 2013
Fatal atypical reversible posterior leukoencephalopathy syndrome: a case reportStefanie Kristin Golombeck, Carsten Wessig, Camelia-Maria Monoranu, et al.
Case Reports in Anesthesiology|September 14, 2012
In vitro contracture test results and anaesthetic management of a patient with emery-dreifuss muscular dystrophy for cardiac transplantationFrank Schuster, Carsten Wessig, Christoph Schimmer, et al.
Annals of Neurology|February 26, 2005
Assessment of nerve degeneration by gadofluorine M-enhanced magnetic resonance imagingMartin Bendszus, Carsten Wessig, Ansgar Schütz, et al.
Human Molecular Genetics|September 15, 2007
Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2Kristian Tersar, Matthias Boentert, Philipp Berger, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|October 30, 2008
Transient widespread blood-brain barrier alterations after cerebral photothrombosis as revealed by gadofluorine M-enhanced magnetic resonance imagingGuido Stoll, Christoph Kleinschnitz, Sven G Meuth, et al.
The Journal of Cell Biology|May 19, 2004
Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorderAnnette E Rünker, Igor Kobsar, Torsten Fink, et al.
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