[1] N. Latronico, and C.F. Bolton, Critical illness polyneuropathy and myopathy: a major cause of muscle weakness and paralysis. The Lancet Neurology 10 (2011) 931-941.
[2] W. Trojaborg, L.H. Weimer, and A.P. Hays, Electrophysiologic studies in critical illness associated weakness: myopathy or neuropathy – a reappraisal. Clinical Neurophysiology 112 (2001) 1586-1593.
[3] M.W. Faragher, B.J. Day, and X. Dennett, Critical care myopathy: An electrophysiological and histological study. Muscle & Nerve 19 (1996) 516-518.
[4] J.P. Kress , and J.B. Hall ICU-Acquired Weakness and Recovery from Critical Illness. New England Journal of Medicine 370 (2014) 1626-1635.
[5] E. Hund, Neurological complications of sepsis: critical illness polyneuropathy and myopathy. Journal of Neurology 248 (2001) 929-934.
[6] A.J. Lewis, C.W. Seymour, and M.R. Rosengart, Current Murine Models of Sepsis. Surg Infect (Larchmt) 17 (2016) 385-393.
[7] T. Dziedzic, Systemic inflammation as a therapeutic target in acute ischemic stroke. Expert review of neurotherapeutics 15 (2015) 523-31.
[8] W.F. Westendorp, P.J. Nederkoorn, J.-D. Vermeij, M.G. Dijkgraaf, and D.v. de Beek, Post-stroke infection: A systematic review and meta-analysis. BMC Neurology 11 (2011) 110-110.
[9] B. Berger, C. Gumbinger, T. Steiner, and M. Sykora, Epidemiologic features, risk factors, and outcome of sepsis in stroke patients treated on a neurologic intensive care unit. Journal of critical care 29 (2014) 241-8.
[10] N. Scherbakov, S. von Haehling, S.D. Anker, U. Dirnagl, and W. Doehner, Stroke induced Sarcopenia: muscle wasting and disability after stroke. International journal of cardiology 170 (2013) 89-94.
[11] M.L. Harris, M.I. Polkey, P.M. Bath, and J. Moxham, Quadriceps muscle weakness following acute hemiplegic stroke. Clin Rehabil 15 (2001) 274-81.
[12] J. Springer, S. Schust, K. Peske, A. Tschirner, A. Rex, O. Engel, N. Scherbakov, A. Meisel, S. von Haehling, M. Boschmann, S.D. Anker, U. Dirnagl, and W. Doehner, Catabolic signaling and muscle wasting after acute ischemic stroke in mice: indication for a stroke-specific sarcopenia. Stroke 45 (2014) 3675-83.
[13] C.E. Hafer-Macko, A.S. Ryan, F.M. Ivey, and R.F. Macko, Skeletal muscle changes after hemiparetic stroke and potential beneficial effects of exercise intervention strategies. J Rehabil Res Dev 45 (2008) 261-272.
[14] J.B. Bederson, L.H. Pitts, M. Tsuji, M.C. Nishimura, R.L. Davis, and H. Bartkowski, Rat middle cerebral artery occlusion: evaluation of the model and development of a neurologic examination. Stroke 17 (1986) 472.
[15] C. Meisel, K. Prass, J. Braun, I. Victorov, T. Wolf, D. Megow, E. Halle, H.D. Volk, U. Dirnagl, and A. Meisel, Preventive antibacterial treatment improves the general medical and neurological outcome in a mouse model of stroke. Stroke 35 (2004) 2-6.
[16] U. Dirnagl, and M.o.t.M.-S. Group, Standard operating procedures (SOP) in experimental stroke research: SOP for middle cerebral artery occlusion in the mouse. Nature Precedings (2012) 1–14.
[17] O. Engel, S. Kolodziej, U. Dirnagl, and V. Prinz, Modeling Stroke in Mice - Middle Cerebral Artery Occlusion with the Filament Model. Journal of Visualized Experiments : JoVE (2011) 2423.
[18] F. Krieger, N. Elflein, S. Saenger, E. Wirthgen, K. Rak, S. Frantz, A. Hoeflich, K.V. Toyka, F. Metzger, and S. Jablonka, Polyethylene glycol-coupled IGF1 delays motor function defects in a mouse model of spinal muscular atrophy with respiratory distress type 1. Brain 137 (2014) 1374-93.
[19] P. Huehnchen, and W. Boehmerle, Focal brain ischemia in mice does not cause electrophysiological signs of critical illness neuropathy. Mendeley Data V1 (2020).
[20] S.T. Carmichael, Rodent Models of Focal Stroke: Size, Mechanism, and Purpose. NeuroRx 2 (2005) 396-409.
[21] S.-Y. Park, S. Marasini, G.-H. Kim, T. Ku, C. Choi, M.-Y. Park, E.-H. Kim, Y.-D. Lee, H. Suh-Kim, and S.-S. Kim, A Method for Generate a Mouse Model of Stroke: Evaluation of Parameters for Blood Flow, Behavior, and Survival. Experimental Neurobiology 23 (2014) 104-114.
[22] P. Huehnchen, W. Boehmerle, and M. Endres, High salt diet ameliorates functional, electrophysiological and histological characteristics of murine spontaneous autoimmune polyneuropathy. Neurobiology of disease 124 (2019) 240-247.
[23] P. Huehnchen, W. Boehmerle, and M. Endres, Fingolimod therapy is not effective in a mouse model of spontaneous autoimmune peripheral polyneuropathy. Sci Rep 8 (2018) 5648.
[24] L. Wrabetz, M. D'Antonio, M. Pennuto, G. Dati, E. Tinelli, P. Fratta, S. Previtali, D. Imperiale, J. Zielasek, K. Toyka, R.L. Avila, D.A. Kirschner, A. Messing, M.L. Feltri, and A. Quattrini, Different intracellular pathomechanisms produce diverse Myelin Protein Zero neuropathies in transgenic mice. The Journal of neuroscience : the official journal of the Society for Neuroscience 26 (2006) 2358-68.
[25] L. Li, Y. Li, Z. Fan, X. Wang, Z. Li, J. Wen, J. Deng, D. Tan, M. Pan, X. Hu, H. Zhang, M. Lai, and J. Guo, Ascorbic Acid Facilitates Neural Regeneration After Sciatic Nerve Crush Injury. Frontiers in Cellular Neuroscience 13 (2019).
[26] A. Murat Kalender, A. Dogan, V. Bakan, H. Yildiz, M. Ata Gokalp, and M. Kalender, Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model. Journal of Brachial Plexus and Peripheral Nerve Injury 4 (2009) 6.
[27] C.F. Bolton, Electrophysiologic studies of critically ill patients. Muscle & Nerve 10 (1987) 129-135.
[28] B. Tabarki, A. Coffiniéres, P. Van den Bergh, G. Huault, P. Landrieu, and G. Sébire, Critical illness neuromuscular disease: clinical, electrophysiological, and prognostic aspects. Archives of Disease in Childhood 86 (2002) 103-107.
[29] A.B. Caglayan, M.C. Beker, B. Caglayan, E. Yalcin, A. Caglayan, B. Yulug, L. Hanoglu, S. Kutlu, T.R. Doeppner, D.M. Hermann, and E. Kilic, Acute and Post-acute Neuromodulation Induces Stroke Recovery by Promoting Survival Signaling, Neurogenesis, and Pyramidal Tract Plasticity. Frontiers in Cellular Neuroscience 13 (2019).
[30] B. Manwani, F. Liu, Y. Xu, R. Persky, J. Li, and L.D. McCullough, Functional recovery in aging mice after experimental stroke. Brain, behavior, and immunity 25 (2011) 1689-1700.
[31] H. Kassem-Moussa, and C. Graffagnino, Nonocclusion and Spontaneous Recanalization Rates in Acute Ischemic Stroke: A Review of Cerebral Angiography Studies. Archives of Neurology 59 (2002) 1870-1873.