Outcomes from stimulation of the caudal zona incerta and pedunculopontine nucleus in patients with Parkinson's disease

References

• Schrag A, Jahanshahi M, Quinn N. What contributes to quality of life in patients with Parkinson's disease? J Neurol Neurosurg Psychiatry 2000;69:308–12.
   PubMed Web of Science ®Google Scholar
• Bonnet AM, Loria Y, Saint-Hilaire MH, Lhermitte F, Agid Y. Does long-term aggravation of Parkinson's disease result from nondopaminergic lesions? Neurology 1987;37:1539–42.
   PubMed Web of Science ®Google Scholar
• Deuschl G, Schade-Brittinger C, Krack P, et al. A randomized trial of deep-brain stimulation for Parkinson's disease. N Engl J Med 2006;355:896–908.
   PubMed Web of Science ®Google Scholar
• Guehl D, Cuny E, Benazzouz A, et al. Side-effects of subthalamic stimulation in Parkinson's disease: clinical evolution and predictive factors. Eur J Neurol 2006;13:963–71.
   PubMed Web of Science ®Google Scholar
• Plaha P, Gill SS. Bilateral deep brain stimulation of the pedunculopontine nucleus for Parkinson's disease. Neuroreport 2005;16:1883–7.
   PubMed Web of Science ®Google Scholar
• Stefani A, Lozano AM, Peppe A, et al. Bilateral deep brain stimulation of the pedunculopontine and subthalamic nuclei in severe Parkinson's disease. Brain 2007;130:1596–607.
   PubMed Web of Science ®Google Scholar
• Mazzone P, Lozano A, Stanzione P, et al. Implantation of human pedunculopontine nucleus: a safe and clinically relevant target in Parkinson's disease. Neuroreport 2005;16:1877–81.
   PubMed Web of Science ®Google Scholar
• Moro E, Hamani C, Poon YY, et al. Unilateral pedunculopontine stimulation improves falls in Parkinson's disease. Brain 2010;133:215–24.
   PubMed Web of Science ®Google Scholar
• Ferraye MU, Debu B, Fraix V, et al. Effects of pedunculopontine nucleus area stimulation on gait disorders in Parkinson's disease. Brain 2008;79:514–21.
   Google Scholar
• Plaha P, Ben-Shlomo Y, Patel NK, Gill SS. Stimulation of the caudal zona incerta is superior to stimulation of the subthalamic nucleus in improving contralateral parkinsonism. Brain 2006;129:1732–47.
   PubMed Web of Science ®Google Scholar
• Nieuwenhuys R, Voogd J, van Huijzen C. The human central nervous system.4th edBerlin: Springer, 2008.
   Google Scholar
• Paxinos G, Huang X. Atlas of the human brainstemSan Diego: Academic Press, 1995.
   Google Scholar
• Khan S, Javed S, Patel NK, Plaha P, Gill S. Pedunculopontine DBS in advanced Parkinson's disease. Deep brain stimulation. In: Bain P, Aziz T, Liu X, Nandi D, eds. 1st edOxford: Oxford University Press, 2009: 27–34.
   Google Scholar
• Khan S, Javed S, Park N, Gill SS, Patel NK. A magnetic resonance imaging-directed method for transventricular targeting of midline structures for deep brain stimulation using implantable guide tubes. Neurosurgery 2010;66:234–7; discussion 37.
   PubMed Web of Science ®Google Scholar
• Patel NK, Plaha P, Gill SS. Magnetic resonance imaging-directed method for functional neurosurgery using implantable guide tubes. Neurosurgery 2007;61:358–65; discussion 65–6.
   PubMed Web of Science ®Google Scholar
• Zrinzo L, Zrinzo LV, Tisch S, et al. Stereotactic localization of the human pedunculopontine nucleus: atlas-based coordinates and validation of a magnetic resonance imaging protocol for direct localization. Brain 2008;131:1588–98.
   PubMed Web of Science ®Google Scholar
• Mazzone P, Sposato S, Insola A, Dilazzaro V, Scarnati E. Stereotactic surgery of nucleus tegmenti pedunculopontine [corrected]. Br J Neurosurg 2008;22(Suppl 1):S33–40.
   Google Scholar
• Langston JW, Widner H, Goetz CG, et al. Core assessment program for intracerebral transplantations (CAPIT). Mov Disord 1992;7:2–13.
   PubMed Web of Science ®Google Scholar
• Ferraye MU, Gerardin P, Debu B, et al. Pedunculopontine nucleus stimulation induces monocular oscillopsia. J Neurol Neurosurg Psychiatry 2009;80:228–31.
   PubMed Web of Science ®Google Scholar
• Monge A, Viselli F, Stocchi F, et al. Variation in the dopaminergic response during the day in Parkinson disease. Clin Neuropharmacol 2004;27:116–8.
   PubMed Web of Science ®Google Scholar
• Wright WG, Gurfinkel VS, Nutt J, Horak FB, Cordo PJ. Axial hypertonicity in Parkinson's disease: direct measurements of trunk and hip torque. Exp Neurol 2007;208:38–46.
   PubMed Web of Science ®Google Scholar
• Tinetti ME. Performance-oriented assessment of mobility problems in elderly patients. J Am Geriatr Soc 1986;34:119–26.
   PubMed Web of Science ®Google Scholar
• Moreau C, Defebvre L, Destee A, et al. STN-DBS frequency effects on freezing of gait in advanced Parkinson disease. Neurology 2008;71:80–4.
   PubMed Web of Science ®Google Scholar
• Bruno RM, Sakmann B. Cortex is driven by weak but synchronously active thalamocortical synapses. Science 2006;312:1622–7.
   PubMed Web of Science ®Google Scholar
• Schoffelen JM, Oostenveld R, Fries P. Neuronal coherence as a mechanism of effective corticospinal interaction. Science 2005;308:111–3.
   PubMed Web of Science ®Google Scholar
• Brown P, Marsden CD. What do the basal ganglia do? Lancet 1998;351:1801–4.
   PubMed Web of Science ®Google Scholar
• Gilbertson T, Lalo E, Doyle L, et al. Existing motor state is favored at the expense of new movement during 13–35 Hz oscillatory synchrony in the human corticospinal system. J Neurosci 2005;25:7771–9.
   PubMed Web of Science ®Google Scholar
• Cassidy M, Mazzone P, Oliviero A, et al. Movement-related changes in synchronization in the human basal ganglia. Brain 2002;125:1235–46.
   PubMed Web of Science ®Google Scholar
• Williams D, Tijssen M, Van Bruggen G, et al. Dopamine-dependent changes in the functional connectivity between basal ganglia and cerebral cortex in humans. Brain 2002;125:1558–69.
   PubMed Web of Science ®Google Scholar
• Womelsdorf T, Schoffelen JM, Oostenveld R, et al. Modulation of neuronal interactions through neuronal synchronization. Science 2007;316:1609–12.
   PubMed Web of Science ®Google Scholar
• Plaha P, Filipovic S, Gill SS. Induction of parkinsonian resting tremor by stimulation of the caudal zona incerta nucleus: a clinical study. J Neurol Neurosurg Psychiatry 2007;133: 205–14.
   Google Scholar
• Brown P, Williams D. Basal ganglia local field potential activity: character and functional significance in the human. Clin Neurophysiol 2005;116:2510–9.
   PubMed Web of Science ®Google Scholar
• Hammond C, Bergman H, Brown P. Pathological synchronization in Parkinson's disease: networks, models and treatments. Trends Neurosci 2007;30:357–64.
   PubMed Web of Science ®Google Scholar
• Allert N, Volkmann J, Dotse S, et al. Effects of bilateral pallidal or subthalamic stimulation on gait in advanced Parkinson's disease. Mov Disord 2001;16:1076–85.
   PubMed Web of Science ®Google Scholar
• Rodriguez-Oroz MC, Obeso JA, Lang AE, et al. Bilateral deep brain stimulation in Parkinson's disease: a multicentre study with 4 years follow-up. Brain 2005;128:2240–9.
   PubMed Web of Science ®Google Scholar
• Bohnen NI, Muller ML, Koeppe RA, et al. History of falls in Parkinson disease is associated with reduced cholinergic activity. Neurology 2009;73:1670–6.
   PubMed Web of Science ®Google Scholar
• Jellinger K. The pedunculopontine nucleus in Parkinson's disease, progressive supranuclear palsy and Alzheimer's disease. J Neurol Neurosurg Psychiatry 1988;51:540–3.
   PubMed Web of Science ®Google Scholar
• Asahina M, Suhara T, Shinotoh H, et al. Brain muscarinic receptors in progressive supranuclear palsy and Parkinson's disease: a positron emission tomographic study. J Neurol Neurosurg Psychiatry 1998;65:155–63.
   PubMed Web of Science ®Google Scholar
• Hausdorff JM, Doniger GM, Springer S, et al. A common cognitive profile in elderly fallers and in patients with Parkinson's disease: the prominence of impaired executive function and attention. Exp Aging Res 2006;32:411–29.
   PubMed Web of Science ®Google Scholar
• Garcia-Rill E, Skinner RD, Miyazato H, Homma Y. Pedunculopontine stimulation induces prolonged activation of pontine reticular neurons. Neuroscience 2001;104:455–65.
   PubMed Web of Science ®Google Scholar