Stereotactic surgery of nucleus tegmenti pedunculopontini

References

• Anderson W S, Lenz F A. Surgery insight: Deep brain stimulation for movement disorders. Nat Clin Pract Neuro 2006; 2: 310–320
   PubMedGoogle Scholar
• Benabid A L. What the future holds for deep brain stimulation. Expert Rev Med Devices 2007; 4: 895–903
   PubMed Web of Science ®Google Scholar
• Benabid A L, Chabardès S, Seigneuret E. Deep-brain stimulation in Parkinson's disease: long-term efficacy and safety – What happened this year?. Curr Opin Neurol 2005; 18: 623–630
   PubMed Web of Science ®Google Scholar
• Kleiner-Fisman G, Herzog J, Fisman D N, Tamma F, Lyons K E, Pahwa R, Lang A E, Deuschl G. Subthalamic nucleus deep brain stimulation: summary and metaanalysis of outcomes. Mov Disord 2006; 21(Suppl 14)S290–S304
   PubMed Web of Science ®Google Scholar
• Pahwa R, Factor S A, Lyons K E, Ondo W G, Gronseth G, Bronte-Stewart H, Hallet M, Miyasaki J, Stevens J, et al. Quality Standards Subcommittee of the American Academy of Neurology. Practice Parameter: treatment of Parkinson disease with motor fluctuations and dyskinesia (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology 2006; 66: 983–995
   PubMed Web of Science ®Google Scholar
• Mazzone P, Stanzione P, Stefani A, Bassi A, Gattoni G, Altibrandi M G. Contemporary bilateral targeting of GPi and STN by Maranello stereotactic system for deep brain stimulation. Proceedings of 11th European Congress of Neurosurgery (EANS), P D Monduzzi. Bologna, Italy 1999; 729–734
   Google Scholar
• Mazzone P. Deep brain stimulation in Parkinson's disease: bilateral implantation of globus pallidus and subthalamic nucleus. J Neurosurg Sci 2003; 47: 47–51
   PubMedGoogle Scholar
• Mazzone P, Brown P, Di Lazzaro V, Stanzione P, Oliviero A, Peppe A, Santilli V, Insola A, Altibrandi M. Bilateral implantation in globus pallidus internus and in subthalamic nucleus in Parkinson's disease. Neuromodulation 2005; 8: 1–6
   PubMedGoogle Scholar
• Mazzone P, Insola A, Brown P, Di Lazzaro V, Tonali P, Altibrandi M G. Contemporary bilateral DBS on GPi and STN nuclei and preliminary results on contemporary bilateral DBS on GPi and CM-Pf complex in PD. Abstracts of the 16th Congress of the European Society for Stereotactic and Functional Neurosurgery (ESSFN), Vienna, Austria, June 23–26, 2004. Acta Neurochir (Wien), 146: 883, (Abstract 3A12)
   Google Scholar
• Peppe A, Pierantozzi M, Bassi A, Altibrandi M G, Brusa L, Stefani A, Stanzione P, Mazzone P. Stimulation of the subthalamic nucleus compared with the globus pallidus internus in patients with Parkinson disease. J Neurosurg 2004; 101: 195–200
   PubMed Web of Science ®Google Scholar
• Rodriguez-Oroz M C, Obeso J A, Lang A E, Houeto J L, Pollak P, Rehncrona S, et al. Bilateral deep brain stimulation in Parkinson's disease: a multicentre study with 4 years follow-up. Brain 2005; 128: 2240–2249
   PubMed Web of Science ®Google Scholar
• Kumar R, Lozano A M, Montgomery E, Lang A E. Pallidotomy and deep brain stimulation of the pallidum and subthalamic nucleus in advanced Parkinson's disease. Mov Disord 1998; 13: 73–82
   PubMedGoogle Scholar
• Mazzone P, Stanzione P, Lozano A, Sposato S, Scarnati E, Stefani A. Deep Brain Stimulation and movement disorders: where are we going?. Proceedings of 14th Meeting of the World Society of Stereotactic and Functional Neurosurgery (WSSFN), Meglio M. Monduzzi Bologna, Italy 2005
   Google Scholar
• Matsumura M, Kojima J. The role of the pedunculopontine tegmental nucleus in experimental parkinsonism in primates. Stereotact Funct Neurosurg 2001; 77: 108–115
   PubMedGoogle Scholar
• Takakusaki K, Saitoh K, Harada H, Okumura T, Sakamoto T. Evidence for a role of basal ganglia in the regulation of rapid eye movement sleep by electrical and chemical stimulation for the pedunculopontine tegmental nucleus and the substantia nigra pars reticulata in decerebrate cats. Neuroscience 2004; 124: 207–220
   PubMedGoogle Scholar
• Scarnati E, Florio T. The pedunculopontine nucleus and related structures. Functional organization. Adv Neurol 1997; 74: 97–110
   PubMedGoogle Scholar
• Florio T, Scarnati E, Confalone G, Minchella D, Galati S, Stanzione P, Stefani A, Mazzone P. High-frequency stimulation of the subthalamic nucleus modulates the activity of pedunculopontine neurons through direct activation of excitatory fibres as well as through indirect activation of inhibitory pallidal fibres in he rat. Eur J Neurosci 2007; 25: 1174–1186
   PubMedGoogle Scholar
• Jenkinson N, Nandi D, Oram R, Stein J F, Aziz T Z. Pedunculopontine nucleus electric stimulation alleviates akinesia independently of dopaminergic mechanisms. Neuroreport 2006; 17: 639–641
   PubMed Web of Science ®Google Scholar
• Mena-Segovia J, Ross H M, Magill P J, Bolam J. P. The Pedunculopontine Nucleus: Towards a Functional Integration with the Basal Ganglia. The Basal Ganglia VIII, J P Bolam, C A Ingham, P J Magill. Springer Science and Business Media, New York 2005; 533–544
   Google Scholar
• Mena-Segovia J, Bolam J P, Magill P J. Pedunculopontine nucleus and basal ganglia: distant relatives or part of the same family?. Trends Neurosci 2004; 27: 585–588
   PubMed Web of Science ®Google Scholar
• Pahapill P A, Lozano A M. The pedunculopontine nucleus and Parkinson's disease. Brain 2000; 123: 1767–1783
   PubMed Web of Science ®Google Scholar
• Aravamuthan B R, Muthusamy K A, Stein J F, Aziz T Z, Johansen-Berg H. Topography of cortical and subcortical connections of the human pedunculopontine and subthalamic nuclei. Neuroimage 2007; 37: 694–705
   PubMed Web of Science ®Google Scholar
• Breit S, Lessmann L, Unterbrink D, Popa R C, Gasser T, Schulz J B. Lesion of the pedunculopontine nucleus reverses hyperactivity of the subthalamic nucleus and substantia nigra pars reticulata in a 6-hydroxydopamine rat model. Eur J Neurosci 2006; 24: 2275–2282
   PubMedGoogle Scholar
• Stefani A, Lozano A M, Peppe A, Stanzione P, Galati S, Tropepi D, et al. Bilateral deep brain stimulation of the pedunculopontine and subthalamic nuclei in severe Parkinson's disease. Brain 2007; 130: 1596–1607
   PubMed Web of Science ®Google Scholar
• Mazzone P, Lozano A, Stanzione P, Galati S, Scarnati E, Peppe A, Stefani A. Implantation of human pedunculopontine nucleus: a safe and clinically relevant target in Parkinson's disease. Neuroreport 2005; 16: 1877–1881
   PubMed Web of Science ®Google Scholar
• Plaha P, Gill S S. Bilateral ddep brain stimulation of the pedunculopontine nucleus for Parkinson's disease. Neuroreport 2005; 16: 1883–1887
   PubMed Web of Science ®Google Scholar
• Mazzone P. Il sistema stereotassico 3P Maranello. Europa Medicophisica 2001; 3: 318–319
   Google Scholar
• Mazzone P. The arch-less skull applied stereotactic device. Acta Neurochirurgica 2006; 148: LVIII, (Abstract)
   Google Scholar
• Schaltenbrand G, Wahren W. Atlas for Stereotaxy of the Human Brain. Thieme, Stuttgart, New York 1977
   Google Scholar
• Mazzone P, Stocchi F, Galati S, Insola A, Altibrandi M G, Modugno N. Bilateral implantation of centromedian-parafascicularis complex and GPi: A new combination of unconventional targets for deep brain stimulation in severe Parkinson disease. Neuromodulation 2006; 9: 221–228
   PubMed Web of Science ®Google Scholar
• Mazzone P, Della Marca G, Sposato S, Di Lazzaro V, Scarnati E. Tridimensional modelling of midbrain and pontine structures: a proposed approach to the stereotactic targeting of Pedunculopontine Tegmental Nucleus. Neurotarget 2008, (in press)
   Google Scholar
• Olszewski J, Baxter D. Cytoarchitecture of the human brain stem. S. Karger, Basel 1982
   Google Scholar
• Paxinos G, Huang X F. Atlas of the Human Brainstem. Academic Press, San Diego 1995
   Google Scholar
• Afshar E, Watkins E S, Yap J C. Stereotactic Atlas of the Human Brainstem and Cerebellar Nuclei. Raven Press, New York 1978
   Google Scholar
• Niemann K, van den Boom R, Haeselbarth K, Afshar F. A brainstem stereotactic atlas in a three-dimensional magnetic resonance imaging navigation system: first experiences with atlas-to-patient registration. J Neurosurg 1999; 90: 891–901
   PubMedGoogle Scholar
• Lang A E, Houeto J L, Krack P, Kubu C, Lyons K E, Moro E, Ondo W, Pahwa R, Poewe W, Troster A I, et al. Deep brain stimulation: preoperative issues. Mov Disord 2006; 21: S171–S196
   PubMed Web of Science ®Google Scholar
• Young R F, Tronnier V, Rinaldi P C. Chronic stimulation of the Kölliker-Fuse nucleus region for relief of intractable pain in humans. J Neurosurg 1992; 76: 979–985
   PubMedGoogle Scholar
• Talairach J, David M, Tournoux P, Corredor H, Kvasina T. Atlas d'anatomie stéréotaxique des noyaux gris centraux. Masson, Paris 1957
   Google Scholar
• Talairach J, Tournoux P. Co-Planar Stereotaxic Atlas of the Human Brain: 3-Dimensional Proportional System. An Approach to Cerebral Imaging. Thieme, Stuttgart 1988
   Google Scholar
• Muthusamy K A, Aravamuthan B R, Kringelbach M L, Jenkinson N, Voets N L, Johansen-Berg H, Stein J F, Aziz T Z. Connectivity of the human pedunculopontine nucleus region and diffusion tensor imaging in surgical targeting. J Neurosurg 2007; 107: 814–820
   PubMed Web of Science ®Google Scholar
• Benabid A L, Benazzouz A, Hoffmann D, Limousin P, Krack P, Pollak P. Long-term electrical inhibition of deep brain targets in movement disorders. Mov Disord 1998; 13: 119–125
   PubMed Web of Science ®Google Scholar
• Nowinski W L, Belov D, Thirunavuukarasuu A, Benabid A L. A probabilistic functional atlas of the VIM nucleus constructed from pre-, intra- and postoperative electrophysiological and neuroimaging data acquired during the surgical treatment of Parkinson's disease patients. Stereotact Funct Neurosurg 2005; 83: 190–196
   PubMedGoogle Scholar
• Li J, Andrews R J. Trimodal nanoelectrode array for precise deep brain stimulation: prospects of a new technology based on carbon nanofiber arrays. Acta Neurochir Suppl 2007; 97: 537–545
   PubMedGoogle Scholar