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1. Full Text Organization of cholinergic, catecholaminergic, serotonergic and orexinergic nuclei in three strepsirrhine primates: Galago demidoff, Perodicticus potto and Lemur catta
by Calvey, Tanya and Patzke, Nina and Kaswera-Kyamakya, Consolate and Gilissen, Emmanuel and Bertelsen, Mads F and Pettigrew, John D and Manger, Paul R
Journal of chemical neuroanatomy, ISSN 0891-0618, 12/2015, Volume 70, pp. 42 - 57
Serotonin | Neural systems | Mammalian evolution | Choline acetyltransferase | Tyrosine hydroxylase | Orexin | Chiroptera | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Lemur - anatomy & histology | Tyrosine 3-Monooxygenase - metabolism | Brain - anatomy & histology | Galago - anatomy & histology | Orexins - metabolism | Species Specificity | Cranial Nerves - metabolism | Galago - metabolism | Choline O-Acetyltransferase - metabolism | Brain - metabolism | Animals | Locus Coeruleus - cytology | Lemur - metabolism | Lorisidae - metabolism | Serotonin - metabolism | Lorisidae - anatomy & histology | Neurons - metabolism | Locus Coeruleus - metabolism | Lemurs | Zoos | Phylogeny | Tyrosine | Bats | Analysis | Monkeys | Hydroxylases | Index Medicus | DRif, dorsal raphe, interfascicular division | DRv, dorsal raphe, ventral division | Hyp.l, lateral hypothalamic cholinergic nucleus | N.Amb, nucleus ambiguus | io, inferior olivary nuclear complex | DRd, dorsal raphe, dorsal division | VI, abducens nucleus | dfu, dorsal funiculus | IP, interpeduncular nucleus | A9v, substantia nigra, ventral, pars reticulata | RtTg, reticulotegmental nucleus of the pons | Hbm, medial habenular nucleus | R, thalamic reticular nucleus | Is.Call | OB, olfactory bulb | Amyg, amygdaloid body | Hyp, hypothalamus | icp, inferior cerebellar peduncle | A16, catecholaminergic neurons of the olfactory bulb | LV, lateral ventricle | A10d, ventral tegmental area, dorsal | pVII, preganglionic motor neurons of the superior salivatory nucleus or facial nerve | scp, superior cerebellar peduncle | VIId, dorsal division of facial nerve nucleus | CLi, caudal linear nucleus | A9l, substantia nigra, lateral | A6c, compact portion of locus coeruleus | PC, cerebral peduncle | PIR, piriform cortex | IV, trochlear nucleus | A7sc, nucleus subcoeruleus, compact portion | C1, rostral ventrolateral medullary tegmental group | A13, zona incerta cell group | DRp, dorsal raphe, peripheral division | DRc, dorsal raphe, caudal division | PPT, pedunculopontine tegmental nucleus | P, putamen nucleus | AP, area postrema | VPO, ventral pontine nucleus | C2, rostral dorsomedial medullary nucleus | EW, Edinger-Westphal nucleus | lot, lateral olfactory tract | Cb, cerebellum | Zic, zona incerta cluster of orexinergic neurons | Rmc, red nucleus, magnocellular division | C, caudate nucleus | DRl, dorsal raphe, lateral division | ac, anterior commissure | X, dorsal motor vagus nucleus | A12, tuberal cell group | xscp, decussation of the superior cerebellar peduncle, zizona incerta | cc, corpus callosum | A10, ventral tegmental area | DCN, deep cerebellar nuclei | vh, ventral horn of spinal cord | N.Bas, nucleus basalis | Hyp.v, ventral hypothalamic cholinergic nucleus | PBg, parabigeminal nucleus | 5n, trigeminal nerve | A8, retrorubral nucleus | NEO, neocortex | CVL, caudal ventrolateral serotonergic group | AON, anterior olfactory nucleus | f, fornix | olfactory tubercle | RPa, raphe pallidus nucleus | Stn, subthalamic nucleus | A2, caudal dorsomedial medullary nucleus | A1, caudal ventrolateral medullary tegmental nucleus | GP, globus pallidus | A9m, substantia nigra, medial | mlf, medial longitudinal fasciculus | LDT, laterodorsal tegmental nucleus | III, oculomotor nucleus | 3V, third ventricle | A10c, ventral tegmental area, central | fr, fasciculus retroflexus | pg, pineal gland | Sep.m, medial septal nucleus | Vmot, motor division of trigeminal nerve nucleus | CO, cochlear nuclear complex | IC, inferior colliculus | lfp, longitudinal fasciculus of the pons | Hbl, lateral habenular nucleus | Hyp.d, dorsal hypothalamic cholinergic nucleus | A15v, anterior hypothalamic group, ventral division | 4V, fourth ventricle | mcp, middle cerebellar peduncle | Cl, claustrum | TOL, islands of Calleja | Mc, main cluster of orexinergic neurons | Hip, hippocampus | ca, cerebral aqueduct | pIX, preganglionic motor neurons of the inferior salivatory nucleus | VIIv, ventral division of facial nerve nucleus | ON, optic nerve | A9pc, substantia nigra, pars compacta | MnR, median raphe nucleus | Sp5, spinal trigeminal tract | S, septal nuclear complex | A4, dorsolateral division of locus coeruleus | GC, central gray matter | OT, optic tract | Vsens, sensory division of trigeminal nerve nucleus | DT, dorsal thalamus | Diag.B, diagonal band of Broca | py, pyramidal tract | RVL, rostral ventrolateral serotonergic group | ROb, raphe obscurus nucleus | A14, rostral periventricular nucleus | ic, internal capsule | A5, fifth arcuate nucleus | B9, supralemniscal serotonergic nucleus | SC, superior colliculus | A11, caudal diencephalic group | N.Acc, nucleus accumbens | pyx, decussation of the pyramidal tract | vfu, ventral funiculus | Otc, optic tract cluster of orexinergic neurons | A6d, diffuse portion of locus coeruleus | A7d, nucleus subcoeruleus, diffuse portion | LGn, lateral geniculate nucleus | XII, hypoglossal nucleus | A10dc, ventral tegmental area, dorsal caudal | A15d, anterior hypothalamic group, dorsal division | RMg, raphe magnus nucleus
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2. Full Text Subthalamic nucleus phase-amplitude coupling correlates with motor impairment in Parkinson’s disease
by van Wijk, Bernadette C.M and Beudel, Martijn and Jha, Ashwani and Oswal, Ashwini and Foltynie, Tom and Hariz, Marwan I and Limousin, Patricia and Zrinzo, Ludvic and Aziz, Tipu Z and Green, Alexander L and Brown, Peter and Litvak, Vladimir
Clinical neurophysiology, ISSN 1388-2457, 2016, Volume 127, Issue 4, pp. 2010 - 2019
Neurology | Cross-frequency coupling | Subthalamic nucleus | Beta oscillations | Local field potentials | Parkinson’s disease | Motor system | Parkinson's disease | HIGH-FREQUENCY OSCILLATIONS | BASAL GANGLIA | FUNCTIONAL CONNECTIVITY | GLOBUS-PALLIDUS | FOLLOW-UP | PATHOLOGICAL SYNCHRONIZATION | CORTEX | DEEP-BRAIN-STIMULATION | MOVEMENT-RELATED CHANGES | BETA-ACTIVITY | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Subthalamic Nucleus - physiopathology | Humans | Beta Rhythm - physiology | Magnetoencephalography - methods | Parkinson Disease - diagnosis | Female | Male | Motor Cortex - physiopathology | Parkinson Disease - physiopathology | Cohort Studies | Deep Brain Stimulation - methods | Medicine, Experimental | Medical research | Index Medicus | DBS, deep brain stimulation | MEG, magnetoencephalography | PAC, phase–amplitude coupling | STN, subthalamic nucleus | UPDRS, Unified Parkinson’s Disease Rating Scale | HFO, high-frequency oscillations | LFP, local field potential
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3. Full Text Subthalamic Nucleus Stimulation in Severe Obsessive–Compulsive Disorder
by Mallet, Luc and Polosan, Mircea and Jaafari, Nematollah and Baup, Nicolas and Welter, Marie-Laure and Fontaine, Denys and Montcel, Sophie Tezenas du and Yelnik, Jérôme and Chéreau, Isabelle and Arbus, Christophe and Raoul, Sylvie and Aouizerate, Bruno and Damier, Philippe and Chabardès, Stephan and Czernecki, Virginie and Ardouin, Claire and Krebs, Marie-Odile and Bardinet, Eric and Chaynes, Patrick and Burbaud, Pierre and Cornu, Philippe and Derost, Philippe and Bougerol, Thierry and Bataille, Benoit and Mattei, Vianney and Dormont, Didier and Devaux, Bertrand and Vérin, Marc and Houeto, Jean-Luc and Pollak, Pierre and Benabid, Alim-Louis and Agid, Yves and Krack, Paul and Millet, Bruno and Pelissolo, Antoine and STOC Study Grp and STOC Study Group
The New England journal of medicine, ISSN 0028-4793, 11/2008, Volume 359, Issue 20, pp. 2121 - 2134
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | General aspects | Anxiety disorders. Neuroses | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Psychopathology. Psychiatry | Biological and medical sciences | Medical sciences | Obsessive-compulsive disorders | Cross-Over Studies | Subthalamic Nucleus | Double-Blind Method | Electric Stimulation Therapy - adverse effects | Humans | Middle Aged | Obsessive-Compulsive Disorder - therapy | Adult | Female | Male | Infection - etiology | Cerebral Hemorrhage - etiology | Care and treatment | Obsessive-compulsive disorder | Diagnosis | Risk factors | Nuclear magnetic resonance--NMR | Behavior modification | Neuroses | Parkinsons disease | Index Medicus | Abridged Index Medicus | Computer Science | Medical Imaging
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4. Full Text Long‐term plasticity of glutamatergic input from the subthalamic nucleus to the entopeduncular nucleus
by Gorodetski, Lilach and Zeira, Reut and Lavian, Hagar and Korngreen, Alon
The European journal of neuroscience, ISSN 0953-816X, 09/2018, Volume 48, Issue 5, pp. 2139 - 2151
long‐term plasticity | basal ganglia | entopeduncular nucleus | subthalamic nucleus | glutamate receptors | long-term plasticity | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Rats, Wistar | Synapses - physiology | Basal Ganglia - physiology | Neural Pathways - physiology | Action Potentials - physiology | Subthalamic Nucleus - physiology | Entopeduncular Nucleus - physiology | Animals | Neuronal Plasticity - physiology | Time Factors | Neurons - physiology | Corpus Striatum - physiology | Substantia Nigra - physiology | Glutamate | Neurons | Basal ganglia | Animal models | Brain slice preparation | Substantia nigra | Long-term potentiation | Cortex | Solitary tract nucleus | Action potential | Neurogenesis | Electrical stimuli | Cannabinoids | Neostriatum | Synaptic plasticity | Calcium buffering | Synaptic depression | Thalamus | Subthalamic nucleus | Glutamatergic transmission | Index Medicus
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5. Full Text Subthalamic nucleus—sensorimotor cortex functional connectivity in de novo and moderate Parkinson's disease
by Kurani, Ajay S and Seidler, Rachael D and Burciu, Roxana G and Comella, Cynthia L and Corcos, Daniel M and Okun, Michael S and MacKinnon, Colum D and Vaillancourt, David E
Neurobiology of aging, ISSN 0197-4580, 2015, Volume 36, Issue 1, pp. 462 - 469
Neurology | Internal Medicine | Drug naive | Connectivity | Subthalamic nucleus | Parkinson's disease | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Geriatrics & Gerontology | Science & Technology | Severity of Illness Index | Parkinson Disease - pathology | Humans | Middle Aged | Male | Parkinson Disease - physiopathology | Case-Control Studies | Sensorimotor Cortex - physiopathology | Synaptic Transmission | Magnetic Resonance Imaging | Subthalamic Nucleus - pathology | Subthalamic Nucleus - physiology | Female | Aged | Sensorimotor Cortex - pathology | Diagnostic imaging | Antiparkinsonian agents | Index Medicus
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6. Globus pallidus interna or subthalamic nucleus deep brain stimulation for Parkinson disease a review
by Ramirez-Zamora, Adolfo and Ostrem, Jill L
JAMA neurology, ISSN 2168-6149, 03/2018, Volume 75, Issue 3, pp. 367 - 372
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Parkinson Disease - therapy | Subthalamic Nucleus - physiology | Humans | Globus Pallidus - physiology | Deep Brain Stimulation - methods
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7. Full Text Subthalamic nucleus deep brain stimulation in isolated dystonia: A 3-year follow-up study
by Ostrem, Jill L and San Luciano, Marta and Dodenhoff, Kristen A and Ziman, Nathan and Markun, Leslie C and Racine, Caroline A and de Hemptinne, Coralie and Volz, Monica M and Heath, Susan L and Starr, Philip A
Neurology, ISSN 0028-3878, 11/2016, Volume 88, Issue 1, pp. 25 - 35
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Dystonia - therapy | Severity of Illness Index | Humans | Middle Aged | Male | Treatment Outcome | Deep Brain Stimulation - methods | Neuropsychological Tests | Young Adult | Subthalamic Nucleus - physiology | Time Factors | Adolescent | Adult | Female | Aged | Cohort Studies | Index Medicus | Abridged Index Medicus
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8. Full Text Subthalamic nucleus‐deep brain stimulation for early motor complications in Parkinson's disease—the EARLYSTIM trial: Early is not always better
by Mestre, Tiago A and Espay, Alberto J and Marras, Connie and Eckman, Mark H and Pollak, Pierre and Lang, Anthony E
Movement disorders, ISSN 0885-3185, 12/2014, Volume 29, Issue 14, pp. 1751 - 1756
EARLYSTIM | Parkinson's disease | patient expectation | Subthalamic nucleus the brain stimulation | dyskinesia | motor complications | health economics | Health economics | Patient expectation | Motor complications | Dyskinesia | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Parkinson Disease - therapy | Subthalamic Nucleus - physiopathology | Humans | Deep Brain Stimulation | Treatment Outcome | Clinical Trials as Topic | Electric Stimulation Therapy | Parkinson Disease - physiopathology | Index Medicus
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