Dynamical Systems in Neuroscience:

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102 Two-Dimensional Systems0.70.6K + activation variable, n0.50.40.3n-nullclineV-nullcline0.20.1membrane voltage, V (mV)00-20-40-60-80 -70 -60 -50 -40 -30 -20 -10 0 10 20membrane voltage, V (mV)-800 5 10 15 20 25 30time (ms)Figure 4.10: Stable limit cycle in the I Na,p +I K -model (4.1, 4.2) with low-threshold K +current and I = 40.
Two-Dimensional Systems 103derivative, V' (mV/ms)membranepotential (mV)2001000-100-80 -60 -40 -20 0 20 40membrane potential, V (mV)40200-20-40cortical pyramidal neuron cortical interneuron brainstem neuron-600 50 100-80 -60 -40 -20 0 20 40membrane potential, V (mV)-80 -60 -40 -20 0 20 40membrane potential, V (mV)0 20 40 60 0 10 20time (ms)Figure 4.11: Limit cycles corresponding to tonic spiking of three types of neuronsrecorded in vitro.ẏ = µg(x, y) (slow variable)where small parameter µ describes the ratio of time scales of variables x and y. Typically,fast variable x has a cubic-like nullcline that intersects the y-nullcline somewherein the middle branch, as in Fig. 4.12a, resulting in relaxation oscillations. The periodictrajectory of the system slides down along the left (stable) branch of the cubic nullclineuntil it reaches the left knee A. At this moment, it quickly jumps to the point B andthen slowly slides up along the right (also stable) branch of the cubic nullcline. Uponreaching the right knee C, the system jumps to the left branch and starts to slide downagain, thereby completing one oscillation. Relaxation oscillations are easy to graspconceptually, but some of their features are quite difficult to study mathematically.We consider relaxation oscillations in detail in Sect. 6.3.4.Notice that the jumps in Fig. 4.12a are nearly horizontal — a distinctive signature ofrelaxation oscillations that is due to the disparately different time scales in the system.Although many neuronal models have fast and slow time scales and could be reducedto the fast/slow form above, they do not exhibit relaxation oscillations because theparameter µ is not small enough. Anybody who records from neurons would probablynotice the weird square shape of “spikes” in Fig. 4.12b, something that most biologicalneurons do not exhibit. Nevertheless, relaxation oscillations in fast/slow systems areimportant when we consider neuronal bursting in Chap. 9, though the fast variable xis two-dimensional there.
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Eugene M. IzhikevichThe Neuroscienc
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6.3.6 Saddle-node homoclinic orbit
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9.4.2 Integrators vs. Resonators .
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xPrefaceversely, cells having quite
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2 Introductionapical dendritessomar
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4 Introduction(a)spikes(b)spikes cu
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6 Introduction1.1.3 Why are neurons
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8 Introductionconcepts of dynamical
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10 Introductionspikingmoderesting m
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12 Introduction(a)spikinglimitcycle
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14 Introductionco-existence of rest
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16 Introduction1.2.4 Neuro-computat
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18 IntroductionspikeFigure 1.16: Ph
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20 Introductionwith coupled neurons
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22 IntroductionFigure 1.17: John Ri
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24 Introduction
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26 Electrophysiology of NeuronsInsi
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28 Electrophysiology of Neuronsouts
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30 Electrophysiology of NeuronsRest
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32 Electrophysiology of NeuronsFigu
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34 Electrophysiology of Neuronsm (V
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36 Electrophysiology of Neurons10.8
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38 Electrophysiology of Neurons2.3
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42 Electrophysiology of NeuronsDepo
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44 Electrophysiology of NeuronsV(x,
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46 Electrophysiology of Neurons1m (
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48 Electrophysiology of NeuronsPara
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152 Conductance-Based Models1 sec10
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154 Conductance-Based Modelsvoltage
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156 Conductance-Based Models1h=0.89
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158 Conductance-Based Models5.2.2 E
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160 Conductance-Based Models1recove
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162 Conductance-Based Modelscurrent
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164 Conductance-Based Modelsmodels
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166 Conductance-Based Models
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168 Bifurcationssaddle-node bifurca
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170 Bifurcationssaddle-node bifurca
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172 Bifurcations0.5v 2V-nullclineK
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174 BifurcationsBoth types of the b
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176 BifurcationsV-nullcline0.5K + g
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178 Bifurcationsrstable limit cycle
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180 BifurcationsnVstable limit cycl
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¡ ¡¡ ¡¡ ¡ ¡¡ ¡ ¡182 Bifur
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¡ ¡ ¡¡ ¡ ¡¡ ¡ ¡¡ ¡ ¡184
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186 Bifurcationsmembrane potential,
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188 BifurcationsBifurcation of a li
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190 Bifurcationsstableunstablelimit
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192 Bifurcationsamplitude (max-min)
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194 Bifurcationshomoclinic orbithom
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196 Bifurcations0.80.60.4stable lim
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198 Bifurcationsfrequency (Hz)40030
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200 BifurcationsSaddle-Focus Homocl
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202 Bifurcationsc 1c 2xFigure 6.34:
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204 BifurcationseigenvaluesHopffold
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206 Bifurcationsfast nullclineslow
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208 Bifurcationswith fast and slow
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210 BifurcationsSupercritical Andro
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212 BifurcationsK + conductance tim
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214 BifurcationsIn contrast, if the
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216 Bifurcationsinvariant circlesad
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218 Bifurcationsbifurcationssaddle-
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220 BifurcationsExercises1. (Transc
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222 Bifurcationsv 2v 11a-11-1Figure
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224 Bifurcations19. [M.S.] A leaky
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226 Excitabilityspike?spikerestrest
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228 ExcitabilityAlternatively, the
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230 Excitability50 ms 20 mV 1 ms100
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232 ExcitabilityClass 3 excitable n
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234 Excitability0.20.150.10.05I 1I
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236 Excitabilitysaddle-node bifurca
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238 Excitability(a) resting spiking
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240 Excitabilityproperties integrat
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242 ExcitabilityThe existence of fa
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244 Excitability1coincidencedetecti
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246 Excitabilityspikeexcitatory pul
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248 Excitability(g)9 ms(f)(e)(d)(c)
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250 Excitabilitysquid axonmodel0 mV
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252 Excitability(a) integrator(b) r
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254 Excitability(a) integrator(b) r
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256 Excitabilitymembrane potential,
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258 Excitability0.1saddle-node bifu
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260 Excitability100 ms10 mVoscillat
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262 ExcitabilityBogdanov-Takens bif
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264 Excitabilitya pulse of current.
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266 Excitabilitymembrane potential
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268 Excitability(a)150100I K(M)(b)3
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270 Excitability50 mV300 msFigure 7
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272 Excitability20 mVADP100 msAHP-6
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274 ExcitabilityK + activation gate
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276 ExcitabilityBibliographical Not
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278 Excitability7. Show that the re
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280 Simple Modelsspikemembrane pote
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282 Simple Models1thresholdyz reset
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284 Simple Models1v reset =|b| 1/2b
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286 Simple Modelsbe an integrator o
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288 Simple Modelsintegrate-and-fire
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290 Simple Models(A) tonic spiking(
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292 Simple Modelsgeneral algorithm
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294 Simple Modelscha, cha — real
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296 Simple Modelslayer 5 neuronsimp
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298 Simple Modelsb=-240200saddle-no
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300 Simple Models(a)simple modellay
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302 Simple Models(a)burstingspiking
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304 Simple Models(a)dendriticspike2
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306 Simple Models(a)74 5 6 3210(b)C
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308 Simple Modelschattering neuron
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310 Simple ModelsLTS neuron (in vit
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312 Simple ModelsFS neuron (in vitr
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314 Simple Models(1) fast oscillati
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316 Simple Modelsthrough an appropr
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318 Simple Modelsthey are able to g
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320 Simple Modelsv r = −80 mV, an
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322 Simple Modelsshow in Fig. 7.36.
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324 Simple ModelsBibliographical No
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326 Simple ModelsExercises1. (Integ
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328 Simple Models17. [M.S.] Analyze
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330 Simple Modelsa35 mV350 msc-NAC
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332 Simple Modelsrat RTN neuronsimp
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334 Simple ModelsFigure 8.34: Class
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336 Simple Modelsspiny neuronlatenc
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338 Simple Models(a)stellate cellof
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340 Simple Modelsrat's mitral cell
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342 Bursting(a) cortical chattering
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344 Burstingmembranepotential (mV)-
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346 Burstingvoltage-gatedCa2+-gated
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348 Burstingslow dynamicsneuronvolt
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350 Burstingslow inactivation of in
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352 Bursting9.2.1 Fast-slow burster
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354 Burstingn-nullclinen slow =-0.0
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356 Bursting0maxmembrane potential,
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358 Bursting0membrane potential, V
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360 BurstingI=0I=4.5425 ms 25 mVI=5
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362 Burstingmembrane potential, V (
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364 Bursting9.3 ClassificationIn Fi
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366 Burstingbifurcation of spiking
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368 BurstingFigure 9.26: Putative
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370 Bursting108spikingslow variable
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372 Bursting(a)membrane potential,
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374 Burstingdepending on the type o
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376 BurstingsubcriticalAndronov-Hop
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378 Bursting(a)membrane potential,
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spiking380 Burstingfoldbifurcations
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382 BurstingspikingsupercriticalAnd
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384 Burstingaction potentials cut2
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386 Bursting9.4.3 BistabilitySuppos
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388 BurstingFigure 9.49: The instan
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esting390 Burstingspikesynchronizat
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392 BurstingReview of Important Con
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394 BurstingspikingrestingFigure 9.
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396 Bursting0-10membrane potential,
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398 Bursting0membrane potential, V
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400 BurstingFigure 9.61: A cycle-cy
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402 Bursting28. [Ph.D.] Develop an
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404 Synchronization (see www.izhike
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408 Solutions to Exercises, Chap. 3
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442 Referencesterneurons mediated b
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444 ReferencesDickson C.T., Magistr
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446 ReferencesGuckenheimer J. (1975
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448 Referencestional Journal of Bif
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450 ReferencesMarkram H, Toledo-Rod
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452 ReferencesRosenblum M.G. and Pi
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454 ReferencesTuckwell H.C. (1988)
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456 References9
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