Dynamical Systems in Neuroscience:

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84 One-Dimensional Systemssteady-state current (pA)200-20-40-60I (V)(V sn , I sn )I sn -k(V-V sn )2I-V relation-60 -40 -20membrane potential, V (mV)Figure 3.34: Magnification of the I-V curve in Fig. 3.31 at the left knee shows that itcan be approximated by a square parabola.Considering infinite values of the membrane potential may be convenient from apurely mathematical point of view, but this has no physical meaning and no way tosimulate it on a digital computer. Instead, we fix a sufficiently large constant V peakand say that (3.9) generated a spike when V (t) reached V peak . After the peak of thespike is reached, we reset V (t) to a new value V reset . The topological normal form forthe saddle-node bifurcation with the after-spike resetting˙V = I + V 2 , if V ≥ V peak , then V ← V reset (3.10)is called the quadratic integrate-and-fire neuron. It is the simplest model of a spikingneuron. The name stems from its resemblance to the leaky integrate-and-fire neuron˙V = I −V considered in Chap. 8. In contrast to the common folklore, the leaky neuronis not a spiking model because it does not have a spike-generation mechanism, i.e., aregenerative up-stroke of the membrane potential, whereas the quadratic neuron does.We discuss this and other issues in detail in Chap. 8.In general, quadratic integrate-and-fire model could be derived directly from theequation C ˙V = I − I ∞ (V ) by approximating the steady-state I-V curve near theresting state by the square parabola I ∞ (V ) ≈ I sn − k(V − V sn ) 2 , where k > 0 andthe peak of the curve (V sn , I sn ) could be easily found experimentally; see Fig. 3.34.Approximating the I-V curve by other functions, for example I ∞ (V ) = g leak (V −V rest )−ke pV , results in other forms of the model, e.g., the exponential integrate-and-fire model(Fourcaud-Trocme et al. 2003), which has certain advantages over the quadratic form.Unfortunately, the model is not solvable analytically, and it is expensive to simulate.The form I ∞ (V ) = g leak (V −V leak )−k(V −V th ) 2 +, where x + = x when x > 0 and x + = 0otherwise, combines the advantages of both models. The parameters V peak and V resetare derived from the shape of the spike. Normalization of variables and parametersresults in the form (3.10) with V peak = 1.In Fig. 3.35 we simulated the quadratic integrate-and-fire neuron to illustrate a
One-Dimensional Systems 85000I 0, not shown in the figure, the membrane potential is reset to the right ofthe ghost, no slow transition is involved, and the tonic spiking starts with a non-zerofrequency. As an exercise, explain why there is a noticeable latency (delay) to the first
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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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134 Conductance-Based Models• If
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136 Conductance-Based Modelsinward(
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138 Conductance-Based Models1I=01I=
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140 Conductance-Based Modelsleak cu
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142 Conductance-Based Modelshyperpo
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144 Conductance-Based Models0I=0ina
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146 Conductance-Based Models0I=9.75
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148 Conductance-Based Models1I=651I
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150 Conductance-Based Modelshave co
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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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