ライフサイエンスコーパス: gyri

1 tcentral/superior parietal and supramarginal gyri).

2 ior temporal gyrus, and pre- and postcentral gyri.

3 oral cortex to the angular and supramarginal gyri.

4 al and medial temporal cortex, and cingulate gyri.

5 brain is strongly convoluted into sulci and gyri.

6 also within the middle and inferior frontal gyri.

7 in the left inferior frontal and postcentral gyri.

8 ctivated both the precentral and postcentral gyri.

9 te and both left fusiform and medial frontal gyri.

10 bolism in right superior and middle temporal gyri.

11 on the adjacent superior and middle temporal gyri.

12 anges in the hippocampus and parahippocampal gyri.

13 l and inferior frontal gyri and the temporal gyri.

14 ects the FG into lateral and medial parallel gyri.

15 boundary of the Middle and Superior Temporal Gyri.

16 regions, predominantly in the middle frontal gyri.

17 left superior, middle, and inferior temporal gyri.

18 le temporal, middle occipital and precentral gyri.

19 ards the superior temporal and supramarginal gyri.

20 ntified in the inferior frontal and fusiform gyri.

21 ule, including the supramarginal and angular gyri.

22 merous (poly) and noticeably smaller (micro) gyri.

23 tion of the left inferior and middle frontal gyri.

24 ecific for areas in the lingual and fusiform gyri.

25 tal, anterior cingulate, and parahippocampal gyri.

26 right mid-frontal, and left inferior frontal gyri.

27 right superior frontal and inferior parietal gyri.

28 amygdala and the hippocampal/parahippocampal gyri.

29 mporal cortices, including superior temporal gyri.

30 t (P=.003) and right (P=.012) middle frontal gyri.

31 al regions, cingulate and lateral precentral gyri.

32 panied by folding of the cortical sheet into gyri.

33 s cortical size and induces folds resembling gyri.

34 lear speech activated both anterior fusiform gyri.

35 l, superior and middle temporal, and lingual gyri.

36 uctuations between left and right precentral gyri.

37 al morphometric measurements of the affected gyri.

38 th better L&M performance and larger dentate gyri.

39 frontal cortex and the mid-inferior frontal gyri.

40 frontal cortex and the angular and cingulate gyri.

41 the medial and ventromedial superior frontal gyri.

42 ter growth speed could consistently engender gyri.

43 ferior occipital and right inferior temporal gyri.

44 oral cortex, and inferior and middle frontal gyri.

45 l as the supramarginal and superior temporal gyri.

46 l areas, particularly the bilateral fusiform gyri.

47 ampal gyri, as well as the superior temporal gyri.

48 early cortical thickening was present on the gyri.

49 roup with the bilateral pre- and postcentral gyri.

50 ortical laminae, multiple cortical areas and gyri.

51 were also found within the pre/post-central gyri.

52 egion lying between the fusiform and lingual gyri.

53 t superior frontal and left middle occipital gyri.

54 the left superior (STG) and middle temporal gyri (16 voxels, CCLAV = 0.04) and increased creatine in

55 e patients, NAA was reduced in right frontal gyri (19 voxels, CCLAV = 0.05) and myo-inositol was redu

56 volving anterior middle temporal and angular gyri; a speech perception network involving superior tem

57 la and dorsal and ventral anterior cingulate gyri (ACG), regions important for attention to and perce

58 e bilateral anterior cingulate/paracingulate gyri (ACG/ApCG), left cerebellum (lobules IV/V and VIII)

59 d left inferior frontal and middle occipital gyri activity and correlated negatively with plasma ghre

60 aging, we show that small "bumps," or buried gyri, along the lower bank of the superior temporal sulc

61 The gyrI (also called sbmC) gene product inhibits DNA gyrase

62 haracterized by an excessive number of small gyri and abnormal cortical lamination.

63 ctivation in the middle and inferior frontal gyri and anterior cingulate gyrus, in addition to region

64 in inferior prefrontal and superior temporal gyri and cerebellum.

65 ntal lobes, including cingulate and fusiform gyri and cerebellum.

66 Cortical folding, characterized by convex gyri and concave sulci, has an intrinsic relationship to

67 isphere middle temporal and inferior frontal gyri and decreased activity in right inferotemporal cort

68 toencephalography revealed enlarged Heschl's gyri and enhanced right-left hemispheric synchronization

69 children showed reduced volumes of Heschl's gyri and enhanced volumes of the plana temporalia that w

70 cited activation in the lingual and fusiform gyri and in the Brodmann areas 22 and 38 in superior tem

71 ula, and parahippocampal and middle temporal gyri and in the left inferior frontal and postcentral gy

72 The first, localized to bilateral Heschl's gyri and indexed by low-frequency phase, predicts the ti

73 ce of a circuit between left middle temporal gyri and inferior frontal gyrus for both groups.

74 luding the left superior and middle temporal gyri and inferior frontal gyrus, and there was no signif

75 olumes in the left and right middle temporal gyri and left posterior superior temporal gyrus were pre

76 ination; (ii) left superior-/middle-temporal gyri and receptive aphasia; (iii) widespread temporal/fr

77 d GMV in the caudate, thalamus, and fusiform gyri and reduced GMV in the cerebellar vermis in FXS at

78 because VBM analysis includes both cortical gyri and sulci as a single GM region.

79 nduced the formation of prominent, bilateral gyri and sulci in the rostrolateral neocortex.

80 similar to the macroscopic appearance of the gyri and sulci of the human brain.

81 maging revealed only an irregular pattern of gyri and sulci, for which we propose the term tubulinopa

82 ating that this folding, which gives rise to gyri and sulci, is subject to major changes during prima

83 oduction of neuroepithelial folds resembling gyri and sulci, which are not normally present in avian

84 in the cortex is coupled to the formation of gyri and sulci.SIGNIFICANCE STATEMENT Abnormal brain mor

85 yrus, posterior middle and superior temporal gyri and superior temporal sulcus, as well as the white

86 ted in premotor cortex, pre- and postcentral gyri and supramarginal gyrus with minimal extension into

87 nts in the left inferior and middle temporal gyri and the left middle occipital gyrus (ROI depression

88 cluded the right and left inferior occipital gyri and the right middle occipital gyrus, right inferio

89 ng the superior, medial and inferior frontal gyri and the temporal gyri.

90 ons in the left middle and superior temporal gyri and to the inferior parietal lobe was a predictor o

91 indicate variations in the shape of parietal gyri and white matter microstructural anomalies of the t

92 x (DLPFC) (i.e., middle and superior frontal gyri) and insula GMVs were associated with increased alc

93 ved the prefrontal (gyrus rectus and orbital gyri) and then postcentral neocortex and striatum.

94 al gyri, bilateral middle occipital/fusiform gyri, and bilateral cerebella for both the rhyming and m

95 s the bilateral posterior cingulate, lingual gyri, and cerebellum that showed greater GMV in the cann

96 posterior cingulate cortex, parahippocampal gyri, and frontal pole, that exhibited activity uniquely

97 rtex, amygdala, middle and inferior temporal gyri, and fusiform gyrus the most severely damaged.

98 t posterior parahippocampal and mid-fusiform gyri, and in the hippocampal body in healthy young indiv

99 hippocampus and parahippocampal and fusiform gyri, and increasing activation in the posteromedial cor

100 l cortices, anterior cingulate/paracingulate gyri, and inferior parietal cortices, as well as the lef

101 rea (SMA), frontal operculum, middle frontal gyri, and inferior parietal lobule were specifically ass

102 l, right superior and left inferior temporal gyri, and left superior parietal lobule.

103 uperior frontal and right anterior cingulate gyri, and left thalamus.

104 eocortical delineations were done for sulci, gyri, and modified Brodmann areas to link macroscopic an

105 emporal (T = 4.25) and precentral (T = 6.47) gyri, and one right ILF end point, the occipital lobe (T

106 ocampus, supramarginal and inferior temporal gyri, and posterior cerebellum, with decreased activity

107 or hippocampus, parahippocampal and fusiform gyri, and predominantly left hemisphere extra-temporal a

108 claustrum, right middle and inferior frontal gyri, and right angular gyrus.

109 gyrus, bilateral middle and inferior frontal gyri, and right precuneus.

110 totopically on ventral pre- and post-central gyri, and that partially overlap at individual electrode

111 rolateral prefrontal gyri, superior temporal gyri, and the putamen (p < .001).

112 ral orbitofrontal gyrus and inferior frontal gyri, and the rostral anterior cingulate cortex.

113 ions of the cortical surface: the sulci, the gyri, and the straight bank region, which is interposed.

114 network in the superior and middle temporal gyri; and atrophy of anterior components of the face and

115 comparison group in the bilateral precentral gyri, anterior cingulate cortex, and middle and superior

116 he thalamus, cingulate cortices, and angular gyri are fundamental for human consciousness.

117 o faces, whereas the parahippocampal/lingual gyri are more responsive to buildings.

118 s have clearly established that the fusiform gyri are preferentially responsive to faces, whereas the

119 ace of the cortex, where normally convoluted gyri are replaced by numerous (poly) and noticeably smal

120 The transverse gyri are thought to be established in utero; our results

121 unction was observed in the pre/post-central gyri as expected.

122 , and inferior temporal and superior orbital gyri as the biomarker components.

123 ate cortex, and middle and superior temporal gyri as well as greater activation relative to both comp

124 thickness of left angular and supramarginal gyri as well as the left lateral occipital cortex.

125 mpus, thalamus, fusiform and middle temporal gyri, as well as the left and right insula, for those wi

126 nar nuclei of the thalamus, and the fusiform gyri, as well as the medial and lateral dorsal and ventr

127 odels involved the bilateral parahippocampal gyri, as well as the superior temporal gyri.

128 ing, such as the inferior and middle frontal gyri, as well as the supramarginal and superior temporal

129 erosis across the cortical width, sulci, and gyri; (b) their relation with white matter lesion accrua

130 ed activation in bilateral superior temporal gyri (BA 42 and 22), a region associated with phonologic

131 o increased size in FXS, such as the orbital gyri, basal forebrain, and thalamus, suggests delayed or

132 interest were drawn in pre- and postcentral gyri based on anatomic criteria.

133 , the right inferior and left medial frontal gyri (beta = 0.75 vs. 0.54), and the left thalamus (beta

134 men, right middle occipital/ middle temporal gyri, bilateral cingulate gyrus and right sensorimotor a

135 d activation in left inferior/middle frontal gyri, bilateral medial frontal gyri, bilateral middle oc

136 iddle frontal gyri, bilateral medial frontal gyri, bilateral middle occipital/fusiform gyri, and bila

137 for generate>read in inferior/middle frontal gyri bilaterally (L>R), anterior cingulate, and caudate

138 frontal cortex's superior and middle frontal gyri bilaterally and in the left occipital lobe as a con

139 ral activations within the superior temporal gyri bilaterally and no increased extra-temporal areas o

140 or middle temporal, and inferior postcentral gyri bilaterally, and enlarged superior frontal gyrus, g

141 er fell secondarily on core and intermediate gyri but, overall, was preserved on the outer (upper lev

142 cting both the cingulate and parahippocampal gyri, but also the limbic and visual cortices.

143 Activation of fusiform gyri by faces was strongly affected by attentional condi

144 sylvian fissure and temporal and postcentral gyri, by using magnetic resonance data and a novel surfa

145 a also suggest that the position of cortical gyri can be molecularly specified in mice.

146 ng to inferior frontal and superior temporal gyri, caudate, and other structures is affirmed.

147 tivation in left inferior and middle frontal gyri, caudate, and thalamus.

148 decreased FA in the genu, cingulum cingulate gyri, centrum semiovale, inferior longitudinal fasciculi

149 ions (mostly the middle and inferior frontal gyri, cingulate, and insula) showed significant LR group

150 activation in superior temporal and frontal gyri, cingulate, thalamus, and basal ganglia.

151 also cingulate, paracentral, and precentral gyri, compared with the non-hallucinators.

152 the visual field tends to be represented on gyri (convex folds), whereas the horizontal meridian is

153 vity in the precentral and superior temporal gyri correlated with posttreatment symptom improvement.

154 the medial frontal, temporal, and cingulate gyri correlated with severity of positive symptoms.

155 Left middle temporal gyri correlated with task accuracy for both groups.

156 posterosuperior, middle temporal and angular gyri corresponding to Wernicke's area.

157 ation in motor regions (bilateral precentral gyri, corticospinal tracts, and the corpus callosum) of

158 eral prefrontal cortex and superior temporal gyri, deficit regions found consistently in adult studie

159 mplex, the parahippocampal, and the fusiform gyri did not predict target presence, while high-level a

160 al cortex, as well as precentral/postcentral gyri during processing of threatening faces predicted gr

161 emporal, supramarginal, and superior frontal gyri during reappraisal were among the best predictors,

162 effect that was visible at the neighbouring gyri (e.g., knock-on effect at the SFG following CG defi

163 r region, delineated by the limiting insular gyri, expanded to a much lesser degree.

164 , bilaterally in the middle frontal/premotor gyri, extending down the medial prefrontal wall to the a

165 tion caused decreased activation in fusiform gyri for angry faces and decreased ratings of happiness

166 for all contacts), (2) the anatomy of insula gyri (for 20 vestibular sites), and (3) the probabilisti

167 We also examined dentate gyri from epileptic human hippocampal surgical specimens

168 initial values and rates of change higher in gyri, frontal and temporal poles, and parietal cortex; a

169 recentral gyrus, middle and superior frontal gyri, frontal pole, and cingulate gyrus in S-allele carr

170 However, the middle and inferior temporal gyri have received little investigation, especially in f

171 ions within the superior and middle temporal gyri, hippocampus, and LIFG were insensitive to the acou

172 percent neuronal commitments in the dentate gyri however, were not significantly different from cont

173 thin the bilateral anterior interior frontal gyri (IFG), left posterior IFG, SMG, and posterior cingu

174 and from U-shaped fibres connecting adjacent gyri; (iii) it arises in extrastriate visual 'associatio

175 e bilateral superior-temporal and precentral gyri immediately following question onset; at the same t

176 the inferior, middle, and superior temporal gyri in 20 patients with first-episode schizophrenia, 20

177 , hippocampus, parahippocampal, and fusiform gyri in 30 of 31 subjects compared with normal eye image

178 The cingulate gyri in 37 subjects with and without early dementia of t

179 n amplitude across the pre- and post-central gyri in a diffuse manner that is not finger-specific.

180 farct of the right angular and supramarginal gyri in a setting of chronic migraine.

181 activation in the pSTS and inferior frontal gyri in CM than in AM.

182 ey role of listener's left superior temporal gyri in extracting the slow approximately 0.5 Hz modulat

183 me in the right superior and middle temporal gyri in nonrecovered amusic patients compared with nonam

184 ter decreases in superior and medial frontal gyri in participants with hearing loss compared to norma

185 in the left inferior frontal and precentral gyri in subjects who remain well.

186 ly to have multiple or split left transverse gyri in the auditory cortex than nonexpert controls, and

187 ility along the superior and middle temporal gyri in the left hemisphere and in a less-extensive homo

188 en sgACC and the middle and inferior frontal gyri in the MDD group.

189 h cerebral hemispheres except for precentral gyri in the second one.

190 of the core with respect to major sulci and gyri in the superior temporal region varied most in the

191 comprehension in bilateral superior temporal gyri (including primary auditory cortex), thalamus, and

192 activation in inferior and superior frontal gyri, including dorsolateral prefrontal cortex and ventr

193 onse in medial prefrontal cortex and angular gyri increased linearly with the probability of the curr

194 r shift of the inferior pre- and postcentral gyri, indicative of reorganization of the frontal opercu

195 activated voxels in the pre- and postcentral gyri induced by active and passive movements was compare

196 n, parahippocampal, lingual, middle temporal gyri, inferior and superior parietal lobules and precune

197 l cortex, right superior and middle temporal gyri, insula, right posterior cingulate cortex, lingual

198 al sulci, amygdala, and the inferior frontal gyri/insula, targets evoked stronger responses than dist

199 ) and the left dorsolateral superior frontal gyri (item-gamma) on permutation test, where the couplin

200 cingulate (cue-alpha) and the left fusiform gyri (item-gamma).

201 including dorsal superior and middle frontal gyri, lateral and medial orbitofrontal gyri, right anter

202 We found that within the inferior occipital gyri, lateral fusiform gyri, superior temporal sulci, am

203 sely, participants with larger left Heschl's gyri learned consonantal or tonal contrasts faster than

204 lated happiness network included postcentral gyri, left caudate, right cingulate cortex, right superi

205 ent in the left superior and middle temporal gyri, left inferior parietal region with postcentral gyr

206 left middle and bilateral inferior temporal gyri, left parahippocampal area, left geniculum body, le

207 right inferior temporal and middle occipital gyri, left precentral gyrus, bilateral opercular part of

208 GyrI-like proteins are widely distributed in prokaryotes

209 gs suggest that the evolutionarily conserved GyrI-like proteins confer cellular protection against di

210 Convoluted cortical gyri-like structures characterize the mushroom body caly

211 umes of left and right lateral orbitofrontal gyri (LOFG), left superior temporal gyrus, and right ins

212 temporal lobe (superior and middle temporal gyri) may be specific to schizophrenia, whereas smaller

213 re obtained in superior and inferior frontal gyri, medial and lateral orbitofrontal cortex, and parah

214 in the middle frontal and inferior temporal gyri (MFG and ITG) and resistant (cerebellum) to classic

215 ferences in the cuneus, lingual and fusiform gyri, middle occipital lobe, inferior parietal lobule, a

216 ppocampal gyrus, inferior and middle frontal gyri, middle temporal gyrus, and lingual gyrus.

217 ions of the left and right superior temporal gyri (mSTG).

218 In the insula, precentral and postcentral gyri NTDE signals were greater, and PTDE-related functio

219 surface area and folds resembling sulci and gyri of higher mammals.

220 parietal gyrus and supramarginal and angular gyri of the inferior parietal lobe), right precuneus, an

221 middle frontal, middle temporal, and angular gyri of the left hemisphere and the lingual and inferior

222 g-form PDE4D isoforms into bilateral dentate gyri of the mouse hippocampus downregulated PDE4D4 and P

223 sphere and the lingual and inferior temporal gyri of the right hemisphere and regression of participa

224 tor proliferation in the hippocampal dentate gyri of wild-type adult mouse brains.

225 tronger in specific orientations relative to gyri or sulci.

226 the superior frontal and anterior cingulate gyri (P > 0.01).

227 and FA values in the cerebellum and fusiform gyri (P < .05).

228 nt of the prefrontal, temporal, and parietal gyri (P < .05, false discovery rate corrected).

229 nding into the bilateral posterior cingulate gyri (P <.001) and left (P=.003) and right (P=.012) midd

230 .001), bilateral superior and middle frontal gyri (P <.001), and left inferior parietal lobe (P=.007)

231 nding into the bilateral posterior cingulate gyri (P <.001), bilateral superior and middle frontal gy

232 ation in precentral (P<.001) and postcentral gyri (P = .03) and the cerebellum (P<.001), although 3 B

233 ddle frontal (P = 0.002) and middle temporal gyri (P = 0.033) and transentorhinal (P = 0.005) and ant

234 ., dorsolateral prefrontal and supramarginal gyri; p = 0.010) and reduced suppression of activation i

235 ight inferior, middle, and superior temporal gyri (PFWE < 0.05); right temporal pole, anterior hippoc

236 nal connectivity of the bilateral precentral gyri positively correlated with fractional anisotropy va

237 resulted in greater deactivation in fusiform gyri, possibly reflecting greater suppression of visual

238 c nodes of the default mode network (angular gyri, posterior cingulate, and medial prefrontal cortex)

239 basal forebrain, cingulate and paracingulate gyri, posterior supramarginal gyrus, and planum temporal

240 ly engaged the superior frontal and parietal gyri, precentral gyrus, and the caudate.

241 ae, cingulate cortices, pre- and postcentral gyri, precunei, cunei, bilateral putamena, right pallidu

242 activity in the inferior and middle frontal gyri, precuneus, cingulate cortex, caudate, and postcent

243 this relationship at the level of individual gyri provides additional evidence of differences in the

244 er grey matter volume of the parahippocampal gyri (r(s) =-0.31, p=0.004).

245 h activity in right superior/middle temporal gyri regardless of tissue integrity.

246 sponse in the left angular and supramarginal gyri, regions that play important roles in linguistic pr

247 nodal centralities in left pre-/postcentral gyri relative to controls.

248 or cingulate and superior and medial frontal gyri relative to those with hearing loss and tinnitus.

249 icularly the inferior occipital and fusiform gyri, remained selective despite showing only 9%-25% of

250 n the core, intermediate and outer penumbral gyri, respectively.

251 erally in the parietal region (supramarginal gyri), right posterior cingulate gyrus, and left occipit

252 ontal gyri, lateral and medial orbitofrontal gyri, right anterior insula, putamen, thalamus, and caud

253 p in the left and right laterodorsal frontal gyri, right medial prefrontal cortex, right superior and

254 re found in left medial and inferior frontal gyri, right precuneus, left inferior parietal lobule, an

255 brain regions, including MT or V5, fusiform gyri, right premotor cortex, and the intraparietal sulci

256 formation of the precentral and postcentral gyri, right superior temporal gyrus, and opercula, which

257 refrontal cortices, and the superior frontal gyri, right ventrolateral prefrontal cortex, the dorsal

258 right inferior, middle, and superior frontal gyri (ROI compensation).

259 vs. 1.48, P < 0.001) and posterior cingulate gyri ROIs (1.63 vs. 1.72, P < 0.001).

260 to the formation of cusped sulci and smooth gyri similar to those in the brain.

261 rietal lobule (SPL), and right supramarginal gyri (SMG).

262 al (PostCG) and the superior occipital (SOG) gyri, suggesting complex visual processing in this netwo

263 ts noted the cortex is thinner in sulci than gyri, suggesting that development may occur on a fine sc

264 d and consistent by presenting an intriguing gyri-sulci formation comparison.

265 ions are centered near-but distinct from-the gyri/sulci for which they were originally named.

266 s incorporating precentral and supramarginal gyri, superior temporal cortex, central operculum/poster

267 bilateral insulae, ventrolateral prefrontal gyri, superior temporal gyri, and the putamen (p < .001)

268 he inferior occipital gyri, lateral fusiform gyri, superior temporal sulci, amygdala, and the inferio

269 ala; superior, middle, and inferior temporal gyri; superior parietal lobe; and posterior cingulate gy

270 ng bilateral STG, precentral and postcentral gyri, supplementary motor area, supramarginal gyrus, pos

271 bilinguals have, on average, larger Heschl's gyri than monolinguals.

272 Mean diffusivity was higher in gyri than sulci and in frontal compared with occipital l

273 ons (ie, supramarginal and superior parietal gyri) that merit further investigation.

274 While located in the ectosylvian gyri, the auditory cortex includes several areas, resemb

275 he amygdala, the hippocampal/parahippocampal gyri, the dorsomedial/pulvinar nuclei of the thalamus, a

276 reas such as the superior and middle frontal gyri, the insula, and the occipital cortex.

277 gulate cortex, the left and right precentral gyri, the left and right anterior temporal cortices, and

278 the superior, middle, and inferior temporal gyri, the left posterior superior temporal gyrus gray ma

279 ior frontal, inferior parietal, and fusiform gyri; the precuneus; and the dorsomedial prefrontal cort

280 strong in the inferior temporal and fusiform gyri, two areas important for object recognition.

281 pathologies, although precentral/postcentral gyri volume was reduced in comparison with other patholo

282 d significantly less bilateral orbitofrontal gyri volume, higher functional connectivity in the orbit

283 ation in the left and right inferior frontal gyri was determined with respect to the anatomical sub-r

284 activity in left inferior and middle frontal gyri was observed when comparing words with partwords an

285 m, insula, and inferior and superior frontal gyri was positively related to the motion speed of dot p

286 FA in the parahippocampal gyri was significantly decreased in patients with sleep

287 forms the boundaries of major orbitofrontal gyri, was classified into three types (Type I, II and II

288 the superior, inferior, and middle temporal gyri were atrophic, and subjacent white matter was gliot

289 in the left postcentral and middle occipital gyri were found only in older maltreated individuals rel

290 umes of the left and right superior temporal gyri were measured using magnetic resonance imaging obta

291 right insular, lingual and superior parietal gyri were significantly smaller, on average, in PTSD pat

292 vated in the left and right inferior frontal gyri when performing a covert verb generation task.

293 tion in left inferior frontal and precentral gyri, whereas a SNP at the KIAA0319/TTRAP/THEM2 locus wa

294 h interactions in medial frontal and lingual gyri, whereas processing of happy faces was associated w

295 Hz to the activity of both superior temporal gyri, whereas the modulations at 4-8 Hz were coupled to

296 eased in width and produced folds resembling gyri, which are not normally present in mouse brains and

297 lateral temporal, angular, and supramarginal gyri, which have previously been implicated in autism in

298 The pattern of sulci and gyri, while simple, appears very similar to that observe

299 ng of the cortical mantle resulting in small gyri with a fused surface.

300 cts including enlarged cerebella and dentate gyri with increased size of neuronal nuclei and somata,