ライフサイエンスコーパス: PPA

1 PPA provides a novel perspective that uniquely addresses

2 PPA was also shown to have the greatest affinity for the

3 Patients diagnosed with bvFTD (n=124), PPA (n=34) and CBS (n=85) were recruited.

4 object recognition and word processing in 20 PPA patients and 15 controls.

5 th P = 2.2 x 10(-8) [odds ratio (OR) = 1.22, PPA = 0.986].

6 We prospectively studied 25 PPA and 21 healthy individuals who underwent extensive c

7 al amyloid (Abeta(+) ) was found in 19 of 32 PPA patients.

8 The PPA-FTLD (n = 6), PPA-AD (n = 7), and AMN-AD (n = 6) groups did not differ

9 4) and 20p12.1 (OR = 1.20, P = 6.9 x 10(-7), PPA = 0.728).

10 omosomes 12q22 (OR = 1.16, P = 1.1 x 10(-7), PPA = 0.934) and 20p12.1 (OR = 1.20, P = 6.9 x 10(-7), P

11 object pairs matched with high accuracy (94% PPA group; 98% control group), but they failed to exhibi

12 A PPA describes the steps that people with tuberculosis ta

13 This paper summarizes the steps to conduct a PPA and serves as the basis for understanding country ca

14 Contrived specimens demonstrated a PPA between 95 and 100% and an NPA of 100% for all targe

15 The results of a PPA reveal programmatic gaps in care seeking, diagnosis,

16 CR reference method threshold cutoff, were a PPA of 62.1% (72 of 116 results; 95% CI, 52.6%-70.9%) an

17 amyloid burden was compared between Abeta(+) PPA and an Abeta(+) amnestic dementia groups (n = 22).

18 e entrapped in chitosan-polyphosphoric acid (PPA) beads.

19 graphene/graphite) in a polyphosphoric acid (PPA)/phosphorous pentoxide (P2 O5 ) medium are elucidate

20 d dioctanoyl glycerol pyrophosphatidic acid (PPA) also binds to the non-specific TMD region, but not

21 (di-n-octyl) dihydrogen pyrophosphonic acid (PPA).

22 aging (DTI) metrics to assess changes across PPA variants and perform brain-behavioral correlations.

23 ng, fluency, and sentence repetition) across PPA variants to better understand the anatomical substra

24 an autopsy-confirmed diagnosis of either AD (PPA-AD) or a tau variant of FTLD (PPA-FTLD) and 6 patien

25 ses were performed using pure TOPO and added PPA, and subsequent displacement experiments showed that

26 nstrated a positive percentage of agreement (PPA) between 60 and 100% for four targets (blaKPC, blaND

27 ence method, the positive percent agreement (PPA) (95% confidence interval [CI]), negative percent ag

28 The positive percent agreement (PPA) and negative percent agreement (NPA) between the TP

29 ture or EIA, the positive percent agreement (PPA) and negative percent agreement (NPA) values for the

30 rus assay showed positive percent agreement (PPA) and negative percent agreement (NPA) values of 98.3

31 al cultures, the positive percent agreement (PPA) of the BC-GN assay with the reference method was as

32 emonstrated a positive percentage agreement (PPA) of 91.1% (195 of 214 results; 95% confidence interv

33 Positive percent agreements (PPAs) and negative percent agreements (NPAs) of the PLEX

34 ing for renewable power purchase agreements (PPAs), displaced generation and capacity costs, and net

35 tanding cleft sentence structures, while all PPA variants and patients with bvFTD were impaired with

36 cterization of prephenate aminotransferases (PPA-ATs) that belong to class-Ib aspartate aminotransfer

37 ral (brachial) pulse pressure amplification (PPA) was calculated with the help of an arterial tonomet

38 K PEGylated-Pancreatic Polypeptide analogue (PPA) and 20K PEGylated-glucagon, we elucidated the decom

39 ional and regional patient pathway analyses (PPAs) were undertaken using existing national survey and

40 The patient-pathway analysis (PPA) is designed to assess the alignment between tubercu

41 The patient-pathway analysis (PPA) methodology detailed in this article was developed

42 A patient-pathway analysis (PPA) was completed to assess the alignment between patie

43 A patient-pathway analysis (PPA) was conducted at the national level, as well as for

44 A patient pathway analysis (PPA) was conducted to assess the alignment between patie

45 Following discrepant analysis, PPA and NPA values were as follows: 97.3% and 99.8% for

46 tudy of disease genes identified in 2012 and PPA data produced before that date.

47 ncremental utility at low DB levels (CBS and PPA) and were associated with overlapping and distinct n

48 odalities were useful in identifying CBS and PPA, whereas DB alone was useful for identifying bvFTD.

49 emental changes in the topography of FFA and PPA (predicted by the continuous-mapping model) or (ii)

50 magnitude of baseline shifts in the FFA and PPA across subjects.

51 asure the activation elicited in the FFA and PPA by each of 96 object images from a wide range of cat

52 Results suggest that responses in FFA and PPA exhibit almost perfect categorical ranking, are grad

53 tions with specialized areas such as FFA and PPA.

54 f human regions fusiform face area (FFA) and PPA (which are adjacent to each other in cortex), the pr

55 displacement experiments showed that OPA and PPA were the predominant surface-bound ligands.

56 Human RSC and PPA are located adjacent to the peripheral representatio

57 ; 95% confidence interval, significance) and PPA progression (1.7; 1.2-2.4, P = .002).

58 nd for T2, increases were seen at the SZ and PPA only.

59 mentia (bvFTD), primary progressive aphasia (PPA) and corticobasal syndrome (CBS).

60 tia syndrome of primary progressive aphasia (PPA) can be caused by 1 of several neuropathologic entit

61 Primary progressive aphasia (PPA) is a clinical dementia syndrome characterized by pr

62 Primary progressive aphasia (PPA) is a clinical syndrome characterised by progressive

63 Primary progressive aphasia (PPA) is a neurodegenerative dementia syndrome principall

64 Primary progressive aphasia (PPA) is a neurodegenerative syndrome that causes a gradu

65 Primary progressive aphasia (PPA) is a progressive language disorder associated with

66 stimulation in primary progressive aphasia (PPA) is a promising approach.

67 ntic variant of primary progressive aphasia (PPA) is characterized by the combination of word compreh

68 Primary progressive aphasia (PPA) refers to a disorder of declining language associat

69 f patients with primary progressive aphasia (PPA) variants defined by current diagnostic classificati

70 Primary progressive aphasia (PPA), a selective neurodegeneration of the language netw

71 f patients with primary progressive aphasia (PPA), but clinical features that predict AD pathology in

72 uent variant of primary progressive aphasia (PPA), degeneration of the posterior IFC is associated wi

73 In primary progressive aphasia (PPA), speech and language difficulties are caused by neu

74 f deposition in primary progressive aphasia (PPA).

75 or faces) to the parahippocampal place area (PPA) (apparently selective for places), testing for (i)

76 ific ROIs in the parahippocampal place area (PPA) and posterior collateral sulcus.

77 tenuation in the parahippocampal place area (PPA) and retrosplenial cortex (RSC), but no such extrapo

78 ry manner by the parahippocampal place area (PPA) and the lateral occipital complex (LOC) in particul

79 ctivation of the parahippocampal place area (PPA) and the retrosplenial cortex (RSC) for visual and h

80 al connection to parahippocampal place area (PPA) compared with adjacent regions (e.g., fusiform face

81 ventral temporal parahippocampal place area (PPA) has been implicated in scene processing, but scene

82 For example, the parahippocampal place area (PPA) responds maximally to environmental scenes during f

83 o words, and the parahippocampal place area (PPA) showed effects for recall vs. familiarity specific

84 e area (FFA) and parahippocampal place area (PPA) was modulated such that activity was higher during

85 we show that the parahippocampal place area (PPA), a region in human occipitotemporal cortex, exhibit

86 sual cortex, the parahippocampal place area (PPA), and the retrosplenial cortex (RSC).

87 patterns in the parahippocampal place area (PPA), even though this region responds strongly to scene

88 e area (FFA) and parahippocampal place area (PPA), respectively.

89 patterns in the parahippocampal place area (PPA), retrosplenial complex (RSC), and occipital place a

90 hat area V1, the parahippocampal place area (PPA), retrosplenial cortex (RSC), and lateral occipital

91 processing: the parahippocampal place area (PPA), the retrosplenial complex (RSC), and a region arou

92 sual cortex [the parahippocampal place area (PPA), transverse occipital sulcus (TOS), and retrospleni

93 responses in the parahippocampal place area (PPA), transverse occipital sulcus, and retrosplenial cor

94 s region and the parahippocampal place area (PPA), which previous studies indicate play a critical ro

95 s, including the parahippocampal place area (PPA).

96 ea (FFA) and the parahippocampal place area (PPA).

97 verlaps with the parahippocampal place area (PPA).

98 response within parahippocampal place area (PPA).

99 ubpistonal area [SPA] and peripistonal area [PPA]) were defined as regions of interest.

100 This area (the parahippocampal place area [PPA]) was initially interpreted as responding selectivel

101 S)- and place ('parahippocampal place area', PPA)-selective cortices in children (ages 7-11), adolesc

102 rtical area (the parahippocampal place area; PPA) showed distinctively higher functional magnetic res

103 s with posterior probability of association (PPA) greater than 0.5 in the discovery cohort.

104 ere, we analyze protein-protein association (PPA) networks to identify candidate genes in the vicinit

105 ession (kappa = 0.7), parapapillary atrophy (PPA) progression (kappa = 0.7), disc hemorrhages (kappa

106 d for the presence of peripapillary atrophy (PPA), peripapillary pigment (PPP), drusen in the macula,

107 y (DOT) using preprescription authorization (PPA) vs postprescription review with feedback (PPRF) str

108 h individual scenes could be decoded in both PPA and early visual cortex (EVC), the structure of repr

109 FDG patterns were focal and varied by PPA subtype, with left temporoparietal hypometabolism in

110 verall, these results indicate that chitosan-PPA beads show potential for lower gastrointestinal deli

111 entrapment of the proteins in these chitosan-PPA beads.

112 The helical cis-PPA backbone undergoes reversible extension and contract

113 soid conformational isomerization of the cis-PPA.

114 the self-organizable dendronized helical cis-PPAs form oriented bundles.

115 ed cis-transoidal polyphenylacetylenes ( cis-PPAs) that possess a first-order phase transition from a

116 Among patients with clinical PPA syndrome, AD neuropathology appeared to interfere wi

117 uasi-experimental, crossover trial comparing PPA and PPRF for adult inpatients prescribed any antibio

118 neuropathological analyses of 23 consecutive PPA autopsies.

119 Current PPA criteria divide PPA into three variants: non-fluent

120 iated by boron trifluoride results in cyclic PPA in high yield, with high molecular weight, and with

121 end groups enhances the stability of cyclic PPA and makes it an attractive candidate for lithographi

122 ing to PPA's low ceiling temperature, cyclic PPA is capable of chain extension to larger molecular we

123 In contrast, the differential PPA response to buildings versus nonbuildings occurred l

124 Poly(phosphoramidate-dipropylamine) (PPA) and Lipid-Protamine-DNA (LPD) nanoparticles consist

125 the single MR modality models to distinguish PPA variants (accuracy was 0.86, 0.73, and 0.68 for the

126 Current PPA criteria divide PPA into three variants: non-fluent (nfvPPA), semantic (

127 Although each PPA subtype is characterized by the nature of the princi

128 INTERPRETATION: Each PPA clinical variant is associated with a typical and mo

129 A subset of AspAT Ib enzymes exhibiting PPA-AT activity was further identified from both Plantae

130 imply a causal role in scene processing for PPA and RSC, no such evidence exists for OPA.

131 vFTD from CBS patients and 93% of bvFTD from PPA patients-30% and 13% above base rates (59%, 80%), re

132 egorization performance and predictions from PPA exhibited a significant decrease in accuracy when sc

133 either AD (PPA-AD) or a tau variant of FTLD (PPA-FTLD) and 6 patients who had the clinical diagnosis

134 over number (4371), activity (1.05 x 10(6) g(PPA) mol(cat)(-1) h(-1)),and yield (87%) for the polymer

135 characterization, the PLEX-ID Flu assay had PPAs and NPAs of 98.3% and 97.5% for H1N1-p, 88.6% and 1

136 ex), the presumptive monkey homolog of human PPA is located adjacent to the monkey homolog of human F

137 hat the AD markers encountered at autopsy in PPA may not always reflect the nature of the initiating

138 that contribute to object naming failures in PPA.

139 However, in PPA, representations were defined primarily by the spati

140 asymmetric (favoring left hypometabolism) in PPA (p < 0.005) but not in AD.

141 A 10% increase in PPA was associated with a 24% (p < 0.0003) decrease in t

142 lateralized pattern of neurodegeneration in PPA.

143 nd has rarely been performed in health or in PPA.

144 the preference for cardinal orientations in PPA, thus demonstrating that the oblique effect can also

145 inical features that predict AD pathology in PPA are not well defined.

146 typical AD, did not predict AD pathology in PPA.

147 Language phenotype in PPA is closely related to metabolic changes that are foc

148 t the oblique effect can also be produced in PPA by simple geometrical images, with statistics simila

149 FA; the category step was more pronounced in PPA.

150 Even more remarkably, in PPA and RSC, error patterns for decoding from line drawi

151 correlated strongly with representations in PPA and peripheral EVC, respectively.

152 ng block for category-selective responses in PPA and functionally related areas.

153 o the emergence of language deficits seen in PPA.

154 at the endocytosed, quantum dot (QD)-labeled PPA-DNA nanoparticles remained in the intestinal cells e

155 bjects and increases BOLD signal in the left PPA when viewing scenes.

156 Simulated successional patterns by LM3-PPA from the leaf physiological trade-offs are consisten

157 al-based dynamic vegetation model (i.e., LM3-PPA).

158 rly individuals living in nursing homes, low PPA from central to peripheral arteries strongly predict

159 , in both SGF and SIF, was achieved with low PPA concentration.

160 Patients meeting PPA criteria (N = 15) were classified as logopenic aphas

161 (nfvPPA), 11 logopenic (lvPPA), and 4 mixed PPA.

162 unctional status of this region in nonfluent PPA is not well understood.

163 In nonfluent PPA patients, the posterior IFC was atrophic and, unlike

164 We conclude that in nonfluent PPA, the posterior IFC is not only structurally damaged,

165 syntactically complex sentences in nonfluent PPA.

166 ension task in eight patients with nonfluent PPA, compared to healthy age-matched controls.

167 this review, I discuss linguistic aspects of PPA syndromes that may prove informative for parsing our

168 ing and memory in autopsy-confirmed cases of PPA.

169 The classification of PPA into one of the three variants may be performed at 3

170 ts who had the primary clinical diagnosis of PPA and an autopsy-confirmed diagnosis of either AD (PPA

171 Imaging-supported diagnosis of PPA variant is more feasible with quantitative analysis

172 A clinical diagnosis of PPA was associated with frontotemporal lobar degeneratio

173 lity of the imaging-supported diagnostics of PPA variants in the Polish clinical setting with access

174 , the subtle learning and memory features of PPA and their neuropathologic associations have not been

175 ly logopenic, agrammatic, and mixed forms of PPA.

176 A second group of PPA patients showed more severe naming deficits-the obje

177 were more numerous in the left hemisphere of PPA/AD.

178 ng (SPECT, albeit not MRI), thus level II of PPA diagnosis could be established in those cases.

179 Furthermore, the response of PPA could not be used to decode the high-level semantic

180 idosis, suggesting that subclassification of PPA based on language features can help predict the like

181 les described in any of the sub-syndromes of PPA.

182 Although early theories of PPA emphasized its role in spatial processing, more rece

183 de of TEER decrease and halved the uptake of PPA-DNA nanoparticles.

184 country case studies that profile the use of PPA.

185 Variants of PPA are important to recognize from a medical perspectiv

186 Two series of PPAs substituted at the phenyl ring in ortho, meta, and

187 t of candidates together with information on PPAs, frequency and predicted pathogenicity of the varia

188 The optimized PPA/P2 O5 medium is a mild acid that is not only less co

189 ve region (the parahippocampal place area or PPA) was tolerant to mirror reversals.

190 ior frontal junction, IFJ, and either FFA or PPA, depending on which object was attended.

191 advanced by 20 ms in IFJ compared to FFA or PPA.

192 , which were not observed in the PPA-FTLD or PPA-AD groups (all P < .005).

193 ulty with centre-embedded sentences in other PPA variants was related to other brain regions.

194 End-capped poly(phthalaldehyde) (PPA) synthesized by anionic polymerization has garnered

195 Plant PPA-ATs and succeeding arogenate dehydratases (ADTs) wer

196 In PIB-positive PPA, PIB uptake was diffuse and indistinguishable from t

197 alternative ionic polymerizations to produce PPA have been largely unexplored.

198 There are three recognized PPA variants: agrammatic, semantic, and logopenic.

199 ontrary to recent reports, that the response PPA primarily reflects spatial, not categorical or conte

200 observed in helical poly(phenylacetylene)s (PPAs) when either the type of linkage with the pendant g

201 t current stimulation (tDCS) on the semantic PPA variant (sv-PPA), applying a rigorous study design t

202 ure, which occurs within the scene-sensitive PPA, is a route to accessing knowledge about an object's

203 Syphilis IgG immunoassay displayed a similar PPA (100%) but a substantially lower NPA (15.9%).

204 ith ADT, a gene encoding prephenate-specific PPA-AT was transferred from a Chlorobi/Bacteroidetes anc

205 ere collected from 69 patients with sporadic PPA, divided into 29 semantic (svPPA), 25 nonfluent (nfv

206 gional effective connectivity in early-stage PPA (n = 8) and control (n = 8) subjects performing sema

207 In a previous functional neuroimaging study, PPA patients were found to activate core language areas

208 For its part, the ortho-substituted PPA (o-poly-1) presents a highly stretched, almost plana

209 Meta-substituted PPAs (m-poly-1 and m-poly-2) exist as a mixture in equil

210 Subtyping PPA helps to predict AD versus frontotemporal lobar dege

211 itions targeting the temporal poles of 12 sv-PPA patients.

212 rous study design to a large, homogeneous sv-PPA cohort.

213 predominantly left-lateralized damage in sv-PPA and accounts of interhemispheric inhibition, we appl

214 ngs demonstrate the efficiency of tDCS in sv-PPA by generating highly specific intrasemantic effects.

215 ation (tDCS) on the semantic PPA variant (sv-PPA), applying a rigorous study design to a large, homog

216 The Chlorobium tepidum PPA-AT and ADT homologs indeed efficiently converted pre

217 We found that PPA was consistently activated by rectilinear features,

218 Here, we hypothesized that PPA responds selectively to a lower-level stimulus prope

219 We hypothesized that PPA responses to scenes and buildings might be driven by

220 However, subsequent studies reported that PPA also responds strongly to a much wider range of imag

221 These results show that PPA reflects a selective disruption of the language netw

222 sequent displacement experiments showed that PPA was the predominant surface-bound ligand.

223 The PPA assessed the alignment between patient care seeking

224 The PPA can help programs understand where they might find t

225 The PPA for identification of resistance determinants was as

226 The PPA identified opportunities for strengthening access to

227 The PPA results emphasize the role that the private sector p

228 The PPA results revealed that only 20% of patients encounter

229 The PPA was a predictor of total mortality and major CV even

230 The PPA was shown to form during the nanoparticle synthesis

231 The PPA-FTLD (n = 6), PPA-AD (n = 7), and AMN-AD (n = 6) gro

232 The PPA-FTLD group had normal (ie, near-ceiling) scores on a

233 The PPA/AD group showed predominance of entorhinal NFT typic

234 pectrum of functional groups accessible, the PPA/P2 O5 -driven Friedel-Crafts acylation offers more o

235 rovide further evidence that V1, RSC and the PPA not only contain information relevant for natural sc

236 ddition to effects of category in LO and the PPA.

237 regions of human visual cortex, such as the PPA, has been linked to the semantic and categorical pro

238 We discover that, whereas both the PPA and LOC can accurately classify scenes, they make di

239 Both the PPA-AD and AMN-AD groups had deficits in verbal effortle

240 Discussion: The PPA can be a valuable planning and programming tool to e

241 Discussion: The PPA results emphasized the need for a differentiated app

242 sify scenes, they make different errors: the PPA more often confuses scenes that have the same spatia

243 Taken together, these findings establish the PPA/RSC network as critical in modality-independent spat

244 Median patient DOTs in the PPA and PPRF arms were 8 and 6 DOT per 1000 PD, respecti

245 ic DOTs remained relatively unchanged in the PPA arm.

246 nowing the correspondences among them in the PPA but not in the other two regions, suggesting that th

247 neural response to different clusters in the PPA could be predicted by the similarity in their image

248 % and 41% of patients on days 1 and 3 in the PPA group (P < .01) and in 57% and 36% of patients on da

249 eater left lateralized amyloid uptake in the PPA group than the amnestic group (p < 0.007), consisten

250 between Wernicke's and Broca's areas in the PPA patient group.

251 Interestingly, the neural response in the PPA was also predicted by perceptual responses to the sc

252 accuracy for good than bad exemplars in the PPA, RSC and V1.

253 suggest that the information present in the PPA, RSC, and LOC is likely to contribute to natural sce

254 effect of familiarity in RSC but not in the PPA, with the former region responding much more strongl

255 8.33 [5.2]), which were not observed in the PPA-FTLD or PPA-AD groups (all P < .005).

256 processing of global scene properties in the PPA.

257 distinct patterns of neural response in the PPA.

258 est that a network of regions, including the PPA, RSC, and LOC, contribute to the human ability to ca

259 d the observation that lesions involving the PPA cause topographic disorientation, there is little ca

260 Our results support the causal role of the PPA in the perception of visual scenes, demonstrate that

261 levant for the differential diagnosis of the PPA variants in clinical practice.

262 itional quantitation was done in four of the PPA/AD cases and four AD cases with the typical amnestic

263 Specifically, the PPA treats different perceptual instantiations of the sa

264 These results suggest that the PPA and RSC play distinct but complementary roles in pla

265 We found that the PPA distinguished scene from nonscene stimuli in approxi

266 t finding challenges the hypothesis that the PPA is involved in navigation and reorientation and sugg

267 n the other two regions, suggesting that the PPA is the key region involved in learning the different

268 were 2686 and 2693 patients admitted to the PPA and PPRF groups, with 29% and 27% of patients prescr

269 onths, 2 medicine teams were assigned to the PPA arm and the other 2 teams to the PPRF arm.

270 D) but remained constant when changed to the PPA arm.

271 o scenes compared with faces, similar to the PPA.

272 Whereas the PPA was impervious to task modulation, responses from tw

273 f the linguistic variables compared with the PPA variants showed that a third of patients had normal

274 This analysis aggregates and compares the PPAs from case studies in Kenya, Ethiopia, Indonesia, th

275 amyloidosis, and glucose metabolism in three PPA variants using [11C]-Pittsburgh compound B ([11C]PIB

276 hotographs, in primary visual cortex through PPA and RSC.

277 Thus, PPA shows distinctive fMRI selectivity for cardinal orie

278 ofile and an atypical functional coupling to PPA compared with human controls.

279 Owing to PPA's low ceiling temperature, cyclic PPA is capable of

280 at the best markers to differentiate the two PPA variants at an individual patient level among cortic

281 a discussion of nonfluent/agrammatic variant PPA, the supporting role of short-term memory in a discu

282 al variant FTD (bvFTD), 7 non-fluent variant PPA (nfvPPA), 6 semantic variant PPA (svPPA) and 25 pati

283 memory in a discussion of logopenic variant PPA, and components of language associated with discours

284 ent variant PPA (nfvPPA), 6 semantic variant PPA (svPPA) and 25 patients with subjective cognitive im

285 meaning in a discussion of semantic variant PPA, grammatical comprehension and expression in a discu

286 SPA versus PPA changes were significant at the SZ and TZ (T1), TZ a

287 ges in the entire sample depth of SPA versus PPA were found for delta1/2 (T1rho, 14% +/- 12 vs 6% +/-

288 rval [CI]: 1.01 to 1.14; p = 0.016), whereas PPA independently predicted all CVEs (HR per 10% increas

289 gest a tripartite division of labor, whereby PPA codes landmark identity, RSC retrieves spatial or co

290 Then we tested whether PPA is selectively activated by rectangular features in

291 on decreasing antibiotic DOTs compared with PPA.

292 s (4 women, 2 men) clinically diagnosed with PPA (3 with nfvPPA and 3 with lvPPA) in whom MRI and SPE

293 increased tight junction permeability, with PPA and PEI having the most dramatic transepithelial ele

294 In 33 human subjects with PPA, object naming and word comprehension were explored

295 tional IA risk loci, we pursued 14 loci with PPAs in the discovery cohort between 0.1 and 0.5.

296 owed reduced scene-selective activity within PPA compared with healthy matched controls.

297 duces the level of selective activity within PPA, which may lead to related perceptual impairments in

298 he generation of "selective" activity within PPA.

299 f VCSL disruption on neural processes within PPA, HD patients showed reduced scene-selective activity

300 Disc, alpha-zone, and beta-zone PPA were traced independently by 2 trained readers and t