ライフサイエンスコーパス: PPA

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

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

3 verlaps with the parahippocampal place area (PPA).

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

5 response within parahippocampal place area (PPA).

6 f deposition in primary progressive aphasia (PPA).

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

8 tions with specialized areas such as FFA and PPA.

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

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

11 on decreasing antibiotic DOTs compared with PPA.

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

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

14 processing of global scene properties in the PPA.

15 distinct patterns of neural response in the PPA.

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

17 country case studies that profile the use of PPA.

18 syntactically complex sentences in nonfluent PPA.

19 that contribute to object naming failures in PPA.

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

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

22 lateralized pattern of neurodegeneration in PPA.

23 he generation of "selective" activity within PPA.

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

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

26 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

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

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

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

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

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

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

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

34 The PPAD active site is a funnel located on one of the cylin

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

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

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

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

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

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

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

42 re tightly bound, which explains activity of PPAD against arginines at C-termini but not within pepti

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

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

45 te Snail family proteins, Partner of paired (Ppa), also controlled Twist stability and did so in a ma

46 One of these is peptidylarginine deiminase (PPAD), an enzyme unique to P. gingivalis among bacteria,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 Here, we studied function of PPAD and its substrate-free, substrate-complex, and subs

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

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

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

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

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

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

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

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

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

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

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

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

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

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

81 Expression of PAD2 and PAD4, PPAD, and citrullinated proteins were assessed by either

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

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

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

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

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

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

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

89 ic DOTs remained relatively unchanged in the PPA arm.

90 The PPA assessed the alignment between patient care seeking

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

109 monas gingivalis peptidylarginine deiminase (PPAD) can influence citrullination of proteins by either

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

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

112 Here, we report that PPAD citrullination of a critical C-terminal arginine of

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

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

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

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

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

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

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

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

121 Our results provide an example of how pPA contributes to cancer by generating a truncated mRNA

122 Surprisingly, Ppa could also target the third core EMT regulatory fact

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

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

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

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

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

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

129 A PPA describes the steps that people with tuberculosis ta

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

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

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

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

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

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

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

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

138 We identify a pPA event at a cryptic intronic poly(A) signal in MAGI3,

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

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

141 arthritis development in mice infected with PPAD-expressing P. gingivalis, our findings support a cr

142 asmic ubiquitin-ligases beta-TrCP1/FBXW1 and Ppa/FBXL14.

143 The PPA for identification of resistance determinants was as

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

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

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

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

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

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

150 8.33 [5.2]), which were not observed in the PPA-FTLD or PPA-AD groups (all P < .005).

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

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

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

154 % and 41% of patients on days 1 and 3 in the PPA group (P < .01) and in 57% and 36% of patients on da

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

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

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

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

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

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

161 The PPA identified opportunities for strengthening access to

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

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

164 alis, our findings support a crucial role of PPAD in the virulence of P. gingivalis.

165 Treatment of C5a with PPAD in vitro resulted in decreased chemotaxis of human

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

167 d evidence for recurrent expression of MAGI3(pPA) in primary human breast tumors but not in tumor-adj

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

195 native C5a was detected after treatment with PPAD-null outer membrane vesicles.

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

197 Ppa-obi-1 encodes lipid-binding domains and reaches its

198 mone sensitivity, a newly identified mutant, Ppa-obi-1, is used to reveal the molecular links between

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

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

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

202 hich premature cleavage and polyadenylation (pPA) of RNA can produce an oncogenic protein.

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

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

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

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

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

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

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

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

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

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

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

214 comparative study of six (D, Vd, Vv, Dm, Dl, Ppa) periventricular zones (PVZs) harboring proliferativ

215 n the sequences of eight housekeeping genes (ppa, pgm, gyrB, gmk, glyA, atpA, arcC, and adk) and appl

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

217 crobes, P. gingivalis secretes a PAD, termed PPAD (Porphyromonas peptidylarginine deiminase), which i

218 and Vl, respectively]), as well as preoptic (PPa, PPp, and PM), pretectal (PPd, PPv, PCN, PSp, and PS

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

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

221 The altered mRNA isoform, called MAGI3(pPA), produces a truncated protein that acts in a domina

222 ; 95% confidence interval, significance) and PPA progression (1.7; 1.2-2.4, P = .002).

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

224 PPA provides a novel perspective that uniquely addresses

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

246 Thus, PPA shows distinctive fMRI selectivity for cardinal orie

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

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

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

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

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

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

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

254 ase (Pdi), a UDP-hydrolase (Phy), an enzyme (Ppa) that adds phosphoenolpyruvate to form pseudaminic a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

282 The PPA was shown to form during the nanoparticle synthesis

283 rullination of internal arginine residues by PPAD was also detected using mass spectrometry.

284 PPAD was detected only in mononuclear cells incubated in

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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