human | Q5 |
P2456 | DBLP author ID | 65/7224 |
P8446 | Gateway to Research person ID | 70C08E23-5312-490A-AE06-3F7D93940799 |
P227 | GND ID | 1020893028 |
P8189 | National Library of Israel J9U ID | 987009748103505171 |
P856 | official website | http://www.mrc-cbu.cam.ac.uk/people/matt.lambon-ralph/ |
P496 | ORCID iD | 0000-0001-5907-2488 |
P3829 | Publons author ID | 2877851 |
P1053 | ResearcherID | A-1695-2009 |
P1153 | Scopus author ID | 7003333514 |
P214 | VIAF ID | 233408400 |
P166 | award received | Charles Darwin Award Lecture | Q59282490 |
P735 | given name | Matthew | Q4927231 |
Matthew | Q4927231 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | male | Q6581097 |
Q28749293 | "Pre-semantic" cognition revisited: critical differences between semantic aphasia and semantic dementia |
Q59297696 | "Presemantic" Cognition in Semantic Dementia: Six Deficits in Search of an Explanation |
Q38408972 | "Presemantic" cognition in semantic dementia: six deficits in search of an explanation. |
Q59297685 | A Case Series Comparison to Investigate the Comprehension Impairment in Wernicke's Aphasia |
Q60530521 | A Distinctive Case of Word Meaning Deafness? |
Q38424341 | A category-specific advantage for numbers in verbal short-term memory: evidence from semantic dementia |
Q58264573 | A comparison of word versus sentence cues as therapy for verb naming in aphasia |
Q38475339 | A direct comparison of errorless and errorful therapy for object name relearning in Alzheimer's disease |
Q38430777 | A duck with four legs: Investigating the structure of conceptual knowledge using picture drawing in semantic dementia |
Q38836208 | A graded tractographic parcellation of the temporal lobe. |
Q114633298 | A middle ground where executive control meets semantics: the neural substrates of semantic control are topographically sandwiched between the multiple-demand and default-mode systems |
Q38416943 | A semantic contribution to nonword recall? Evidence for intact phonological processes in semantic dementia |
Q92389570 | A structural connectivity convergence zone in the ventral and anterior temporal lobes: Data-driven evidence from structural imaging |
Q97516978 | A tutorial and tool for exploring feature similarity gradients with MRI data |
Q42289644 | A unified model of human semantic knowledge and its disorders |
Q93209861 | A unified model of post-stroke language deficits including discourse production and their neural correlates |
Q95660344 | A unified neurocognitive model of semantics language social behaviour and face recognition in semantic dementia |
Q104063814 | A unified neurocomputational bilateral model of spoken language production in healthy participants and recovery in poststroke aphasia |
Q59297694 | Acquired Disorders of Reading |
Q59297697 | Age of acquisition effects depend on the mapping between representations and the frequency of occurrence: Empirical and computational evidence |
Q38376758 | Amodal semantic representations depend on both anterior temporal lobes: evidence from repetitive transcranial magnetic stimulation |
Q58263635 | An emergent effect of phonemic cueing following relearning in semantic dementia |
Q38377949 | An emergent functional parcellation of the temporal cortex |
Q58142816 | Anomia is simply a reflection of semantic and phonological impairments: Evidence from a case-series study |
Q30484639 | Anterior temporal lobe connectivity correlates with functional outcome after aphasic stroke |
Q36289103 | Anterior temporal lobes mediate semantic representation: mimicking semantic dementia by using rTMS in normal participants |
Q37908394 | Arcuate fasciculus variability and repetition: the left sometimes can be right |
Q33825049 | Arterial spin labelling shows functional depression of non-lesion tissue in chronic Wernicke's aphasia |
Q90025698 | Assessing and mapping language, attention and executive multidimensional deficits in stroke aphasia |
Q38497170 | At the edge of semantic space: the breakdown of coherent concepts in semantic dementia is constrained by typicality and severity but not modality |
Q59297703 | Automatic and controlled processing in sentence recall: The role of long-term and working memory |
Q38469192 | Be concrete to be comprehended: consistent imageability effects in semantic dementia for nouns, verbs, synonyms and associates |
Q96137907 | Bipartite Functional Fractionation within the Default Network Supports Disparate Forms of Internally Oriented Cognition |
Q38471063 | Both the middle temporal gyrus and the ventral anterior temporal area are crucial for multimodal semantic processing: distortion-corrected fMRI evidence for a double gradient of information convergence in the temporal lobes |
Q30425468 | Capturing multidimensionality in stroke aphasia: mapping principal behavioural components to neural structures |
Q58170284 | Case series, neuroscience-infused, computational neuropsychology will play a crucial role in the future of aphasiology. Commentary on Laine and Martin, “Cognitive neuropsychology has been, is, and will be significant to aphasiology” |
Q33885639 | Category-specific versus category-general semantic impairment induced by transcranial magnetic stimulation |
Q59297678 | Clarification of conclusions from the ACT NoW trial |
Q46495053 | Clinical effectiveness, cost-effectiveness and service users' perceptions of early, well-resourced communication therapy following a stroke: a randomised controlled trial (the ACT NoW Study). |
Q59297676 | Cognitive neuroscience of aphasia recovery and therapy |
Q33664597 | Coherent concepts are computed in the anterior temporal lobes |
Q33568813 | Comprehension of concrete and abstract words in semantic dementia |
Q55279546 | Concepts, control, and context: A connectionist account of normal and disordered semantic cognition. |
Q36499580 | Conceptual Structure within and between Modalities |
Q38388287 | Conceptual knowledge is underpinned by the temporal pole bilaterally: convergent evidence from rTMS. |
Q55500501 | Concrete versus abstract forms of social concept: an fMRI comparison of knowledge about people versus social terms. |
Q90784180 | Connectivity Gradient in the Human Left Inferior Frontal Gyrus: Intraoperative Cortico-Cortical Evoked Potential Study |
Q38041104 | Connectivity-based structural and functional parcellation of the human cortex using diffusion imaging and tractography |
Q92444923 | Control the source: Source memory for semantic, spatial and self-related items in patients with LIFG lesions |
Q55240567 | Controlled semantic cognition relies upon dynamic and flexible interactions between the executive 'semantic control' and hub-and-spoke 'semantic representation' systems. |
Q38469222 | Convergent connectivity and graded specialization in the rostral human temporal lobe as revealed by diffusion-weighted imaging probabilistic tractography. |
Q47643156 | Cued Memory Reactivation During SWS Abolishes the Beneficial Effect of Sleep on Abstraction |
Q38440795 | Deficits in irregular past-tense verb morphology associated with degraded semantic knowledge. |
Q36596970 | Deficits of knowledge versus executive control in semantic cognition: insights from cued naming |
Q38471768 | Deficits of semantic control produce absent or reverse frequency effects in comprehension: evidence from neuropsychology and dual task methodology |
Q48316480 | Demonstrating a wordlikeness effect on nonword repetition performance in a conduction aphasic patient |
Q38469368 | Demonstrating the qualitative differences between semantic aphasia and semantic dementia: a novel exploration of nonverbal semantic processing. |
Q38428708 | Deregulated semantic cognition contributes to object-use deficits in Alzheimer's disease: A comparison with semantic aphasia and semantic dementia |
Q38500463 | Deregulated semantic cognition follows prefrontal and temporo-parietal damage: evidence from the impact of task constraint on nonverbal object use. |
Q37397127 | Different impairments of semantic cognition in semantic dementia and semantic aphasia: evidence from the non-verbal domain |
Q38495964 | Different roles of lateral anterior temporal lobe and inferior parietal lobule in coding function and manipulation tool knowledge: evidence from an rTMS study |
Q38493546 | Differential contributions of bilateral ventral anterior temporal lobe and left anterior superior temporal gyrus to semantic processes. |
Q35049489 | Differing contributions of inferior prefrontal and anterior temporal cortex to concrete and abstract conceptual knowledge |
Q30402244 | Direct Exploration of the Role of the Ventral Anterior Temporal Lobe in Semantic Memory: Cortical Stimulation and Local Field Potential Evidence From Subdural Grid Electrodes |
Q36092458 | Disorders of representation and control in semantic cognition: Effects of familiarity, typicality, and specificity. |
Q34279793 | Dissecting the function of networks underpinning language repetition |
Q38411326 | Dissociating reading processes on the basis of neuronal interactions |
Q35681080 | Dissociating stimulus-driven semantic and phonological effect during reading and naming |
Q38399840 | Distinct patterns of olfactory impairment in Alzheimer's disease, semantic dementia, frontotemporal dementia, and corticobasal degeneration |
Q48314588 | Distortion correction for diffusion-weighted MRI tractography and fMRI in the temporal lobes |
Q30829297 | Do You Read How I Read? Systematic Individual Differences in Semantic Reliance amongst Normal Readers |
Q35847245 | Do deep dyslexia, dysphasia and dysgraphia share a common phonological impairment? |
Q58302720 | Domain-specific control of semantic cognition: A dissociation within patients with semantic working memory deficits |
Q36094074 | Effectiveness of enhanced communication therapy in the first four months after stroke for aphasia and dysarthria: a randomised controlled trial |
Q34295994 | Efficient visual object and word recognition relies on high spatial frequency coding in the left posterior fusiform gyrus: evidence from a case-series of patients with ventral occipito-temporal cortex damage |
Q38380423 | Elucidating the nature of deregulated semantic cognition in semantic aphasia: evidence for the roles of prefrontal and temporo-parietal cortices |
Q58142821 | Errorless and errorful therapy for verb and noun naming in aphasia |
Q50964413 | Errorless learning and rehabilitation of language and memory impairments. |
Q35796127 | Establishing task- and modality-dependent dissociations between the semantic and default mode networks. |
Q91014787 | Establishing the cognitive signature of human brain networks derived from structural and functional connectivity |
Q104616883 | Establishing two principal dimensions of cognitive variation in logopenic progressive aphasia |
Q99585541 | Evaluating the granularity and statistical structure of lesions and behaviour in post-stroke aphasia |
Q36524942 | Executive semantic processing is underpinned by a large-scale neural network: revealing the contribution of left prefrontal, posterior temporal, and parietal cortex to controlled retrieval and selection using TMS. |
Q38496257 | Explaining semantic short-term memory deficits: evidence for the critical role of semantic control |
Q64090738 | Exploring distinct default mode and semantic networks using a systematic ICA approach |
Q37509340 | Exploring multimodal semantic control impairments in semantic aphasia: evidence from naturalistic object use. |
Q52048992 | Exploring the impact of plasticity-related recovery after brain damage in a connectionist model of single-word reading. |
Q59297680 | Facilitating and disrupting speech perception in word deafness |
Q39594130 | Finite case series or infinite single-case studies? Comments on "Case series investigations in cognitive neuropsychology" by Schwartz and Dell (2010). |
Q51767660 | From percept to concept in the ventral temporal lobes: Graded hemispheric specialisation based on stimulus and task. |
Q38375031 | Frontotemporal lobar degeneration and social behaviour: Dissociation between the knowledge of its consequences and its conceptual meaning |
Q48193652 | Fundamental deficits of auditory perception in Wernicke's aphasia |
Q58259291 | Further explorations and an overview of errorless and errorful therapy for aphasic word-finding difficulties: The number of naming attempts during therapy affects outcome |
Q30402255 | Fusion and Fission of Cognitive Functions in the Human Parietal Cortex |
Q47161263 | GABA concentrations in the anterior temporal lobe predict human semantic processing |
Q37133694 | Generalization and differentiation in semantic memory: insights from semantic dementia |
Q38448327 | Going beyond inferior prefrontal involvement in semantic control: evidence for the additional contribution of dorsal angular gyrus and posterior middle temporal cortex |
Q26778911 | Graded specialization within and between the anterior temporal lobes |
Q99560530 | Graded, multidimensional intra- and intergroup variations in primary progressive aphasia and post-stroke aphasia |
Q48492510 | Guilt-selective functional disconnection of anterior temporal and subgenual cortices in major depressive disorder |
Q38400593 | Hemispheric Specialization within the Superior Anterior Temporal Cortex for Social and Nonsocial Concepts |
Q38427228 | Homogeneity and heterogeneity in mild cognitive impairment and Alzheimer's disease: a cross-sectional and longitudinal study of 55 cases |
Q58140961 | How does linguistic knowledge contribute to short-term memory? Contrasting effects of impaired semantic knowledge and executive control |
Q51892767 | How intensive does anomia therapy for people with aphasia need to be? |
Q59297687 | How many words should we provide in anomia therapy? A meta-analysis and a case series study |
Q38423520 | Implicit recognition in pure alexia: The Saffran effect-a tale of two systems or two procedures? |
Q38376724 | Induction of semantic impairments using rTMS: evidence for the hub-and-spoke semantic theory. |
Q92095574 | Investigating the effect of changing parameters when building prediction models for post-stroke aphasia |
Q59297674 | Investigating the language, cognition and self-monitoring abilities of speakers with jargon output |
Q112684633 | Joint recording of EEG and audio signals in hyperscanning and pseudo-hyperscanning experiments |
Q112580365 | Language Disorder in Progressive Supranuclear Palsy and Corticobasal Syndrome: Neural Correlates and Detection by the MLSE Screening Tool |
Q49146798 | Lateralization of ventral and dorsal auditory-language pathways in the human brain. |
Q59297699 | Lexical and semantic binding in verbal short-term memory |
Q38407855 | Lexical and semantic influences on item and order memory in immediate serial recognition: evidence from a novel task |
Q43489590 | Lichtheim 2: synthesizing aphasia and the neural basis of language in a neurocomputational model of the dual dorsal-ventral language pathways |
Q48716175 | Listening to narrative speech after aphasic stroke: the role of the left anterior temporal lobe |
Q34094559 | Longitudinal profiles of semantic impairment for living and nonliving concepts in dementia of Alzheimer's type. |
Q33365355 | Mapping Domain-Selective and Counterpointed Domain-General Higher Cognitive Functions in the Lateral Parietal Cortex: Evidence from fMRI Comparisons of Difficulty-Varying Semantic Versus Visuo-Spatial Tasks, and Functional Connectivity Analyses |
Q92774128 | Mapping psycholinguistic features to the neuropsychological and lesion profiles in aphasia |
Q38391958 | Mapping the Dynamic Network Interactions Underpinning Cognition: A cTBS-fMRI Study of the Flexible Adaptive Neural System for Semantics. |
Q38387839 | Mapping the Multiple Graded Contributions of the Anterior Temporal Lobe Representational Hub to Abstract and Social Concepts: Evidence from Distortion-corrected fMRI. |
Q57171104 | Mapping the intersection of language and reading: the neural bases of the primary systems hypothesis |
Q59297673 | Mapping whole brain connectivity changes: The potential impact of different surgical resection approaches for temporal lobe epilepsy |
Q59297688 | Measuring language recovery in the underlying large‐scale neural network: Pulling together in the face of adversity |
Q38397540 | Mimicking aphasic semantic errors in normal speech production: evidence from a novel experimental paradigm |
Q59297684 | More evidence for a continuum between phonological and deep dyslexia: Novel data from three measures of direct orthography-to-phonology translation |
Q38423530 | Natural selection: the impact of semantic impairment on lexical and object decision |
Q34619679 | Neural basis of category-specific semantic deficits for living things: evidence from semantic dementia, HSVE and a neural network model |
Q30356638 | Neurocognitive insights on conceptual knowledge and its breakdown. |
Q38444645 | Non-verbal semantic impairment in semantic dementia. |
Q38444339 | Not lost in translation: generalization of the primary systems hypothesis to Japanese-specific language processes |
Q55385254 | Noun and verb processing in aphasia: Behavioural profiles and neural correlates. |
Q59297706 | Object recognition under semantic impairment: The effects of conceptual regularities on perceptual decisions |
Q59297708 | On the use of regression techniques for the analysis of single case aphasic data |
Q96222424 | Overarching Principles and Dimensions of the Functional Organization in the Inferior Parietal Cortex |
Q37989236 | Overview and ways forward for future research |
Q38495225 | Phonological learning in semantic dementia |
Q58256258 | Posterior middle temporal gyrus is involved in verbal and non-verbal semantic cognition: Evidence from rTMS |
Q59297689 | Postscript: SD-squared revisited again |
Q50149099 | Predicting the outcome of anomia therapy for people with aphasia post CVA: both language and cognitive status are key predictors |
Q90431938 | Predicting the pattern and severity of chronic post-stroke language deficits from functionally-partitioned structural lesions |
Q38486915 | Premorbid expertise produces category-specific impairment in a domain-general semantic disorder |
Q34470050 | Processing deficits for familiar and novel faces in patients with left posterior fusiform lesions |
Q58266345 | Progressive non-fluent aphasia is not a progressive form of non-fluent (post-stroke) aphasia |
Q40534540 | Reconnecting Cognitive Neuropsychology: Commentary on Harley's 'Does Cognitive Neuropsychology have a Future?' |
Q48087780 | Reconnecting with Joseph and Augusta Dejerine: 100 years on. |
Q59297690 | Recovery of Language and Reading in Post-CVA Aphasia: A Longitudinal Study |
Q95301448 | Redefining the multidimensional clinical phenotypes of frontotemporal lobar degeneration syndromes |
Q38402625 | Refractory effects in stroke aphasia: a consequence of poor semantic control |
Q58727632 | Relating resting-state hemodynamic changes to the variable language profiles in post-stroke aphasia |
Q38413958 | Relative preservation of 'animate' knowledge in an atypical presentation of herpes simplex virus encephalitis. |
Q58252883 | Relearning and retention of verbal labels in a case of semantic dementia |
Q38484079 | Relearning in semantic dementia reflects contributions from both medial temporal lobe episodic and degraded neocortical semantic systems: evidence in support of the complementary learning systems theory |
Q38496270 | Remembering 'zeal' but not 'thing': reverse frequency effects as a consequence of deregulated semantic processing |
Q59297681 | Repetition priming of picture naming in semantic aphasia: The impact of intervening items |
Q38479440 | Revealing and quantifying the impaired phonological analysis underpinning impaired comprehension in Wernicke's aphasia |
Q59297675 | Revealing the Dynamic Modulations That Underpin a Resilient Neural Network for Semantic Cognition: An fMRI Investigation in Patients With Anterior Temporal Lobe Resection |
Q91864994 | Revealing the neural networks that extract conceptual gestalts from continuously evolving or changing semantic contexts |
Q38495133 | Reverse concreteness effects are not a typical feature of semantic dementia: evidence for the hub-and-spoke model of conceptual representation |
Q37671813 | SD-squared revisited: reply to Coltheart, Tree, and Saunders (2010). |
Q38397334 | SD-squared: on the association between semantic dementia and surface dyslexia |
Q38377184 | Seeing the Meaning: Top-Down Effects on Letter Identification |
Q34137078 | Selective functional integration between anterior temporal and distinct fronto-mesolimbic regions during guilt and indignation |
Q38383725 | Selective short-term memory deficits arise from impaired domain-general semantic control mechanisms |
Q47635180 | Self-blame-Selective Hyperconnectivity Between Anterior Temporal and Subgenual Cortices and Prediction of Recurrent Depressive Episodes. |
Q38428529 | Semantic dementia with category specificity:acomparative case-series study |
Q38495605 | Semantic diversity accounts for the "missing" word frequency effect in stroke aphasia: insights using a novel method to quantify contextual variability in meaning |
Q38459728 | Semantic diversity: a measure of semantic ambiguity based on variability in the contextual usage of words |
Q38416636 | Semantic feature knowledge and picture naming in dementia of Alzheimer's type: a new approach |
Q34543849 | Semantic impairment in stroke aphasia versus semantic dementia: a case-series comparison |
Q59297709 | Semantic loss without surface dyslexia |
Q38421217 | Semantic memory is an amodal, dynamic system: Evidence from the interaction of naming and object use in semantic dementia |
Q35706464 | Semantic memory is impaired in patients with unilateral anterior temporal lobe resection for temporal lobe epilepsy |
Q30483686 | Semantic memory is key to binding phonology: converging evidence from immediate serial recall in semantic dementia and healthy participants |
Q38380360 | Semantic processing in the anterior temporal lobes: a meta-analysis of the functional neuroimaging literature. |
Q38461142 | Shapes, scents and sounds: quantifying the full multi-sensory basis of conceptual knowledge |
Q59125427 | Shared processes resolve competition within and between episodic and semantic memory: Evidence from patients with LIFG lesions |
Q36740993 | Sleep Spindle Density Predicts the Effect of Prior Knowledge on Memory Consolidation |
Q48290990 | Solving the paradox of the equipotential and modular brain: a neurocomputational model of stroke vs. slow-growing glioma |
Q38490466 | Staging of the cognitive decline in Alzheimer's disease: insights from a detailed neuropsychological investigation of mild cognitive impairment and mild Alzheimer's disease |
Q38423923 | Structure and deterioration of semantic memory: a neuropsychological and computational investigation |
Q99709838 | Subgenual activation and the finger of blame: individual differences and depression vulnerability |
Q38416411 | Surface dyslexia in semantic dementia: a comparison of the influence of consistency and regularity |
Q38498739 | Taking both sides: do unilateral anterior temporal lobe lesions disrupt semantic memory? |
Q39173421 | Targeted memory reactivation of newly learned words during sleep triggers REM-mediated integration of new memories and existing knowledge |
Q38393191 | Task-Related Dynamic Division of Labor Between Anterior Temporal and Lateral Occipital Cortices in Representing Object Size. |
Q47336917 | Task-based and resting-state fMRI reveal compensatory network changes following damage to left inferior frontal gyrus |
Q38428788 | Temporal lobe regions engaged during normal speech comprehension. |
Q92074618 | The Graded Change in Connectivity across the Ventromedial Prefrontal Cortex Reveals Distinct Subregions |
Q36754026 | The Nature and Neural Correlates of Semantic Association versus Conceptual Similarity |
Q36754036 | The Roles of Left Versus Right Anterior Temporal Lobes in Conceptual Knowledge: An ALE Meta-analysis of 97 Functional Neuroimaging Studies |
Q49916747 | The Roles of Left Versus Right Anterior Temporal Lobes in Semantic Memory: A Neuropsychological Comparison of Postsurgical Temporal Lobe Epilepsy Patients |
Q36534316 | The Semantic Network at Work and Rest: Differential Connectivity of Anterior Temporal Lobe Subregions. |
Q38393530 | The anterior temporal cortex is a primary semantic source of top-down influences on object recognition |
Q38375137 | The anterior temporal lobe semantic hub is a part of the language neural network: selective disruption of irregular past tense verbs by rTMS. |
Q37446754 | The anterior temporal lobes are critically involved in acquiring new conceptual knowledge: evidence for impaired feature integration in semantic dementia |
Q30442777 | The anterior temporal lobes support residual comprehension in Wernicke's aphasia |
Q47889227 | The anterior-ventrolateral temporal lobe contributes to boosting visual working memory capacity for items carrying semantic information |
Q37919899 | The application of errorless learning to aphasic disorders: A review of theory and practice |
Q34927638 | The association between semantic dementia and surface dyslexia in Japanese |
Q59509195 | The auditory agnosias |
Q52605906 | The behavioural patterns and neural correlates of concrete and abstract verb processing in aphasia: A novel verb semantic battery. |
Q47563140 | The contribution of executive control to semantic cognition: Convergent evidence from semantic aphasia and executive dysfunction |
Q38459389 | The degraded concept representation system in semantic dementia: damage to pan-modal hub, then visual spoke |
Q38478194 | The differential contributions of pFC and temporo-parietal cortex to multimodal semantic control: exploring refractory effects in semantic aphasia |
Q59297693 | The effects of decreasing and increasing cue therapy on improving naming speed and accuracy for verbs and nouns in aphasia |
Q107457307 | The immediate impact of transcranial magnetic stimulation on brain structure: short-term neuroplasticity following one session of cTBS |
Q58173273 | The impact of phonological or semantic impairment on delayed auditory repetition: Evidence from stroke aphasia and semantic dementia |
Q30494759 | The impact of semantic impairment on verbal short-term memory in stroke aphasia and semantic dementia: A comparative study |
Q38434821 | The influence of personal familiarity and context on object use in semantic dementia |
Q38408735 | The natural history of late-stage "pure" semantic dementia |
Q30395594 | The neural and computational bases of semantic cognition. |
Q91474436 | The neural and neurocomputational bases of recovery from post-stroke aphasia |
Q37199347 | The neural basis of conceptual-emotional integration and its role in major depressive disorder |
Q38390707 | The neural network for tool-related cognition: An activation likelihood estimation meta-analysis of 70 neuroimaging contrasts |
Q34798510 | The neural organization of semantic control: TMS evidence for a distributed network in left inferior frontal and posterior middle temporal gyrus |
Q49031532 | The relationship between phonological and morphological deficits in Broca's aphasia: further evidence from errors in verb inflection |
Q38480487 | The role of plasticity-related functional reorganization in the explanation of central dyslexias |
Q37196294 | The role of sleep spindles and slow-wave activity in integrating new information in semantic memory |
Q37314959 | The role of the anterior temporal lobes in the comprehension of concrete and abstract words: rTMS evidence |
Q38417130 | The role of the temporal lobe semantic system in number knowledge: evidence from late-stage semantic dementia |
Q50624167 | The roles of long-term phonotactic and lexical prosodic knowledge in phonological short-term memory. |
Q30450227 | The roles of the "ventral" semantic and "dorsal" pathways in conduite d'approche: a neuroanatomically-constrained computational modeling investigation |
Q47151711 | The structural connectivity of higher order association cortices reflects human functional brain networks |
Q38417051 | The timing of anterior temporal lobe involvement in semantic processing |
Q47140467 | The tract terminations in the temporal lobe: Their location and associated functions. |
Q51983837 | The treatment of anomia using errorless learning. |
Q58142390 | The use of cueing to alleviate recurrent verbal perseverations: Evidence from transcortical sensory aphasia |
Q59297682 | The variation of function across the human insula mirrors its patterns of structural connectivity: Evidence from in vivo probabilistic tractography |
Q38375428 | The ventral and inferolateral aspects of the anterior temporal lobe are crucial in semantic memory: evidence from a novel direct comparison of distortion-corrected fMRI, rTMS, and semantic dementia |
Q102211936 | The verbal, non-verbal and structural bases of functional communication abilities in aphasia |
Q59297677 | Time for a quick word? The striking benefits of training speed and accuracy of word retrieval in post-stroke aphasia |
Q35541568 | Time- but not sleep-dependent consolidation promotes the emergence of cross-modal conceptual representations |
Q58269013 | Towards theory‐driven therapies for aphasic verb impairments: A review of current theory and practice |
Q38409942 | Transport for language south of the Sylvian fissure: The routes and history of the main tracts and stations in the ventral language network |
Q59297702 | Treatment of anomia using errorless versus errorful learning: are frontal executive skills and feedback important? |
Q44952679 | Triangulation of language-cognitive impairments, naming errors and their neural bases post-stroke. |
Q35865685 | Triangulation of the neurocomputational architecture underpinning reading aloud |
Q54957844 | Unification of behavioural, computational and neural accounts of word production errors in post-stroke aphasia. |
Q59297700 | Unlocking the Nature of the Phonological–Deep Dyslexia Continuum: The Keys to Reading Aloud Are in Phonology and Semantics |
Q34499083 | Unlocking the nature of the phonological-deep dyslexia continuum: the keys to reading aloud are in phonology and semantics |
Q38478673 | Unpicking the semantic impairment in Alzheimer's disease: qualitative changes with disease severity. |
Q92317140 | Unveiling the dynamic interplay between the hub- and spoke-components of the brain's semantic system and its impact on human behaviour |
Q36092432 | Using a combination of fMRI and anterior temporal lobe rTMS to measure intrinsic and induced activation changes across the semantic cognition network |
Q58173328 | Using computational, parallel distributed processing networks to model rehabilitation in patients with acquired dyslexia: An initial investigation |
Q38410315 | Using errorless learning to treat letter-by-letter reading: contrasting word versus letter-based therapy |
Q30446428 | Using in vivo probabilistic tractography to reveal two segregated dorsal 'language-cognitive' pathways in the human brain |
Q46976531 | Using neurostimulation to understand the impact of pre-morbid individual differences on post-lesion outcomes |
Q36855266 | Using parallel distributed processing models to simulate phonological dyslexia: the key role of plasticity-related recovery |
Q37971815 | Using phonemic cueing of spontaneous naming to predict item responsiveness to therapy for anomia in aphasia |
Q37604807 | Using principal component analysis to capture individual differences within a unified neuropsychological model of chronic post-stroke aphasia: Revealing the unique neural correlates of speech fluency, phonology and semantics |
Q27303604 | Varieties of semantic 'access' deficit in Wernicke's aphasia and semantic aphasia |
Q59297695 | Varieties of silence: the impact of neuro-degenerative diseases on language systems in the brain |
Q38497668 | Ventrolateral prefrontal cortex plays an executive regulation role in comprehension of abstract words: convergent neuropsychological and repetitive TMS evidence. |
Q38479349 | Wernicke's aphasia reflects a combination of acoustic-phonological and semantic control deficits: a case-series comparison of Wernicke's aphasia, semantic dementia and semantic aphasia |
Q38432848 | What lies beneath: a comparison of reading aloud in pure alexia and semantic dementia |
Q38416626 | What underlies the neuropsychological pattern of irregular > regular past-tense verb production? |
Q38477362 | What's in a word? A parametric study of semantic influences on visual word recognition |
Q34111105 | When does less yield more? The impact of severity upon implicit recognition in pure alexia |
Q38420992 | When does word meaning affect immediate serial recall in semantic dementia? |
Q38428016 | When objects lose their meaning: what happens to their use? |
Q50894311 | Why bilateral damage is worse than unilateral damage to the brain. |
Q59297691 | “L” is for tiger: Effects of phonological (mis)cueing on picture naming in semantic aphasia |
Q59297683 | “W” is for bath: Can associative errors be cued? |