Zobrazeno 1 - 10
of 22
pro vyhledávání: '"C H, Salmond"'
Autor:
Patrick Smith, Peter K Thompson, C. H. Salmond, Edward Glucksman, Richard Meiser-Stedman, Tim Dalgleish
Publikováno v:
Journal of Child Psychology and Psychiatry. 52:560-570
Background: There is increasing theoretical, clinical and research evidence for the role of trauma memory in the aetiology of acute pathological stress responses in adults. However, research into the phenomenology of trauma memories in young people i
Autor:
Faraneh Vargha-Khadem, C. H. Salmond, David G. Gadian, Karl J. Friston, John Ashburner, Alan Connelly
Publikováno v:
European Journal of Neuroscience. 22:764-772
The neural basis of autistic spectrum disorders (ASDs) is poorly understood. Studies of mnemonic function in ASD suggest a profile of impaired episodic memory with relative preservation of semantic memory (at least in high-functioning individuals). S
Autor:
Faraneh Vargha-Khadem, Karl J. Friston, C. H. Salmond, John Ashburner, David G. Gadian, Alan Connelly
Publikováno v:
NeuroImage. 17:1027-1030
In this paper we address the assumptions about the distribution of errors made by voxel-based morphometry. Voxel-based morphometry (VBM) uses the general linear model to construct parametric statistical tests. In order for these statistics to be vali
Publikováno v:
Journal of child psychology and psychiatry, and allied disciplines. 52(5)
There is increasing theoretical, clinical and research evidence for the role of trauma memory in the aetiology of acute pathological stress responses in adults. However, research into the phenomenology of trauma memories in young people is currently
© Cambridge University Press 2008 and Cambridge University Press, 2009. Introduction Autistic spectrum disorders (ASDs) are characterized by impairments in social interaction and communication, and by restricted or repetitive behaviours and interest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54fbe279022cf4d99b8e2f9ed37f758a
https://doi.org/10.1017/cbo9780511490101.006
https://doi.org/10.1017/cbo9780511490101.006
Publikováno v:
Cortex; a journal devoted to the study of the nervous system and behavior. 43(6)
Autistic spectrum disorder (ASD) refers to a heterogeneous group of social communication problems. Research into the neural basis of ASD has revealed abnormalities in a number of different regions of the brain. However, the literature is highly incon
Autor:
J D, Pickard, P J, Hutchinson, J P, Coles, L A, Steiner, A J, Johnston, T D, Fryer, M R, Coleman, P, Smielewski, D A, Chatfield, F, Aigbirhio, G B, Williams, K, Rice, J C, Clark, C H, Salmond, B J, Sahakian, P G, Bradley, T A, Carpenter, R, Salvador, A, Pena, J H, Gillard, A S, Cunningham, S, Piechnik, M, Czosnyka, D K, Menon
Publikováno v:
Acta neurochirurgica. Supplement. 95
The heterogeneity of the initial insult and subsequent pathophysiology has made both the study of human head injury and design of randomised controlled trials exceptionally difficult. The combination of multimodality bedside monitoring and functional
Autor:
C. H. Salmond, Faraneh Vargha-Khadem, David G. Gadian, K. J. Friston, Kate E. Watkins, Mortimer Mishkin
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 100(17)
Hypoxic–ischemic events sustained within the first year of life can result in developmental amnesia, a disorder characterized by markedly impaired episodic memory and relatively preserved semantic memory, in association with medial temporal patholo
Publikováno v:
Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 358(1430)
Autism is a psychiatric syndrome characterized by impairments in three domains: social interaction, communication, and restricted and repetitive behaviours and interests. Recent findings implicate the amygdala in the neurobiology of autism. In this p
Publikováno v:
Hum Brain Mapp
The KE family is a large three‐generational pedigree in which half of the members suffer from a verbal and orofacial dyspraxia in association with a point mutation in the FOXP2 gene. This report extends previous voxel‐based morphometric analyses