Zobrazeno 1 - 10 of 75 pro vyhledávání: '"Richard O Robinson"'
2
Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies?
Autor: Robert G. Will, Anne Marie Winstone, Evangeline Wassmer, Sameer M. Zuberi, Michael Pike, Alison Powell, Carlos de Sousa, Peter Baxter, Manju A. Kurian, Suvankar Pal, Robert McFarland, Richard O. Robinson, Paul Gissen, Christopher M Verity, John H. Livingston
Publikováno v: Verity, C, Winstone, A M, Will, R, Powell, A, Baxter, P, De Sousa, C, Gissen, P, Kurian, M, Livingston, J, Mcfarland, R, Pal, S, Pike, M, Robinson, R, Wassmer, E & Zuberi, S 2018, ' Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies? ', Archives of Disease in Childhood, pp. archdischild-2018-315458 . https://doi.org/10.1136/archdischild-2018-315458
Archives of Disease in Childhood
ObjectivesTo report investigations performed in children with progressive neurodegenerative diseases reported to this UK study.DesignSince 1997 paediatric surveillance for variant Creutzfeldt-Jakob disease (vCJD) has been performed by identifying chi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f3f5435299d4454f59be5b7d3491ae3
https://hdl.handle.net/20.500.11820/c72334e0-ce9c-4c0e-8ef0-58b74bf6f05c
Zobrazit plný text záznamu
3
Non-invasive detection and quantification of human foetal brain lactatein uteroby magnetic resonance spectroscopy
Autor: W. Jan, Stephen F. Keevil, Richard O. Robinson, Darryl Maxwell, Meekai To, Geoffrey Charles-Edwards
Publikováno v: Prenatal Diagnosis. 30:260-266
Objective To assess the feasibility of foetal cerebral lactate detection and quantification by proton magnetic resonance spectroscopy (1H-MRS) in pregnancies at increased risk of cerebral hypoxia, using a clinical 1.5 T magnetic resonance imaging (MR
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4f7ea772c97a742f08194e25cc4e12df
https://doi.org/10.1002/pd.2463
Zobrazit plný text záznamu
4
Psychotic and severe behavioural reactions with vigabatrin: a review
Autor: Richard O. Robinson, C. D. Ferrie, Chrysostomos P. Panayiotopoulos
Publikováno v: Acta Neurologica Scandinavica. 93:1-8
Behavioural disturbances and psychotic reactions are commoner in patients with epilepsy than in the general population and may be precipitated by the majority of antiepileptic drugs, including the newer ones. These reactions may be more frequent in p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f63baedc4ae88e46a1b3c648302ac1b3
https://doi.org/10.1111/j.1600-0404.1996.tb00161.x
Zobrazit plný text záznamu
6
Childhood Moyamoya Presenting as Dementia: Report of a Case
Autor: Richard O. Robinson, S. D. Levin, R. D. Hoare
Publikováno v: Developmental Medicine & Child Neurology. 25:794-797
SUMMARY A case is presented of moyamoya disease in an Anglo-Saxon child whose principal clinical feature, uniquely, was dementia. CT findings were unexplainable so angiography was performed. Moyamoya is an angiographic entity which has been associate
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aba123412179cffa8ef50729c99d3d9
https://doi.org/10.1111/j.1469-8749.1983.tb13848.x
Zobrazit plný text záznamu
7
Voluntary hand movements and brain relations
Autor: Richard O. Robinson
Publikováno v: Developmental Medicine & Child Neurology. 40:780-784
Very little is known directly about the physiology of central movement control in the child. Anatomy is inferred from primate studies, largely those of the macaque monkey. Brain-behaviour relations are derived from adult volunteers, most recently usi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abae787db0030d9767081a84febbf61f
https://doi.org/10.1111/j.1469-8749.1998.tb12348.x
Zobrazit plný text záznamu
9
Molybdenum cofactor deficiency - phenotypic variability in a family with a late-onset variant
Autor: H A Simmonds, Lynette D. Fairbanks, Richard O. Robinson, E F Hughes
Publikováno v: Developmental Medicine & Child Neurology. 40:57-61
In a family with molybdenum cofactor deficiency, the onset in the index case was delayed until 1 year of age, when the patient presented with an episode of lethargy and inconsolable crying culminating in a seizure. By 17 months she showed mild motor
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfdd778c9220f766af24c40102ba279f
https://doi.org/10.1111/j.1469-8749.1998.tb15357.x
Zobrazit plný text záznamu
10
Salla disease - rare or underdiagnosed?
Autor: Richard O. Robinson, Brian D. Lake, Anthony H. Fensom
Publikováno v: Developmental Medicine & Child Neurology. 39:153-157
Salla disease is described in two English children. Eighty-seven of the 89 cases so far reported come from Finland. It may be genuinely rare outside Finland or possibly underdiagnosed. Although a lysosomal disorder, it lacks many of their more charac
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2110924b9d12284648cf0ed021fa6452
https://doi.org/10.1111/j.1469-8749.1997.tb07403.x
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje