Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kirsty L O'Donovan"'
Autor:
Nick Pollard, Laura McQuillin, Samantha Armitage, Jenny Featherstone, Kirsty L. O’Donovan, Sarah Longley
Publikováno v:
Review Journal of Autism and Developmental Disorders. 6:85-95
© 2018, Springer Science+Business Media, LLC, part of Springer Nature. Parents of children with autism spectrum disorders should have access to interventions to help them understand and support their child. This literature review examines the existi
Autor:
Gillian P. Bates, Hugh Rickards, Oliver Quarrell, Nicholas Stoy, Maria Björkqvist, Nils Wierup, David S Sanders, Eva Ekblad, Andrew C McCourt, Anne Elizabeth Rosser, Kirsty L O'Donovan, Elin Sand, David Craufurd
Publikováno v:
PLoS Currents
PLoS Currents; 7 (2015)
PLoS Currents; 7 (2015)
Weight loss is an important complication of Huntington's disease (HD), however the mechanism for weight loss in HD is not entirely understood. Mutant huntingtin is expressed in the gastrointestinal (GI) tract and, in HD mice, mutant huntingtin inclus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f02f56783429b07e25efd3a85f662d55
http://lup.lub.lu.se/record/8235202
http://lup.lub.lu.se/record/8235202
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 83:A44.3-A45
In the later stages of HD, Percutaneous Endoscopic Gastrostomy (PEG) feeding is considered an alternative or supplement to oral feeding. As part of a wider study, qualitative analysis was used on data from semi structured interviews on the decision m
Autor:
Helen Santini, Ferdinando Squitieri, Roger A. Barker, Lisa Robertson, Maria Rakowicz, G. Bernhard Landwehrmeyer, Oliver Quarrell, Kirsty L O'Donovan
Publikováno v:
PLoS Currents
Background The clinical presentation of Juvenile Huntington's Disease (JHD) can be very different from adult-onset HD with little evidence to guide symptomatic management. Aim To survey the current use of pharmacological treatments for JHD. Methods P
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 81:A21.3-A21
Cases of juvenile Huntington9s disease (JHD) represent the severe end of the phenotypic spectrum of HD. The first detailed description of JHD was written in German by Hoffmann in 1888. We have translated the article and report the description of two
Autor:
G B Landwehrmeyer, M Ramos-Arroyo, Kirsty L O'Donovan, N Peppa, C Dumoulin, I Biunno, O Handley, P Bauer, Oliver Quarrell
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 81:A20.1-A20
Aim The European Huntington9s Disease Network REGISTRY project analyses CAG repeat length measurements centrally which can be compared with the original laboratory result held at the local study site from 15 countries. We aimed to assess the extent o
Publikováno v:
Scopus-Elsevier
PLoS Currents
PLoS Currents
Juvenile Huntington's disease (JHD) is usually defined as Huntington's disease with an onset ≤ 20 years. The proportion of JHD cases reported in studies of Huntington's disease (HD) varies. A review of the literature found 62 studies that reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aad41ed9eb6313f611cd995c79af098c
http://www.scopus.com/inward/record.url?eid=2-s2.0-84873445971&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84873445971&partnerID=MN8TOARS