Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Carey-Anne Eddy"'
Autor:
Dan M. Roden, Jackie Crawford, Seo-Kyung Chung, Wei Zhang, Ping Yang, Andrew N. Shelling, Caroline H. McCulley, Judith M. MacCormick, Carey–Anne Eddy, Mark I. Rees, Jonathan G. L. Mullins, John K. French, Tao Yang, Jonathan R. Skinner
Background— Inherited long-QT syndrome is characterized by prolonged QT interval on the ECG, syncope, and sudden death caused by ventricular arrhythmia. Causative mutations occur mostly in cardiac potassium and sodium channel subunit genes. Confide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa3d55dd33d05c2a5bbebebeafec036b
https://cronfa.swan.ac.uk/Record/cronfa10138
https://cronfa.swan.ac.uk/Record/cronfa10138
Autor:
Jonathan R. Skinner, John K. French, Hugh McAlister, Jackie Crawford, Judith M. MacCormick, Mark I. Rees, Andrew N. Shelling, Ian Crozier, Carey-Anne Eddy
Publikováno v:
Annals of emergency medicine. 54(1)
Study objective Long QT syndrome has significant mortality, which is reduced with appropriate management. It is known that long QT syndrome masquerades as other conditions, including seizure disorders. We aim to evaluate a series of patients with gen
Autor:
Judith M. MacCormick, Donald R. Love, Jonathan R. Skinner, Mark I. Rees, Seo-Kyung Chung, Carey-Anne Eddy, Jackie Crawford, Andrew N. Shelling
Background Sequencing or denaturing high-performance liquid chromatography (dHPLC) analysis of the known genes associated with the long QT syndrome (LQTS) fails to identify mutations in approximately 25% of subjects with inherited LQTS. Large gene de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88d3c189eb8b68cc787890740adbde19
https://cronfa.swan.ac.uk/Record/cronfa13972
https://cronfa.swan.ac.uk/Record/cronfa13972
Autor:
Patrick Gladding, Donald R. Love, Andrew N. Shelling, A. Vaughan, Jackie Crawford, Carey-Anne Eddy, Jonathan R. Skinner, M. Rees
Publikováno v:
Heart, Lung and Circulation. 18:S82
Functional variants of antioxidant genes in smokers with COPD and in those with normal lung function
Autor:
J. Garrett, T E Eaton, Graham Mills, Mark I. Rees, Robert P. Young, Greg D. Gamble, Carey-Anne Eddy, Peter N. Black, Lian Wu, Raewyn J. Hopkins
Publikováno v:
Respiratory Medicine: COPD Update. 1:141
Background: Chronic obstructive pulmonary disease (COPD) is predominantly the consequence of chronic smoking exposure, but its development may be influenced by genetic variants that affect lung remodelling, inflammation, and defence from oxidant stre