E
Elizabeth Chalmers
Researcher at Royal Hospital for Sick Children
Publications - 82
Citations - 5763
Elizabeth Chalmers is an academic researcher from Royal Hospital for Sick Children. The author has contributed to research in topics: Haemophilia & Haemophilia A. The author has an hindex of 31, co-authored 78 publications receiving 4938 citations. Previous affiliations of Elizabeth Chalmers include Western Infirmary & Glasgow Royal Infirmary.
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Journal ArticleDOI
Antithrombotic Therapy in Neonates and Children: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition)
Paul Monagle,Elizabeth Chalmers,Anthony K.C. Chan,Gabrielle deVeber,Fenella J. Kirkham,Patricia Massicotte,Alan D. Michelson +6 more
TL;DR: Within this chapter, the majority of recommendations are separate for neonates and children, reflecting the significant differences in epidemiology of thrombosis and safety and efficacy of therapy in these two populations.
Journal ArticleDOI
The rare coagulation disorders – review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation
Paula H. B. Bolton-Maggs,D. J. Perry,Elizabeth Chalmers,L. A. Parapia,Jonathan T. Wilde,Michael Williams,Peter William Collins,Steve Kitchen,Gerry Dolan,Andrew D Mumford +9 more
TL;DR: This review summarizes the current literature for disorders of fibrinogen, and deficiencies of prothrombin, factor V, FV’+ VIII, FVII, FX, the combined vitamin K‐dependent factors, FXI and FXIII with a section on Ehlers‐Danlos Syndrome.
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Antithrombotic therapy in children: the Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy.
TL;DR: This article about antithrombotic therapy in children is part of the 7th American College of Chest Physicians Conference on AntithromBotic and Thrombolytic Therapy: Evidence-Based Guidelines.
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A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO
Paula H. B. Bolton-Maggs,Elizabeth Chalmers,Peter William Collins,Paul Harrison,Stephen Kitchen,Ri Liesner,Adrian Minford,Andrew D Mumford,L. A. Parapia,David J. Perry,Steve P. Watson,Jonathan T. Wilde,Michael Williams +12 more
TL;DR: This review discusses the inherited platelet disorders summarising the current state of the art with respect to investigation and diagnosis and suggests how to manage bleeding manifestations with particular attention to surgical interventions and the management of pregnancy.
Journal ArticleDOI
Intensity of factor VIII treatment and inhibitor development in children with severe hemophilia A: the RODIN study
Samantha C. Gouw,H. Marijke van den Berg,Krista Fischer,Guenter Auerswald,Manuel Carcao,Elizabeth Chalmers,Hervé Chambost,Karin Kurnik,Ri Liesner,Pia Petrini,Helen Platokouki,Carmen Altisent,Johannes Oldenburg,Beatrice Nolan,Rosario Perez Garrido,M Elisa Mancuso,Anne Rafowicz,Michael Williams,Niels Clausen,Rutger A. Middelburg,Rolf Ljung,Johanna G. van der Bom +21 more
TL;DR: It is suggested that in previously untreated patients with severe hemophilia A, high-dosed intensive FVIII treatment increases inhibitor risk and prophylactic FV III treatment decreases inhibitor risk, especially in patients with low-risk F8 mutations.