Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jeremy M W, Kirk"'
Autor:
Sonika Sethi, Aditi Kumar, Anandadeep Mandal, Mohammed Shaikh, Claire A. Hall, Jeremy M. W. Kirk, Paul Moss, Matthew J. Brookes, Supratik Basu
Publikováno v:
Trials, Vol 22, Iss 1, Pp 1-12 (2021)
Abstract Background Developing a safe and effective vaccine will be the principal way of controlling the COVID-19 pandemic. However, current COVID-19 vaccination trials are not adequately representing a diverse participant population in terms of age,
Externí odkaz:
https://doaj.org/article/53ddeeeb7e934e9493021617a2874d8b
Autor:
Matthew J Brookes, Aditi Kumar, Supratik Basu, Sonika Sethi, Anandadeep Mandal, Mohammed Shaikh, Claire A Hall, Jeremy M W Kirk, Paul Moss
Publikováno v:
BMJ Open, Vol 11, Iss 6 (2021)
Objective A key challenge towards a successful COVID-19 vaccine uptake is vaccine hesitancy. We examine and provide novel insights on the key drivers and barriers towards COVID-19 vaccine uptake.Design This study involved an anonymous cross-sectional
Externí odkaz:
https://doaj.org/article/3190d61a98134298a3ed57f2dbd63981
Autor:
Emmie N Upners, Lars Lau Raket, Jørgen H Petersen, Ajay Thankamony, Edna Roche, Guftar Shaikh, Jeremy M W Kirk, Hilary Hoey, Sten-A Ivarsson, Olle Söder, Anders Juul, Rikke Beck Jensen
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
Autor:
Anandadeep Mandal, Sonika Sethi, Aditi Kumar, Paul Moss, Mohammed Shaikh, Supratik Basu, Matthew J Brookes, Jeremy M. W. Kirk, Claire A. Hall
Publikováno v:
Trials
Trials, Vol 22, Iss 1, Pp 1-12 (2021)
Trials, Vol 22, Iss 1, Pp 1-12 (2021)
Background Developing a safe and effective vaccine will be the principal way of controlling the COVID-19 pandemic. However, current COVID-19 vaccination trials are not adequately representing a diverse participant population in terms of age, ethnicit
Autor:
Martin O, Savage, Raja, Padidela, Jeremy M W, Kirk, Alexsandra C, Malaquias, Alexander A L, Jorge
Publikováno v:
Pediatric endocrinology reviews : PER. 6
Noonan syndrome (NS) is a phenotypically heterogeneous condition frequently associated with short stature. Genetic investigations have identified mutations in several genes, e.g. PTPN11, KRAS, RAF and SOS1 in patients with the NS phenotype and relate
Autor:
Basia K, Bielinski, Phil J, Darbyshire, Lynne, Mathers, Nicola J, Crabtree, Jeremy M W, Kirk, Heather F, Stirling, Nick J, Shaw
Publikováno v:
British journal of haematology. 120(2)
Reduction of bone density and its associated morbidity is recognized in young adults with beta-thalassaemia major, but the aetiology is not clear. This study used dual X-ray absorptiometry (DXA) to look at bone mineral apparent density (BMAD) in chil
Publikováno v:
Medical and pediatric oncology. 20(3)
Serum thyroglobulin has been measured serially in ten children aged 5-17 years presenting with differentiated thyroid carcinoma. At presentation 4 had intra-thyroidal disease, 3 had lymph node metastases, and 3 had lung metastases. During follow-up f