Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Sara Trompeter"'
Autor:
Anna M. Hood, Hanne Stotesbury, Melanie Kölbel, Michelle DeHaan, Michelle Downes, Jamie M. Kawadler, Satwinder Sahota, Dagmara Dimitriou, Baba Inusa, Olu Wilkey, Maria Pelidis, Sara Trompeter, Andrea Leigh, Janine Younis, Emma Drasar, Subarna Chakravorty, David C. Rees, Sue Height, Sarah Lawson, Johanna Gavlak, Atul Gupta, Deborah Ridout, Christopher A. Clark, Fenella J. Kirkham
Publikováno v:
Trials, Vol 22, Iss 1, Pp 1-18 (2021)
Abstract Background Young children with sickle cell anaemia (SCA) often have slowed processing speed associated with reduced brain white matter integrity, low oxygen saturation, and sleep-disordered breathing (SDB), related in part to enlarged adenoi
Externí odkaz:
https://doaj.org/article/95ccb568d8914dc086a76621449510c3
Autor:
Dimitrios Farmakis, John Porter, Ali Taher, Maria Domenica Cappellini, Michael Angastiniotis, Androulla Eleftheriou, for the 2021 TIF Guidelines Taskforce, Ali Alassaf, Emanuele Angelucci, Yesim Aydinok, Rayan Bou-Fakhredin Rayan, Loris Brunetta, George Constantinou, Shahina Daar, Vincenzo De Sanctis, Geoffrey Dusheiko, Riyad Elbard, Perla Eleftheriou, Panos Englezos, Dru Haines, Faiez N Hattab, George Kaltsounis, Antonios Kattamis, John Koskinas, Navdeep Kumar, Andreas Kulozik, Andreas Kyriakou, Aurelio Maggio, Roanna Maharai, Lauren Mednick, Eleni Michalaki, Wendy Murphy, Lena Oevermann, Raffaella Origa, Penelope-Georgia Papayanni, Constantina Politis, Farukh Shah, Anton Skafi, Nikos Skordis, Pietro Sodani, Ashraf Soliman, Seni Subair, Maria Tampaki, Sara Trompeter, Shobha Tuli, Malcolm Walker, Robert Yamashita, Evangelia Yannaki, Anne Yardumian
Publikováno v:
HemaSphere, Vol 6, Iss 8, p e732 (2022)
Beta-thalassemia and particularly its transfusion-dependent form (TDT) is a demanding clinical condition, requiring life-long care and follow-up, ideally in specialized centers and by multidisciplinary teams of experts. Despite the significant progre
Externí odkaz:
https://doaj.org/article/e09c27ab622646e18fe28c7d0ec0779e
Autor:
Rachel A. Smith, Tosti J. Mankelow, Despoina Drizou, Thomas Bullock, Tom Latham, Sara Trompeter, Allison Blair, David J. Anstee
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Sickle cell disease (SCD) is one of the most common inherited single gene disorders. Polymerisation of sickle hemoglobin results in erythrocytes that are inflexible and adherent, leading to coagulation, vascular and cellular activation and r
Externí odkaz:
https://doaj.org/article/80b26d17fb7b4680be25d1d650c7b9a6
Autor:
Paul Telfer, Josu de la Fuente, Mamta Sohal, Ralph Brown, Perla Eleftheriou, Noémi Roy, Frédéric B. Piel, Subarna Chakravorty, Kate Gardner, Mark Velangi, Emma Drasar, Farrukh Shah, John B. Porter, Sara Trompeter, Wale Atoyebi, Richard Szydlo, Kofi A. Anie, Kate Ryan, Joseph Sharif, Josh Wright, Emma Astwood, C. Sarah Nicolle, Amy Webster, David J. Roberts, Sanne Lugthart, Banu Kaya, Moji Awogbade, David C. Rees, Rob Hollingsworth, Baba Inusa, Jo Howard, D. Mark Layton
Publikováno v:
Haematologica, Vol 105, Iss 11 (2020)
Externí odkaz:
https://doaj.org/article/6c8eb0ee441b42e3b6284c91f79e18c8
Autor:
Terry Segal, Emma Harewood, Sara Stoneham, Sara Trompeter, Natalia Zarate-Lopez, Corinne Fisher, Elaine Murphy, Sara McCartney, Helen Simpson
Publikováno v:
Poster.
Autor:
David J. Anstee, Tom Latham, Sara Trompeter, Thomas Bullock, Allison Blair, Tosti J. Mankelow, Despoina Drizou, Rachel A. Smith
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Mankelow, T J, Drizou, D, Bullock, T E, Latham, T, Blair, A & Anstee, D J 2021, ' Large red cell-derived membrane particles are major contributors to hypercoagulability in sickle cell disease ', Scientific Reports, vol. 11, no. 1, 11035 . https://doi.org/10.1038/s41598-021-90477-z
Scientific Reports
Mankelow, T J, Drizou, D, Bullock, T E, Latham, T, Blair, A & Anstee, D J 2021, ' Large red cell-derived membrane particles are major contributors to hypercoagulability in sickle cell disease ', Scientific Reports, vol. 11, no. 1, 11035 . https://doi.org/10.1038/s41598-021-90477-z
Scientific Reports
Sickle cell disease (SCD) is one of the most common inherited single gene disorders. Polymerisation of sickle hemoglobin results in erythrocytes that are inflexible and adherent, leading to coagulation, vascular and cellular activation and resultant
Publikováno v:
Open Access Government. 37:42-43
Genetics and machine learning can improve blood transfusion outcomes The availability of blood for blood transfusion support is critical for the delivery of medical care. When a person donates blood, it is separated into different components: red cel
Autor:
Jeremie H. Estepp, Ram Kalpatthi, Gerald Woods, Sara Trompeter, Robert I. Liem, Kacie Sims, Adlette Inati, Baba P. D. Inusa, Andrew Campbell, Connie Piccone, Miguel R. Abboud, Kim Smith‐Whitley, Sandra Dixon, Margaret Tonda, Carla Washington, Noelle M. Griffin, Clark Brown
Publikováno v:
Pediatric bloodcancerREFERENCES. 69(8)
Sickle cell disease (SCD) is a devastating, multisystemic disorder that affects millions of people worldwide. The earliest clinical manifestations of SCD can affect infants as young as 6 months of age, and pediatric patients are at risk for acute and
Autor:
Alison J Deary, Ana Mora, D Poles, Esther Wong, Paula H B Bolton-Maggs, Lise J Estcourt, Alison Watt, Sara Trompeter, David Collett
Publikováno v:
Transfusion Medicine. 30:456-466
Objectives To establish, in an unselected population of London haemoglobinopathy patients, transfusion requirements, blood antigens/alloantibodies, transfusion modalities, burden of transfusion reactions and donor exposure. Background Haemoglobinopat
Autor:
Emma Astwood, Josh Wright, Joseph Sharif, Mark Velangi, Amy P. Webster, Paul Telfer, Wale Atoyebi, Noémi B. A. Roy, D. Mark Layton, Banu Kaya, Jo Howard, Sara Trompeter, Mamta Sohal, Moji Awogbade, C. Sarah Nicolle, Kate Ryan, Rob Hollingsworth, Josu de la Fuente, Richard Szydlo, Emma Drasar, Kate Gardner, Baba Inusa, David C. Rees, Farrukh Shah, Subarna Chakravorty, John Porter, Perla Eleftheriou, Sanne Lugthart, Ralph Brown, Kofi A. Anie, Frédéric B. Piel, David J. Roberts
Publikováno v:
Haematologica