Zobrazeno 1 - 10
of 158
pro vyhledávání: '"Mark, Layton"'
Autor:
Wondimagegn Adissu, Marcelo Brito, Eduardo Garbin, Marcela Macedo, Wuelton Monteiro, Sandip Kumar Mukherjee, Jane Myburg, Mohammad Shafiul Alam, Germana Bancone, Pooja Bansil, Sampa Pal, Abhijit Sharma, Stephanie Zobrist, Andrew Bryan, Cindy S Chu, Santasabuj Das, Gonzalo J Domingo, Amanda Hann, James Kublin, Marcus V G Lacerda, Mark Layton, Benedikt Ley, Sean C Murphy, Francois Nosten, Dhélio Pereira, Ric N Price, Arunansu Talukdar, Daniel Yilma, Emily Gerth-Guyette
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 17, Iss 10, p e0011652 (2023)
IntroductionScreening for G6PD deficiency can inform disease management including malaria. Treatment with the antimalarial drugs primaquine and tafenoquine can be guided by point-of-care testing for G6PD deficiency.Methods and findingsData from simil
Externí odkaz:
https://doaj.org/article/6046749186634df9825ceec3ba9bb654
Autor:
Hanny Al-Samkari, Rachael F. Grace, Andreas Glenthøj, Oliver Andres, Wilma Barcellini, Frédéric Galacteros, Kevin H. M. Kuo, D. Mark Layton, Marta Morado, Vip Viprakasit, Feng Tai, Rolandas Urbstonaitis, Jaime Morales, Bryan McGee, Eduard J. van Beers
Publikováno v:
Haematologica, Vol 109, Iss 3 (2023)
Externí odkaz:
https://doaj.org/article/ab780d6e13964b4ab15a635f78853845
Autor:
Dagmar Pospíŝilová, Rachael F. Grace, Andreas Glenthøj, Carl Lander, Eduard van Beers, Bertil Glader, Mark Layton, Kevin H.M. Kuo, Juan-Luis Vives-Corrons, Yan Yan, Bryan Mcgee, Sara Higa, Paola Bianchi
Publikováno v:
HemaSphere, Vol 7, p e7441867 (2023)
Externí odkaz:
https://doaj.org/article/3346183076b44ce3a981b4e320bbabe0
Autor:
Hanny Al-Samkari, Rachael F. Grace, Andreas Glenthøj, Wilma Barcellini, Madeleine Verhovsek, Jennifer A. Rothman, Marta Morado, Mark Layton, Oliver Andres, Frédéric Galactéros, Koichi Onodera, Satheesh Chonat, Rengyi Xu, Bryan Mcgee, Melissa Dibacco, Jaime Morales, Eduard van Beers
Publikováno v:
HemaSphere, Vol 7, p e918756f (2023)
Externí odkaz:
https://doaj.org/article/98a90c4c08194ed792fae1ec439a28c7
Autor:
Yan Yan, Junlong Li, D Mark Layton, Rachael F Grace, Vip Viprakasit, Eduard J van Beers, Joan-Lluis Vives Corrons, Bertil Glader, Andreas Glenthøj, Hitoshi Kanno, Kevin H M Kuo, Carl Lander, Dagmar Pospíŝilová, Audra N Boscoe, Chris Bowden, Paola Bianchi
Publikováno v:
BMJ Open, Vol 13, Iss 3 (2023)
Introduction Pyruvate kinase (PK) deficiency is a rare, under-recognised, hereditary condition that leads to chronic haemolytic anaemia and potentially serious secondary complications, such as iron overload, cholecystitis, pulmonary hypertension and
Externí odkaz:
https://doaj.org/article/0e05ba4c19b7445195a337fe6be613f1
Autor:
Noémi B. A. Roy, Lydie Da Costa, Roberta Russo, Paola Bianchi, Maria del Mar Mañú-Pereira, Elisa Fermo, Immacolata Andolfo, Barnaby Clark, Melanie Proven, Mayka Sanchez, Richard van Wijk, Bert van der Zwaag, Mark Layton, David Rees, Achille Iolascon, on behalf of the British Society for Haematology and the European Hematology Association
Publikováno v:
HemaSphere, Vol 6, Iss 6, p e739 (2022)
Externí odkaz:
https://doaj.org/article/9374bbd49e7c4657be3e9a7c2dd0e7d2
Autor:
Hanne Stotesbury, Jamie M. Kawadler, Jonathan D. Clayden, Dawn E. Saunders, Anna M. Hood, Melanie Koelbel, Sati Sahota, David C. Rees, Olu Wilkey, Mark Layton, Maria Pelidis, Baba P. D. Inusa, Jo Howard, Subarna Chakravorty, Chris A. Clark, Fenella J. Kirkham
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Research in sickle cell anemia (SCA) has used, with limited race-matched control data, binary categorization of patients according to the presence or absence of silent cerebral infarction (SCI). SCI have primarily been identified using low-resolution
Externí odkaz:
https://doaj.org/article/b9b954bad2e74950bfb278ad5b115405
Autor:
Hanne Stotesbury, Patrick W. Hales, Anna M. Hood, Melanie Koelbel, Jamie M. Kawadler, Dawn E. Saunders, Sati Sahota, David C. Rees, Olu Wilkey, Mark Layton, Maria Pelidis, Baba P. D. Inusa, Jo Howard, Subarna Chakravorty, Chris A. Clark, Fenella J. Kirkham
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Previous studies have pointed to a role for regional cerebral hemodynamic stress in neurological complications in patients with sickle cell anemia (SCA), with watershed regions identified as particularly at risk of ischemic tissue injury. Using singl
Externí odkaz:
https://doaj.org/article/72f7c88f701c47aea7fb2b9583d683dc
Autor:
Ana Rio-Machin, Tom Vulliamy, Nele Hug, Amanda Walne, Kiran Tawana, Shirleny Cardoso, Alicia Ellison, Nikolas Pontikos, Jun Wang, Hemanth Tummala, Ahad Fahad H. Al Seraihi, Jenna Alnajar, Findlay Bewicke-Copley, Hannah Armes, Michael Barnett, Adrian Bloor, Csaba Bödör, David Bowen, Pierre Fenaux, Andrew Green, Andrew Hallahan, Henrik Hjorth-Hansen, Upal Hossain, Sally Killick, Sarah Lawson, Mark Layton, Alison M. Male, Judith Marsh, Priyanka Mehta, Rogier Mous, Josep F. Nomdedéu, Carolyn Owen, Jiri Pavlu, Elspeth M. Payne, Rachel E. Protheroe, Claude Preudhomme, Nuria Pujol-Moix, Aline Renneville, Nigel Russell, Anand Saggar, Gabriela Sciuccati, David Taussig, Cynthia L. Toze, Anne Uyttebroeck, Peter Vandenberghe, Brigitte Schlegelberger, Tim Ripperger, Doris Steinemann, John Wu, Joanne Mason, Paula Page, Susanna Akiki, Kim Reay, Jamie D. Cavenagh, Vincent Plagnol, Javier F. Caceres, Jude Fitzgibbon, Inderjeet Dokal
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
Familial myeloid malignancies have recently been classified as separate disease entities. Here, using whole-exome sequencing of affected pedigrees - the authors highlight genetic variants associated with these conditions.
Externí odkaz:
https://doaj.org/article/a25bb12eaf454851a551304c03cbab09
Autor:
Sampa Pal, Jane Myburgh, Pooja Bansil, Amanda Hann, Lynn Robertson, Emily Gerth-Guyette, Gwen Ambler, Greg Bizilj, Maria Kahn, Stephanie Zobrist, Michelle R Manis, Nickolas A Styke, Vajra Allan, Richard Ansbro, Tobi Akingbade, Andrew Bryan, Sean C Murphy, James G Kublin, Mark Layton, Gonzalo J Domingo
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0257560 (2021)
Certain clinical indications and treatments such as the use of rasburicase in cancer therapy and 8-aminoquinolines for Plasmodium vivax malaria treatment would benefit from a point-of-care test for glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Externí odkaz:
https://doaj.org/article/af90750e5f424c59a8c771e3f4e6f118