Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Maadh Aldouri"'
Autor:
Abdulsalam Al-Ani, Hazim Ismael Ghazzay, Ameel F. Al Shawi, Haitham Noaman Eyada Al-koubaisy, Fatimah Al-Ani, Maadh Aldouri
Publikováno v:
Journal of Emergency Medicine, Trauma and Acute Care. 2022
Autor:
Aytug Kizilors, Roberto Passera, Maadh Aldouri, Christopher Pocock, Syed A Mian, Robin M. Ireland, Jamal Anwar, Antonio Pagliuca, Emily Bart-Smith, Franck E. Nicolini, Elena Crisà, Patrick Harrington, Steve Best, Austin G. Kulasekararaj, Tim Corbett, Ghulam J. Mufti, Clare Wykes, Simon Weston-Smith, Donal P. McLornan, Sophie E. Jackson, Richard Gale, Nicholas Lea, Kavita Raj, Hugues de Lavallade
Publikováno v:
The Lancet Haematology. 6:e276-e284
Kinase domain mutations in BCR-ABL1 are associated with resistance to tyrosine kinase inhibitors in patients with chronic myeloid leukaemia. Next-generation sequencing (NGS) allows detection of low-level kinase domain mutations, but its relevance in
Autor:
Fran Percival, Patrick Chu, Sabine Gaugris, Adrian Lambourne, Maadh Aldouri, John Quinn, Kwee Yong, Martin J. Auger, Supratik Basu
Publikováno v:
European Journal of Cancer Care. 20:697-699
Autor:
David Anthony Ducker, Maadh Aldouri, Aung Soe, Tanoj Gopalam Kollamparambil, Bhavdeep Rameshchandra Jani
Publikováno v:
Acta Paediatrica. 94:499-501
UNLABELLED C(w) is a low frequency red cell antigen that belongs to the Rh blood groups system. While not uncommon, anti-C(w) is rarely associated with clinically significant haemolytic disease of the newborn (HDN). When it does occur, it is often su
Autor:
Hugues de Lavallade, Nicholas Lea, Clare Wykes, Timothy Corbett, Simon Weston-Smith, Mian Syed, Antonio Pagliuca, Aytug Kizilors, Donal P. McLornan, Christopher Pocock, Richard Gale, Maadh Aldouri, Emily Bart-Smith, Elena Crisà, Steven Best, Ghulam J. Mufti, Robin M. Ireland
Publikováno v:
Blood. 126:347-347
Kinase domain (KD) mutations in the BCR-ABL1 gene are associated with resistance to tyrosine kinase inhibitors (TKI) in chronic myeloid leukemia (CML). Next-generation Sequencing (NGS) allows detection of low-level KD mutations but its relevance in c
Autor:
John, Quinn, Fran, Percival, Martin, Auger, Supratik, Basu, Patrick, Chu, Maadh, Aldouri, Adrian, Lambourne, Sabine, Gaugris, Kwee, Yong
Publikováno v:
European journal of cancer care. 20(5)
Autor:
Tanoj Gopalam, Kollamparambil, Bhavdeep Rameshchandra, Jani, Maadh, Aldouri, Aung, Soe, David Anthony, Ducker
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 94(4)
C(w) is a low frequency red cell antigen that belongs to the Rh blood groups system. While not uncommon, anti-C(w) is rarely associated with clinically significant haemolytic disease of the newborn (HDN). When it does occur, it is often subclinical o
Autor:
Maadh Aldouri
Publikováno v:
Pathophysiology of haemostasis and thrombosis. 32
Recombinant factor VIIa (rFVIIa, NovoSeven®) is effective and appears safe in the management of bleeding episodes and provision of surgical cover in haemophilia patients with inhibitors. Additionally, rFVIIa has been considered as a universal haemos
Autor:
A Fensom, Antonio Pagliuca, Maadh Aldouri, ZiYi Lim, Aloysius Ho, Sharon Abrahams, Christopher Shaw, Ghulam J. Mufti
Publikováno v:
Bone Marrow Transplantation. 41:831-832
Sustained neurological improvement following reduced-intensity conditioning allogeneic haematopoietic stem cell transplantation for late-onset Krabbe disease
Autor:
Harold R. Roberts, Maadh Aldouri
Publikováno v:
Transfusion Alternatives in Transfusion Medicine. 5:i-ii