Zobrazeno 1 - 10
of 189
pro vyhledávání: '"Haemolytic anaemias"'
Autor:
Rachel Kesse-Adu, Jo Howard
Publikováno v:
Medicine. 49:210-216
Inherited haemolytic anaemias are caused by a genetic mutation that results in an abnormality within the red cell leading to its early destruction. This abnormality can affect the cell membrane (e.g. hereditary spherocytosis), result from an absence
Autor:
Vassilios Voudris, Apostolos Armaganidis, Anastasia Anthi, Panagiotis Karyofyllis, Dimitrios Tsiapras, Stylianos E. Orfanos
Publikováno v:
Pulmonary Circulation, Vol 11 (2021)
Pulmonary Circulation
Pulmonary Circulation
Pulmonary hypertension (PH) development remains a significant cardiovascular complication of haemoglobinopathies, severely affecting the morbidity and mortality of such patients. According to the 5th World Symposium on PH, PH related with chronic hae
Autor:
Richard G. Jenner, Roger G. Owen, Lydia Eccersley, Laura Clifton-Hadley, Rakesh Popat, William R. Wilson, Elizabeth H Phillips, Selina J Chavda, Kwee Yong, Marie Scully, Michael Sheaff, Matthew Streetly, Gavin Pang, Karthik Ramasamy, Ceri Bygrave, Andres Virchis, James D. Cavenagh, Jonathan Sive, Gordon Cook, Sumaiya Kamora, Marquita Camilleri, Maria José Cuadrado, Michael A Chapman, Reuben Benjamin
Publikováno v:
Phillips, E 2021, ' Thrombotic microangiopathy in untreated myeloma patients receiving carfilzomib, cyclophosphamide and dexamethasone on the CARDAMON study. ', British Journal of Haematology, vol. 193, no. 4, pp. 750-760 . https://doi.org/10.1111/bjh.17377
Proteasome inhibitors have been associated with thrombotic microangiopathy (TMA) - a group of disorders characterised by occlusive microvascular thrombosis causing microangiopathic haemolytic anaemia, thrombocytopenia and end-organ damage. To date, c
Autor:
Paola Bianchi, Johannes G. G. Dobbe, Geert J. Streekstra, Martijn Veldthuis, Elisa Fermo, Timothy J. Satchwell, Rob van Zwieten, Richard van Wijk, Ashley M. Toye, Pedro L. Moura, Minke A.E. Rab
Publikováno v:
Moura, P L, Dobbe, J G G, Streekstra, G J, Rab, M A E, Veldthuis, M, Fermo, E, van Wijk, R, van Zwieten, R, Bianchi, P, Toye, A M & Satchwell, T 2020, ' Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning ', British Journal of Haematology . https://doi.org/10.1111/bjh.16868
British Journal of Haematology
British journal of haematology, 190(4), e250-e255. Wiley-Blackwell
British Journal of Haematology
British journal of haematology, 190(4), e250-e255. Wiley-Blackwell
[No Abstract]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d344171cde2dcc73acdf99b40b353a48
https://research-information.bris.ac.uk/en/publications/4533f96b-a5dd-434f-84a7-bf2eddb9d5f7
https://research-information.bris.ac.uk/en/publications/4533f96b-a5dd-434f-84a7-bf2eddb9d5f7
Autor:
Donald R. Branch
Publikováno v:
ISBT Science Series. 14:49-52
Publikováno v:
Annals of Pathology and Laboratory Medicine. 5:A283-288
Background: Anaemia is a major public health problem in developing countries like India. Kavaratti island, Lakshadweep is a remote island located in Arabian sea. There is extreme paucity of data on the type of anaemia here. Objective of this study is
Publikováno v:
Asian Journal of Transfusion Science
Direct Antiglobulin Test is a method of demonstrating the presence of antibody/ complement bound to red cell membrane by using AHG to form a visible agglutination reaction. DAT positivity is seen in immune mediated haemolytic anaemias, however rarely
Autor:
Abdulgabar Salama
Publikováno v:
Transfusion Medicine and Hemotherapy
Autoimmune haemolytic anaemias (AIHAs) are well-characterized disorders. They can be differentiated from one another and from other non-immune haemolytic anaemias by clinical, laboratory and serological testing. However, several misleading clinical p
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