Zobrazeno 1 - 10
of 116
pro vyhledávání: '"Chronic anaemia"'
Publikováno v:
Vox Sanguinis, 117(4), 526-534. WILEY
Background and Objectives: Limited data are available to guide physicians on how to determine the red blood cell (RBC) transfusion regimen in chronically transfusion-dependent patients. The lack of clarity on thresholds and targets to be used for tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eae5197206433b4b7cbb15ac7cc02a54
https://hdl.handle.net/1887/3566429
https://hdl.handle.net/1887/3566429
Autor:
Stephane Fournier, Stephan Windecker, François Mach, Nicolas Rodondi, Thomas F. Lüscher, Christian M. Matter, Thabo Mahendiran, Lorenz Räber, Baris Gencer, David Nanchen, David Meier, Roland Klingenberg, Olivier Muller, David Carballo
Publikováno v:
Journal of Cardiovascular Translational Research. 13:618-628
Discharge anaemia is common following acute coronary syndromes (ACS). However, it is unknown if chronic anaemia (CA) and hospital-acquired anaemia (HAA) are associated with similar outcomes. In this retrospective analysis of 4083 ACS admissions treat
Autor:
Mahasen Al Harbi, Sean R. Bennett
Publikováno v:
Surgery (Oxford). 37:424-430
Both red blood cell (RBC) transfusion and anaemia or low haematocrit increase morbidity and mortality associated with surgery. Chronic anaemia in the elective patient carries a small risk in non-haemorrhagic surgery. Where bleeding is anticipated ana
Bilateral Optic Atrophy in a Young Patient With Chronic Anaemia Secondary to End-Stage Renal Disease
Publikováno v:
Cureus
End-stage renal disease (ESRD) is associated with a number of serious complications, including increased cardiovascular disease, anaemia and metabolic bone disease. Optic atrophy secondary to chronic anaemia in ESRD is rare. We report a case of bilat
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Autor:
Uzoamaka Vivian Muoneke, Emmanuel Anayo Onoh, Ekenechukwu Esther Young, Brenda Chidinma Nwatu
Publikováno v:
PAMJ Clinical Medicine, Vol 3, Iss 190 (2020)
INTRODUCTION: Sickle cell disease is a genetic disorder of haemoglobin characterized by chronic anaemia due to ongoing haemolysis and is frequently associated with recurrent vaso-occlusive crisis (VOC). The affected patients often have impaired immun
Publikováno v:
Перинатологія і педіатрія; № 2(74) (2018): Перинатологія та педіатрія; 13-18
Перинатология и педиатрия; № 2(74) (2018): Перинатология и педиатрия; 13-18
Perinatologiya i pediatriya; No. 2(74) (2018): Perinatologiya i pediatriya; 13-18
Perinatologiâ i Pediatriâ, Iss 2(74), Pp 13-18 (2018)
Перинатология и педиатрия; № 2(74) (2018): Перинатология и педиатрия; 13-18
Perinatologiya i pediatriya; No. 2(74) (2018): Perinatologiya i pediatriya; 13-18
Perinatologiâ i Pediatriâ, Iss 2(74), Pp 13-18 (2018)
Objective: to investigate fetoplacental system in women in II and III trimesters of pregnancy with chronic diseases (anaemia + pyelonephritis) complicated by placental dysfunction; to evaluate the efficiency of ongoing therapy for placental dysfuncti
Autor:
Dejan Urlep, Rajko Kavalar
Publikováno v:
Zdravniški Vestnik, Vol 75, Iss 0 (2006)
Background: Gastric antral vascular ectasia (GAVE), or »watermelon stomach« is a rare but important cause of gastrointestinal blood loss and anaemia, and has characteristic endoscopic and histological features. The pathogenesis of this condition re
Externí odkaz:
https://doaj.org/article/56bfde930a434db4b365286af67e975e
Autor:
Marta Vecchi, G.E. Tontini, Paolo Cantù, Aurora Giannetti, Flaminia Cavallaro, Lorenzo Dioscoridi, Francesco Pugliese, Luca Elli, Alessandro Rimondi, Luca Pastorelli, M. Mutignani
Publikováno v:
Digestive and Liver Disease. 53:S94
Publikováno v:
Acta Haematologica Polonica. 48:35-39
Background Chronic anaemia mainly thalassemia and sickle cell anaemia are inherited disorders of haemoglobin. Presently about 7% of the world's populations are carriers of a potentially pathological haemoglobin gene. Sickle cell disease is a common h