Results 41 to 50 of about 14,704 (250)
Ironing out the details: Untangling dietary iron and genetic background in diabetes [PDF]
, 2018 The search for genetic risk factors in type-II diabetes has been hindered by a failure to consider dietary variables. Dietary nutrients impact metabolic disease risk and severity and are essential to maintaining metabolic health.
Lawson, Heather A, Miranda, Mario A
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, 2015 The bottom line Clarify the warfarin dose that the patient is taking, and check for co-existing problems (such as liver disease or cancer), dietary changes, and intake of alcohol and other drugs that may increase risk of bleeding or affect ...
Chevassut, Timothy J +2 more
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USO TERAPÊUTICO DE SANGRIAS: UMA REVISÃO DE LITERATURA
Hematology, Transfusion and Cell Therapy, 2021 Objetivos: A flebotomia terapêutica é um método de retirada de sangue, de modo a tratar e prevenir diversas condições tóxicas para o organismo.
ALM Lopes, JSI Chaves, JPL Cezar
doaj +1 more source
Indications and Contraindications of Phlebotomy According to Avicenna in Al-Qanun fi al-Tibb (The Canon of Medicine) [PDF]
Journal of Research on History of MedicineToday, phlebotomy has a limited application in modern medicine and is prescribed for only a few specific conditions. However, recent studies have explored its potential effectiveness in treating a broader range of diseases. As phlebotomy has historically
Shahram Homayounkeshi +1 more
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Biomarkers of Inflammation and Fibrosis in Kawasaki Disease Patients Years After Initial Presentation With Low Ejection Fraction. [PDF]
, 2020 Background Coronary artery aneurysms and myocarditis are well-recognized complications of Kawasaki disease (KD) but no systematic evaluation of the consequences of myocarditis has been performed in the subset presenting with low ejection fraction (EF ...
Burns, Jane C +5 more
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Biomarkers for Huntington's disease: an update [PDF]
, 2012 Huntington's disease (HD) is a devastating autosomal-dominant neurodegenerative condition caused by a CAG repeat expansion in the gene encoding huntingtin which is characterised by progressive motor impairment, cognitive decline and neuropsychiatric ...
Scahill, RI, Tabrizi, SJ, Wild, EJ
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Orphanet Journal of Rare Diseases, 2020 Background Aceruloplasminemia is a rare genetic iron overload disorder, characterized by progressive neurological manifestations. The effects of iron chelation on neurological outcomes have only been described in case studies, and are inconsistent ...
Lena H. P. Vroegindeweij +3 more
doaj +1 more source
Molecular Genetics and Metabolism Reports, 2021 Congenital erythropoietic porphyria (CEP) is an autosomal recessive disorder of the heme biosynthetic pathway that is characterized by uroporphyrinogen III synthase (UROS) deficiency and the accumulation of non-physiological isomer I porphyrins.
Jean-Marc Blouin +10 more
doaj +1 more source
Microfluidic flow chambers using reconstituted blood to model hemostasis and platelet transfusion in vitro [PDF]
, 2016 Blood platelets prepared for transfusion gradually lose hemostatic function during storage. Platelet function can be investigated using a variety of (indirect) in vitro experiments, but none of these is as comprehensive as microfluidic flow chambers.
Compernolle, Veerle +4 more
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Macrophages support pathological erythropoiesis in Polycythemia Vera and Beta-Thalassemia [PDF]
, 2014 Regulation of erythropoiesis is achieved by integration of distinct signals. Among these, macrophages are emerging as erythropoietin-complementary regulators of erythroid development, particularly under stress conditions. We investigated the contribution
Abdel-Wahab, Omar +15 more
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