Results 111 to 120 of about 1,197,543 (390)
Anemia, 2012 Fanconi anemia (FA) is a rare inherited disease characterized by developmental defects, short stature, bone marrow failure, and a high risk of malignancies. FA is heterogeneous: 15 genetic subtypes have been distinguished so far.
Johan J. P. Gille +5 more
doaj +1 more source
THE TREATMENT OF ANEMIA. [PDF]
Journal of the American Medical Association, 1907 I do not intend to read a paper on the details of the treatment of anemia. All are familiar with the chief measures and remedies employed in this treatment: Iron, arsenic, rest, nutrition, fresh air and other dietary and hygienic measures. As to the particulars, any of the many good text-books will give the desired information.
openaire +3 more sources
American Journal of Hematology, EarlyView.Mixed autoimmune hemolytic anemia (AIHA) is a rare condition characterized by the presence of both warm and cold autoantibodies, often leading to severe, treatment‐resistant hemolysis. In this systematic review of 81 patients across 35 studies, the median age was 45 years with a notable female predominance.
Jeremy W. Jacobs +12 more
wiley +1 more source
Prevalence of Iron Deficiency Anemia among University Students in Hodeida Province, Yemen
Anemia, 2018 Background. Iron deficiency anemia (IDA) is one of the most common types of nutritional anemia in the worldwide and considered a major public health problem in developing countries especially in Yemen.
Abdullah Ahmed Al-alimi +2 more
doaj +1 more source
Vitamin A Supplementation and Other Predictors of Anemia Among Children from Dar Es Salaam, Tanzania. [PDF]
, 2000 The associations of hemoglobin, hematocrit, and packed cell volume with socioeconomic factors, malaria, human immunodeficiency virus (HIV) infection, and nutritional status were examined among 687 children admitted to hospital with pneumonia ...
Fawzi, W W +4 more
core +1 more source
American Journal of Hematology, EarlyView.ABSTRACT We analyzed 193 Fanconi anemia patients from the Italian Registry, focusing on hematological outcome, cancer risk, and mortality, both in transplanted (n = 130, 67.4% of the cohort) and non‐transplanted (n = 63, 36.6% of the cohort) patients. After a median follow‐up of 7 years, almost all patients developed cytopenia that was more frequent in
Erica Ricci +35 more
wiley +1 more source
Anemia, 2012 Sickle cell anemia is one of the best studied inherited diseases, and despite being caused by a single point mutation in the HBB gene, multiple pleiotropic effects of the abnormal hemoglobin S production range from vaso-occlusive crisis, stroke, and ...
Mário Angelo Claudino +1 more
doaj +1 more source
Hypoxia-Inducible Factor Activators in Renal Anemia: Current Clinical Experience.
Advances in Chronic Kidney Disease, 2019 Prolyl hydroxylase domain oxygen sensors are dioxygenases that regulate the activity of hypoxia-inducible factor (HIF), which controls renal and hepatic erythropoietin production and coordinates erythropoiesis with iron metabolism.
Neil S. Sanghani, V. Haase
semanticscholar +1 more source
Prenatal Brain Abnormalities in Sodium‐Dependent Multivitamin Transporter Deficiency
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT In treatable neurometabolic disorders, early diagnosis and prompt initiation of treatment are key to improved survival and outcomes. Biallelic variants in SLC5A6 cause sodium‐dependent multivitamin transporter deficiency (OMIM # 618973), which is treatable with high‐dose pantothenic acid, biotin, and alpha lipoic acid.
Eri Ogawa +2 more
wiley +1 more source
Anemia, 2012 Introduction. Patients with β-thalassemia intermedia have a higher incidence of thromboembolic events compared to the general population. Previous studies have shown that patients with sickle cell disease, who are also prone to ischemic events, have ...
Nahid Ashjazadeh +4 more
doaj +1 more source