Results 111 to 120 of about 9,026 (213)
Clinical and Translational Discovery, Volume 6, Issue 5, October 2026.Sickle cell disease inflammation emerges from interconnected cytokine networks. Immune‐informatics integrates multi‐omics, network biology and artificial intelligence to decode inflammatory signatures, predict complications and identify precision therapeutic targets. Abstract Background Sickle cell disease (SCD) is characterised by chronic inflammation
Emmanuel Ifeanyi Obeagu +1 more
wiley +1 more source
Evaluating Reproductive Health Recommendations in CPGs for Sickle Cell Disease: An Umbrella Review
Clinical and Public Health Guidelines, Volume 3, Issue 4, October 2026.ABSTRACT Background Individuals with sickle cell disease or trait (SCD/T) face significant reproductive health risks, highlighting the need to assess the best available evidence on their reproductive health needs. Objectives To assess the quality of SCD/T clinical practice guidelines and evaluate the key characteristics and quality of their ...
Lisa R. Roberts +4 more
wiley +1 more source
Evaluation of four hemoglobin separation analyzers for hemoglobinopathy diagnosis
, 2017 BackgroundFour automated hemoglobin separation devices are compared in their ability to detect hemoglobinopathies, both in HbA1c and in hemoglobinopathy mode.
Rémy Coens +11 more
core +1 more source
EHA Guidelines on the management of children and adults with hemoglobin SC disease
HemaSphere, Volume 10, Issue 10, October 2026.Abstract HbSC disease is the second most common type of sickle cell disease (SCD) in populations of African origin. Although it is often grouped together with other types of SCD, particularly sickle cell anemia (HbSS), it has unique pathophysiology and a different spectrum of laboratory and clinical features.
David C. Rees +15 more
wiley +1 more source
Premarital hemoglobinopathy screening in Kocaeli, Turkey: a crowded industrial center on the north coast of Marmara Sea [PDF]
, 2009 Objective: Premarital hemoglobinopathy screening is one of the important procedures of hemoglobinopathy control programs. This is the first report about the prevalence of hemoglobinopathies in Kocaeli.
Özcan Şahin +4 more
core +1 more source
, 2013 Background: Co-inheritance of hemoglobin gene defects is a rare important status that can lead to double heterozygote or homozygote with significant clinical manifestations. Such conditions can be observed in co-inheritance of alpha-thalassemia with beta-
Fakher Rahim +8 more
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, 2014 Background: Hemoglobinopathy is inherited anemia characterized by abnormal structure of one of the globin chains of the hemoglobin molecule and has been known to be rare in Korea.
박, 준은 +3 more
core +1 more source
Seroprevalence of Hepatitis B, Hepatitis C and HIV in Patients with Hemoglobinopathy Patients
, 2014 Purpose: Thalassemia and sickle cell anemia patients have frequent transfusions. Hepatitis B (HBV), hepatitis C (HCV) and human immunodeficiency virus (HIV) are tramsmitted infections with blood.
Can Acipayam +3 more
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Health Science Reports, Volume 9, Issue 10, October 2026.ABSTRACT Background and Aims Infertility nowadays is considered a disease and a significant global health issue. Despite extensive research, the cause of approximately 15% of infertility cases remains unknown. Additionally, despite the high financial and emotional costs associated with infertility treatment, there is no single universal method that ...
Zeinab Eftekhar +4 more
wiley +1 more source
Tissue oxygenation in patients with hemoglobinopathy H
, 1997 To evaluate the degree of tissue hypoxia in patients with hemoglobinopathy H disease, whole blood oxygen affinity was estimated and analyzed in 33 patients.
Kanavakis, E +3 more
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