Results 101 to 110 of about 236,446 (302)
TRIM Expression and Its Association With Disease Activity in Systemic Lupus Erythematosus
ABSTRACT Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with diverse manifestations, including rash, arthritis, and nephritis. Although autoantibodies are a key feature of SLE, their levels often poorly reflect disease severity, suggesting the involvement of additional contributing factors.
Ling‐Ying Lu +8 more
wiley +1 more source
Proton pump inhibitors induce hemolytic anemia
Proton pump inhibitors (PPIs) are generally safe, and their short-term use commonly does not induce hemolytic anemia. The underlying mechanisms are unknown, and the literature insufficiently explores hemolytic anemia as an adverse event induced by PPIs ...
Asayil Nasser Al-Nasser +2 more
core +1 more source
Acute hemolysis in association with hepatitis B infection in a child with beta-thalassemia trait
Autoimmune hemolytic anemia may occur in the course of some viral diseases such as Coxsackie virus, cytomegalovirus, Epstein Barr virus, Influenza A, herpes simplex virus, and rarely hepatitis B virus infection.
A Gürgey, A Yüce, N Ozbek, N Koçak
doaj
ABSTRACT Objective SURMOUNT‐REAL UK will evaluate the effectiveness of tirzepatide when offered in addition to standard‐of‐care (SoC) in adults with Class I obesity (BMI ≥ 30 and ≤ 34.9 kg/m2) and without diabetes in a UK primary care setting. Methods A 5‐year, phase 4, multicenter, open‐label, pragmatic randomized clinical trial is enabled through ...
Martin K. Rutter +14 more
wiley +1 more source
Lupus Anticoagulant Positivity as a Risk Marker for Hemolytic Anemia in Patients with APS
Background and Objectives: Thrombocytopenia and hemolytic anemia are common but non-criteria manifestations of antiphospholipid syndrome (APS). However, their relationship with specific immunological profiles remains poorly characterized.
Ji-Hyoun Kang
doaj +1 more source
ABSTRACT Aim In this article, we present two cases of severe fetal hemolytic anemia based on a beta‐thalassaemia trait inherited from a single parent. Results These cases, presented at 20 and 28 weeks' gestation, necessitated intra‐uterine blood transfusions.
Eva van der Meij +11 more
wiley +1 more source
[[abstract]]INTRODUCTION: Unlike autoimmune hemolytic anemia (AIHA), literature on the etiological study of non-autoimmune hemolytic anemia (non-AIHA) is scarce. The incidence and prevalence of non-AIHA in different geographic regions are largely unknown
Victor C Kok;郭集慶;Chien-Kuan Lee;Jorng-Tzong Horng;洪炯宗;Che-Chen Lin;Fung-Chang Sung
core
Laboratory evaluation of hemolytic anemia [PDF]
Author of a master‘s thesis. Dalia Vertelytė The title of the master‘s thesis. Laboratory evaluation of hemolytic anemia. The aim: To evaluate changes of laboratory tests during hemolytic anemia and relate them with of type of hemolytic anemia ...
Vertelytė, Dalia
core
ABSTRACT Prenatal exome sequencing (ES) can establish rare genetic diagnoses in a fetus but may also lead to occult genetic diagnosis in a biological parent. We present a case of dual fetal and maternal diagnosis by prenatal ES, in a fetus with unexplained anemia and in a pregnant patient with sickle cell disease (SCD) and recurrent unexplained hypoxia.
Matthew A. Shear +6 more
wiley +1 more source

