Results 101 to 110 of about 65,576 (316)
Journal of clinical apheresis, 2020 We performed a systematic review and meta‐analysis to evaluate the efficacy and safety of therapeutic plasma exchange (TPE) in adult patients with autoimmune hemolytic anemia (AIHA).
Jiawen Deng +4 more
semanticscholar +1 more source
Comorbidities in aging patients with sickle cell disease. [PDF]
, 2018 Sickle cell disease (SCD) in general and sickle cell anemia in particular is a highly complex disorder both at the molecular and clinical levels. Although the molecular lesion is a single-point mutation, the sickle gene is pleiotropic in nature causing ...
Ballas, Samir K.
core +2 more sources
Difficult Cases of Autoimmune Hemolytic Anemia: A Challenge for the Internal Medicine Specialist
Journal of Clinical Medicine, 2020 Autoimmune hemolytic anemia (AIHA) is diagnosed in the presence of anemia, hemolysis, and direct antiglobulin test (DAT) positivity with monospecific antisera. Many confounders of anemia and hemolytic markers should be included in the initial workup (i.e.
B. Fattizzo +3 more
semanticscholar +1 more source
Opportunities and Challenges of Population Pharmacogenomics
Annals of Human Genetics, EarlyView.ABSTRACT Pharmacological responses can vary significantly among patients from different ethnogeographic backgrounds. This variability can, at least in part, be attributed to population‐specific genetic patterns in genes involved in drug absorption, distribution, metabolism, and excretion, as well as in genes associated with drug‐induced toxicity ...
Yitian Zhou +3 more
wiley +1 more source
Hereditary hemochromatosis associated with autoimmune hemolytic anemia; A case report [PDF]
Journal of Preventive Epidemiology, 2019 Hereditary hemochromatosis is a disease associated with highly iron overload. This disease caused by genetic mutations inherited through family. Autoimmune hemolytic anemia is also an important autoimmune disease in which red blood cells (RBC) are ...
Masih Falahatian +2 more
doaj
Rheumatoid Arthritis and Autoimmune Hemolytic Anemia as First Manifestation of Rhupus
Case Reports in Rheumatology, 2020 “Rhupus” syndrome is a rare condition that describes the coexistence of systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA), which prevalence among patients with SLE varies from 0.01% to 9.7%.
Alejandra Espinosa-Orantes +4 more
doaj +1 more source
Allergy, EarlyView.T cell receptor repertoire analysis by high‐throughput immune repertoire RNA‐sequencing in the patients with DOCK8 deficiency. Comprehensive comparisons revealed a restricted TCR repertoire diversity in the patients. Additional assessments showed potential auto‐reactive CD8+ T cell clones in the patients.Abbreviations: DOCK8, dedicator of cytokinesis ...
Ceren Bozkurt +26 more
wiley +1 more source
Haematologica, 2011 Background Autoimmune hemolytic anemia is a rare condition in children. Little is known about its initial presentation and the subsequent progression of the disease.Design and Methods Since 2004, a national observational study has been aiming to ...
Nathalie Aladjidi +19 more
doaj +1 more source
Anemia hemolítica secundaria a timoma sin miastenia gravis como síndrome paratímico: Presentación de un caso [PDF]
, 2016 Describimos el caso de un paciente masculino de 41 años que cursa con cuadro clínico de dolor torácico, astenia y adinamia, con estudios imagenológicos que evidencian masa en mediastino anterior que corresponde a timoma, de acuerdo con el reporte de ...
Hurtado Amézquita, Camilo +3 more
core +1 more source
British Journal of Haematology, EarlyView.Follicular lymphoma (FL), marginal zone lymphoma (MZL), chronic lymphocytic leukaemia (CLL) and mantle cell lymphoma (MCL) are characterized by a continuous incidence of relapse and increasing resistance to therapy. Novel immunotherapy approaches are needed.
Rahul Lakhotia +11 more
wiley +1 more source