Results 61 to 70 of about 375,109 (185)
Journal of Family Medicine and Primary Care, 2015 The array of diagnostic workup for pyrexia of unknown origin (PUO) generally revolves in searching for infections, inflammatory/autoimmune, and endocrine etiologies.
Vikas A Mishra +2 more
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A case of asymptomatic pancytopenia with clinical features of hemolysis as a presentation of pernicious anemia [PDF]
Journal of Community Hospital Internal Medicine Perspectives, 2016 Pernicious anemia is an autoimmune disease with a variety of clinical presentations. We describe a case of pernicious anemia presenting with pancytopenia with hemolytic features.
Venkateswara K. Kollipara +3 more
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Hemolytic anemia due to native valve subacute endocarditis with Actinomyces israelii infection
Clinical Case Reports, 2018 This case highlights the importance of considering infectious etiology in the management of hemolytic anemia. Hemolytic anemia associated with infectious endocarditis is rare.
S. Toom, Yiqing Xu
semanticscholar +1 more source
Warm antibody autoimmune hemolytic anemia.
Hematology. American Society of Hematology. Education Program, 2016 Autoimmune hemolytic anemia (AIHA) is a rare and heterogeneous disease that affects 1 to 3/100 000 patients per year. AIHA caused by warm autoantibodies (w-AIHA), ie, antibodies that react with their antigens on the red blood cell optimally at 37°C, is ...
T. Kalfa
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Tegsedi-Induced Warm Antibody Autoimmune Hemolytic Anemia
Annals of Internal Medicine: Clinical CasesAutoimmune hemolytic anemia is a hemolytic disorder in which antibodies attack erythrocytes, causing their destruction. Many medications have been linked to autoimmune hemolytic anemia, such as antibiotics, chemotherapy agents, and nonsteroidal anti ...
Mariela Di Vanna +3 more
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Anemia hemolítica autoimune e colite ulcerosa.
Acta Médica Portuguesa, 1995 Although several associations of autoimmune disorders with ulcerative colitis have been reported, autoimmune hemolytic anemia is extremely rare. We report a case of a 35 year-old white woman with a twelve-year history of mild ulcerative colitis treated ...
L Rebocho, M Lucas, R M Victorino
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Diagnostic approaches for inherited hemolytic anemia in the genetic era
Blood Research, 2017 Inherited hemolytic anemias (IHAs) are genetic diseases that present with anemia due to the increased destruction of circulating abnormal RBCs. The RBC abnormalities are classified into the three major disorders of membranopathies, hemoglobinopathies ...
Yonggoo Kim +2 more
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Toxins, 2020 The global emergence of clinical diseases caused by enterohemorrhagic Escherichia coli (EHEC) is an issue of great concern. EHEC release Shiga toxins (Stxs) as their key virulence factors, and investigations on the cell-damaging mechanisms toward target ...
Johanna Detzner +2 more
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Microangiopathic Hemolytic Anemia and Thrombocytopenia in Patients With Cancer.
Journal of Oncology Practice, 2016 The unexpected occurrence of thrombotic microangiopathy (TMA), characterized by microangiopathic hemolytic anemia and thrombocytopenia, in a patient with cancer requires urgent diagnosis and appropriate management. TMA is a term used to describe multiple
Jordan Morton, J. George
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Mediterranean Journal of Hematology and Infectious Diseases, 2014 Summary: Hemolytic anemia is a collection of diseases resulting from an exaggeration of the lysis of red blood cells. Hemolysis can be caused by extravacular aggression by drugs or other toxic or by antibodies againt red blood cell.
JAMILA ELHOUDZI
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