Results 91 to 100 of about 400,917 (195)

Hematologic disorders in systemic lupus erythematosus

Acta Médica del Centro, 2010
A total of 194 cases of patients suffering from systemic lupus erythematosus were reviewed. The hematologic disorders that appeared in the classification criteria were: autoimmune hemolytic anemia (Coombs-positive) in 14 patients (7%), leukopenia in 38 ...
José Francisco Martínez Delgado, Marta Pérez de Alejo Rodríguez, Julio Horaldo López-Silverio Moya   +2 more
doaj  

Red Cell Lipids in Autoimmune Hemolytic Anemia [PDF]

, 1969
V Brabec, Č Michalec, J Palek, M Kout
openalex   +1 more source

THE LIPID AND MINERAL DISTRIBUTION OF THE SERUM AND ERYTHROCYTES IN THE HEMOLYTIC AND HYPOCHROMIC ANEMIAS OF CHILDHOOD

, 1937
Betty Nims Erickson, Harold H. Williams, Frances Cope Hummel, Pearl Lee, Icie G. Macy   +4 more
openalex   +1 more source

57 Autoimmune Hemolytic Anemia in a Patient with Congenital Hypogammaglobulinemia [PDF]

, 1967
Howard A. Pearson, John B. Robbins, Richard G. Skinner   +2 more
openalex   +1 more source

Respiratory Syncytial Virus Vaccine Induced Thrombotic Microangiopathy

Journal of Blood Medicine
Robert Seby,1 Benjamin J McCormick,1 Emily Wolf,2 Justin Kuhlman,2 Nikita Jhawar,1 Sven Peter Oman,1 Adam M Kase,2 Chancey Christenson,3 Marwan Shaikh2 1Department of Internal Medicine, Mayo Clinic, Jacksonville, FL, USA; 2Department of Hematology ...
Seby R, McCormick BJ, Wolf E, Kuhlman J, Jhawar N, Oman SP, Kase AM, Christenson C, Shaikh M   +8 more
doaj  

Autoimmune hemolytic anemia as presenting manifestation of primary splenic anaplastic large cell lymphoma

The Turkish Journal of Pediatrics, 2006
Autoimmune hemolytic anemia (AIHA) is an unusual complication of malignancy. We diagnosed primary splenic anaplastic large cell lymphoma (ALCL) in a patient. A seven-year-old boy presented with Coombs test-positive hemolytic anemia. After a course
Yavuz Köksal, Umran Calişkan, Canan Uçar, Selim Erekul, Zeynep Ilerisoy Yakut   +4 more
doaj  

Gilbert syndrome in patients with inherited hemolytic anemia modifies the clinical phenotype

Pediatric Hematology Oncology Journal
Gilbert syndrome is a benign condition due to UGT1A1 mutations frequently resulting in mild, indirect hyperbilirubinemia. Inherited hemolytic anemias often present with hyperbilirubinemia and hepatosplenomegaly.
Anika Agrawal, Jagdish Chandra
doaj   +1 more source

Brief Report: Erythropoiesis after Exchange Transfusion in Hemolytic Anemia [PDF]

, 1966
Allan J. Erslev, Joseph P. McKenna
openalex   +1 more source

Diagnosis and treatment of autoimmune hemolytic anemia in adults: Recommendations from the First International Consensus Meeting.

Blood reviews, 2019
U. Jäger, W. Barcellini, C. Broome, M. Gertz, A. Hill, Q. Hill, B. Jilma, D. Kuter, M. Michel, M. Montillo, A. Röth, S. Zeerleder, S. Berentsen   +12 more
semanticscholar   +1 more source

Pathogenesis of Hemolytic Anemia in Homozygous Hemoglobin C Disease* [PDF]

, 1967
Samuel Charache, C. Lockard Conley, David F. Waugh, Richard J. Ugoretz, J. Richard Spurrell   +4 more
openalex   +1 more source