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Clinical characteristics and outcome of patients with autoimmune hemolytic anemia (AIHA) uniformly defined as primary by a diagnostic work-up

Title: Clinical characteristics and outcome of patients with autoimmune hemolytic anemia (AIHA) uniformly defined as primary by a diagnostic work-up
Authors: MAURO, Francesca Romana; Coluzzi, S; Paoloni, F; Trastulli, F; ARMIENTO, DANIELE; FERRETTI, ANTONIETTA; GIOVANNETTI, GIANLUCA; COLAFIGLI, GIOIA; MOLICA, MATTEO; LA ROCCA, URSULA; De Propris, Ms; CARONNA, Roberto; Morano, G; GUARINI, Anna; GIRELLI, Gabriella; FOA, Roberto
Contributors: Mauro, Francesca Romana; Coluzzi, S; Paoloni, F; Trastulli, F; Armiento, Daniele; Ferretti, Antonietta; Giovannetti, Gianluca; Colafigli, Gioia; Molica, Matteo; LA ROCCA, Ursula; De Propris, M; Caronna, Roberto; Morano, G; Guarini, Anna; Girelli, Gabriella; Foa, Roberto
Publisher Information: John Wiley & Sons, Inc.; Hoboken, NJ
Publication Year: 2016
Collection: Sapienza Università di Roma: CINECA IRIS
Subject Terms: Autoimmune hemolytic anemia
Description: Primary autoimmune hemolytic anemia (P-AIHA) is a relatively uncommon and hetereogeneous disease characterized by the destruction of red blood cells due to anti-erythrocyte autoantibodies (AeAbs) in the absence of an associated disease [1–3]. Secondary AHIA is frequently associated with lymphoproliferative diseases (LD) in particular, chronic lymphocytic leukemia, aggressive or indolent lymphomas, autoimmune disorders, malignancies other than lymphoid, and infections [1,2,4]. On the hypothetical assumption that in a significant proportion of cases defined as P-AIHA the clinical heterogeneity could be due to an ignored associated disease, we retrospectively analyzed the clinical characteristics and outcome of patients with a diagnosis of P-AIHA based on a diagnostic work-up aimed at excluding or identifying an associated disease. .
Document Type: article in journal/newspaper
File Description: ELETTRONICO
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/27059006; info:eu-repo/semantics/altIdentifier/wos/WOS:000380261900002; volume:91; issue:7; firstpage:E319; lastpage:E320; numberofpages:2; journal:AMERICAN JOURNAL OF HEMATOLOGY; http://hdl.handle.net/11573/868549
DOI: 10.1002/ajh.24379
Availability: http://hdl.handle.net/11573/868549; https://doi.org/10.1002/ajh.24379
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.22D6C466
Database: BASE