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T-follicular helper cell expansion and chronic T-cell activation are characteristic immune anomalies in Evans syndrome

open access: yesBlood, 2021
Evans syndrome (ES) is the co-occurrence of autoimmune hemolytic anemia and immune thrombocytopenia. Kumar et al investigated the immune profile of 24 pediatric patients with ES in comparison to 22 ITP patients and 24 healthy controls, analysing ...
Deepak Kumar   +20 more
semanticscholar   +1 more source

New-onset Evans syndrome associated with systemic lupus erythematosus after BNT162b2 mRNA COVID-19 vaccination

open access: yesInternational journal of hematology, 2021
Evans syndrome presents as concurrent autoimmune hemolytic anemia (AIHA) and immune thrombocytopenia (ITP). Systemic lupus erythematosus (SLE) is the most frequent autoimmune disorder associated with Evans syndrome.
Daisuke Hidaka   +11 more
semanticscholar   +1 more source

Evans syndrome and its link with systemic lupus erythematosus

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2016
Evans syndrome is a rare syndrome associated with the presence of autoimmune hemolytic anemia and simultaneous or sequential development of thrombocytopenia. It was first described by Evan and Duane in 1951.
Satish Mendonca   +5 more
doaj   +1 more source

Long term follow-up of pediatric-onset Evans syndrome: broad immunopathological manifestations and high treatment burden

open access: yesHaematologica, 2021
Pediatric-onset Evans syndrome (pES) is defined by both immune thrombocytopenic purpura (ITP) and autoimmune hemolytic anemia (AIHA) before the age of 18 years.
T. Pincez   +30 more
semanticscholar   +1 more source

ADEM post-Sars-CoV-2 infection in a pediatric patient with Fisher-Evans syndrome

open access: yesNeurological Sciences, 2021
Sars-CoV-2 is a single-strained RNA virus belonging to Coronaviridae’s family. In pediatric age, the majority of patients is asymptomatic; however, several neurological manifestations associated with Sars-CoV-2 infection have been detected in a ...
M. L. Manzo   +7 more
semanticscholar   +1 more source

Evans syndrome: A rare cause of persistent thrombocytopenia in children

open access: yesJournal of Pediatric Critical Care, 2015
Background: Evans syndrome is characterized by simultaneous or sequential development of autoimmune thrombocytopenia (AITP) and autoimmune hemolytic anemia (AIHA).
Kanchan Channawar, V S V Prasad
doaj   +1 more source

Evans Syndrome Presenting as an Atypical Complication of SARS-CoV-2 Vaccination

open access: yesCureus, 2022
The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has drastically affected our daily lives, causing millions of deaths worldwide.
M. De Felice   +4 more
semanticscholar   +1 more source

The co-occurrence of multiple sclerosis and Evans syndrome: A case report

open access: yesCaspian Journal of Internal Medicine, 2020
Background: Evans syndrome is an uncommon autoimmune disorder manifested by fatigue, jaundice, pallor, purpura and petechiae. The main characteristics of this rare disease are simultaneous or sequential existence of positive anti-globulin test, immune ...
Mohammad Ali Sahraian   +2 more
doaj  

Alveolar hemorrhage linked to Evans syndrome

open access: yesEgyptian Journal of Chest Disease and Tuberculosis, 2022
Evans syndrome associates thrombocytopenia, autoimmune hemolytic anemia, and/or neutropenia with a positive direct antihuman globulin test. It is an autoimmune entity.
Nidhal Belloumi   +5 more
doaj   +1 more source

Are there “Attenuated” Forms of Evans Syndrome? [PDF]

open access: yesHematology, 2001
Indirect evidence of hemolysis has been described in patients with autoimmune thrombocytopenic purpura. In order to collect more data, another method to assess red blood cell destruction in these patients was employed: measurement of free haptoglobin levels. In 17 individuals with autoimmune thrombocytopenic purpura the levels of free haptoglobins were
G J, Ruiz-Argüelles   +4 more
openaire   +2 more sources

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