Results 51 to 60 of about 375,109 (185)

The Prevalence of Peripheral Erythrophagocytosis in Pediatric Immune-Mediated Hemolytic Anemia. [PDF]

open access: yesHematol Rep
Background: Peripheral erythrophagocytosis appears to be a unique sign of acquired immune-mediated hemolytic anemia. It is said to be rare but its prevalence among patients with autoimmune hemolytic anemia has not been studied.
Lee AC.
europepmc   +2 more sources

Essential thrombocythemia, hemolytic anemia and hepatic cirrhosis: Could there be an association?

open access: yesHematology Reports, 2018
Vascular events are the most common clinical complication of essential thrombocythemia, leading to sign and symptoms of this disease. There are various sign and symptoms of essential thrombocythemia, such as thrombosis in artery or vein, and enlarged ...
Nata Pratama Hardjo Lugito   +4 more
doaj   +1 more source

Daratumumab in life-threatening autoimmune hemolytic anemia following hematopoietic stem cell transplantation.

open access: yesBlood Advances, 2018
New-onset autoimmune hemolytic anemia (AIHA) occurs in 2% to 6% of pediatric patients post-hematopoietic stem cell transplantation (HSCT) and is a significant complication.
C. Schuetz   +9 more
semanticscholar   +1 more source

The challenge of microangiopathic hemolytic anemia

open access: yesIraqi Journal of Hematology, 2017
Microangiopathic hemolytic anemia (MAHA) is a Coomb's-negative hemolytic anemia characterized by red cell fragmentation (schistocytes). Thrombotic microangiopathy anemia, including thrombotic thrombocytopenia and hemolytic-uremic syndrome, malignant ...
Hassanain Hani Hassan   +1 more
doaj   +1 more source

Positive predictive value of diagnosis coding for hemolytic anemias in the Danish National Patient Register

open access: yesClinical Epidemiology, 2016
Dennis Lund Hansen,1 Ulrik Malthe Overgaard,2 Lars Pedersen,3 Henrik Frederiksen1,3 1Department of Haematology, Odense University Hospital, Odense, 2Department of Haematology, Herlev Hospital, Herlev, 3Department of Clinical Epidemiology, Aarhus ...
Hansen DL   +3 more
doaj  

Inherited hemolytic anemia: a possessive beginner's guide.

open access: yesHematology. American Society of Hematology. Education Program, 2018
Significant advances have been made in diagnosis and clinical management of inherited red cell membrane disorders that result in hemolytic anemia.
N. Mohandas
semanticscholar   +1 more source

Impairment of bone health in pediatric patients with hemolytic anemia. [PDF]

open access: yesPLoS ONE, 2014
INTRODUCTION: Sickle cell anemia and thalassemia result in impaired bone health in both adults and youths. Children with other types of chronic hemolytic anemia may also display impaired bone health.
Michael M Schündeln   +8 more
doaj   +1 more source

Infantile Cytomegalovirus-Associated Severe Warm Autoimmune Hemolytic Anemia: A Case Report

open access: yesChildren, 2017
Autoimmune hemolytic anemia is a rare hematologic entity in children. Etiologies are mainly viruses or bacteria. We describe here a case of severe warm autoimmune hemolytic anemia (IgG- and C3d-positive direct antiglobulin test) in an immunocompetent 6 ...
Hassan K. Khalifeh   +2 more
doaj   +1 more source

Problem of the diagnosis of acquired hemolytic anemia in childhood

open access: yesZdorovʹe Rebenka, 2020
Autoimmune hemolytic anemia is a heterogeneous group of diseases that are associated with decompensated acquired hemolysis. Autoimmune hemolytic anemia in children is most commonly observed after a viral illness. However, it is quite a rare disorder with
S.O. Nykytyuk   +4 more
doaj   +1 more source

How I treat autoimmune hemolytic anemia.

open access: yesBlood, 2017
Autoimmune hemolytic anemia (AIHA) is an uncommon entity that presents diagnostic, prognostic, and therapeutic dilemmas despite being a well-recognized entity for over 150 years.
R. Go, J. Winters, N. Kay
semanticscholar   +1 more source

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