with aplastic crisis. Six of these patients had sickle cell anemia, the seventh patient had beta thalassemia intermedia. Virologic studies showed that six patients had acute infection with the human parvovirus-like virus; in the remaining patient the lack of appropriate specimens precluded viral diagnosis. We describe the features of the virus infection and accompanying erythroid aplasia, and discuss the role of parvovirus-like virus as the etiologic agent in the arrest of erythrocyte production. TRANSIENT ARREST of erythropoiesis with rapidly wors-ening anemia is well described in patients with chronic hemolytic disease including sickle cell anemia and heredi-tary spherocytosis (1, 2). In most of these patients, no etiologic agent can be i...
In patients with chronic congenital haemolytic disorders, human Parvovirus B19 (HPV B19) is frequent...
Differential diagnosis for anemia late after allogeneic stem cell transplantation is broad. In this ...
Splenic dysfunction is a major feature of sickle cell disease (SCD) and can manifest as acute spleni...
Human parvovirus B19 (PV-B19) causes erythema infectiosum, hydrops fetalis, and transient aplastic c...
Human Parvovirus infection is associated with transient aplastic crisis as a most common complicatio...
In our Paediatric Clinic we observed a case of transient aplastic crisis caused by Parvovirus B19 in...
The association between aplastic crisis and human parvovirus (HPV) B19 infection has been described ...
Acute parvovirus B19 infection may lead to erythroblastopenia crisis in patients with underlying red...
Parvovirus B19 infection in pediatrics most commonly causes fifth disease, a mild viral illness. Hem...
The association between aplastic crisis and human parvovirus (HPV) B19 infection is well described i...
Aplastic phase serum from a patient with aplastic crisis of hereditary spherocytosis, which was demo...
Human parvovirus B19has been associated with disease only for the past few years. First isolated fro...
Healthy adult volunteers were inoculated intranasally with human parvovirus obtained from an asympto...
Human parvovirus (HPV) B19 induced aplastic crisis in a family leading to the diagnosis of hereditar...
Background: Human parvovirus B19 (HPV-B19) is the etiologic agent of erythema infectiosum, of transi...
In patients with chronic congenital haemolytic disorders, human Parvovirus B19 (HPV B19) is frequent...
Differential diagnosis for anemia late after allogeneic stem cell transplantation is broad. In this ...
Splenic dysfunction is a major feature of sickle cell disease (SCD) and can manifest as acute spleni...
Human parvovirus B19 (PV-B19) causes erythema infectiosum, hydrops fetalis, and transient aplastic c...
Human Parvovirus infection is associated with transient aplastic crisis as a most common complicatio...
In our Paediatric Clinic we observed a case of transient aplastic crisis caused by Parvovirus B19 in...
The association between aplastic crisis and human parvovirus (HPV) B19 infection has been described ...
Acute parvovirus B19 infection may lead to erythroblastopenia crisis in patients with underlying red...
Parvovirus B19 infection in pediatrics most commonly causes fifth disease, a mild viral illness. Hem...
The association between aplastic crisis and human parvovirus (HPV) B19 infection is well described i...
Aplastic phase serum from a patient with aplastic crisis of hereditary spherocytosis, which was demo...
Human parvovirus B19has been associated with disease only for the past few years. First isolated fro...
Healthy adult volunteers were inoculated intranasally with human parvovirus obtained from an asympto...
Human parvovirus (HPV) B19 induced aplastic crisis in a family leading to the diagnosis of hereditar...
Background: Human parvovirus B19 (HPV-B19) is the etiologic agent of erythema infectiosum, of transi...
In patients with chronic congenital haemolytic disorders, human Parvovirus B19 (HPV B19) is frequent...
Differential diagnosis for anemia late after allogeneic stem cell transplantation is broad. In this ...
Splenic dysfunction is a major feature of sickle cell disease (SCD) and can manifest as acute spleni...