A case report described an infant with concurrent HDFN and SMA who was succesfully treated with an onasemnogene abeparvovec ...

Hemolysis was diagnosed by anemia (hemoglobin level below 14 g/dL), reticulocytosis ... Neonatal management and outcome in alloimmune hemolytic disease. Expert Rev Hematol. 2017;10(7):607-16. Epub ...

This paper demonstrates a previously undescribed defect of a glycolytic enzyme, triosephosphate isomerase, in the erythrocytes and leukocytes of a patient with congenital hemolytic anemia.

Four cases of Coombs-positive hemolytic anemia have been described in which the administration of penicillin to patients with circulating antipenicillin antibody was the suspected cause of the ...

the alloimmune diseases of pregnancy. So with FcRn blockade, you therefore have the ability to selectively target one of the underlying causes of myasthenia gravis: by reducing from circulation ...

in association with profound anemia. The patient was transfusion-dependent, with evidence of impaired erthyropoiesis. Treatment with four doses of rituximab was followed by an increase in his EPO ...

Bone-marrow-derived multipotent progenitor stromal cells — or mesenchymal stem cells (MSCs) — are the common predecessors of cells of the mesenchymal lineage, such as bone, cartilage and fat ...

This unique case underscores the importance of meticulous prenatal and postnatal immunologic workup when alloimmune conditions are suspected. Clinicians should consider the possibility of dual ...

A 2-week-old child who presented with petechiae was found to have a very low platelet count and was diagnosed with fetal and neonatal alloimmune thrombocytopenia (FNAIT). This case report was ...

Background Hemolytic disease of the fetus and newborn is a public health problem caused by maternal-fetal incompatibility; no prophylaxis is available for most alloantibodies that induce this disease.

TMEM63B-related developmental and epileptic encephalopathy with anemia (MONDO:0800503) childhood-onset self-limited focal epilepsy syndrome (MONDO:0800502) palmoplantar hyperkeratosis, DSG1-related, ...