Translation of "Hemolytic anemia" in German

Hemolytic anemia is-- well, it's when the red blood cells rupture and become dysfunctional.

So it's a genetic defect just like hemolytic anemia.

The causes of hemolytic anemia vary and may be inherited or acquired.

Hemolytic anemia is characterized by increased levels of indirect bilirubin in the bloodstream.

Hemolytic anemia can be developed after several courses of cisplatin.

Hereditary spherocytosis is the most frequent hereditary hemolytic anemia in central europe.

Biological differential diagnoses include other non-autoimmune causes of hemolytic anemia.

Recessive type of hemolytic anemia in childrenIt is much greater than the dominant.

But the situation in case of illnessnesferotsitarnymi forms of hemolytic anemia is much more difficult.

This is why this disease is also known as immune-mediated hemolytic anemia, or IMHA.

Common symptoms are corneal opacities, hemolytic anemia, and xanthoma cells in the bone marrow.

In isolated cases, patients with prolonged use of this drug may experience leukopenia, bone marrow damage, or hemolytic anemia.

Few rare, isolated cases of thrombocytopenia, leukopenia and hemolytic anemia are described in the literature.

Hemolytic anemia is treated with antibiotics and medicines, slowing the destruction of red blood cells.

Patients presented with thrombocytopenia, microangiopathic hemolytic anemia, and acute kidney injury, without severe deficiencies in ADAMTS13 activity.

Researchers (including at my laboratory) have investigated how the body naturally handles the occasional release of hemoglobin from aging red blood cells and from cells affected by blood diseases, such as hemolytic anemia.

High doses of 5 g/kg placed on the skin of cats cause death through hemolytic anemia.

Mm. I was trying to figure out why this patient's having seizures when I noticed she has a hemolytic anemia.

The features of graft-versus-host disease, which is based on an immune reaction originating from the transplant and directed against the host tissue, are, in the form having an acute course which almost always ends fatally, enlargement of the spleen, hepatomegaly, lymph node hypertrophy, hemolytic anemia, low immunoglobulin and complement levels, and diminished immunoreactivity.

In homozygotes, nearly all Hb is in the HbC form, resulting in mild hemolytic anemia.

Among them, six patients developed hemolytic anemia week after treatment possibily related to artesunate or had persistent signs of hemolytic activity until six weeks after the first dose of iv artesunate.

However, fortunately, including hemolytic anemia is most common dominant type of disease, called anemia, Chauffard Minkowski.

Hemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia (see this term) characterized by pronounced microcytic hypochromic hemolytic anemia.

Removal of the spleen is of little assistance in patients with IgM-mediated hemolytic disorders, but may be helpful in those with therapy-resistant IgG-mediated hemolytic anemia.