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- W2011521208 abstract "A presentation is made of a patient with myelofibrosis and chronic haemolytic anaemia. Known causes of haemolysis in combination with myelofibrosis were excluded. A hereditary red cell glucose-6-phosphate dehydrogenase (G-6-PD) deficiency was found. The case history is reported, along with the results of haematological investigations in the affected members of the family. Emphasis is laid on the opinion that not only red cell sequestration in the spleen and a PNH-like syndrome must be taken into account, but also G-6-PD deficiency, particularly when haemolytic episodes occur in combination with bacterial infections in patients with myelofibrosis." @default.
- W2011521208 created "2016-06-24" @default.
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- W2011521208 date "2009-04-24" @default.
- W2011521208 modified "2023-09-26" @default.
- W2011521208 title "Glucose-6-Phosphate Dehydrogenase Deficiency and Myelofibrosis" @default.
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- W2011521208 doi "https://doi.org/10.1111/j.1600-0609.1973.tb00103.x" @default.
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