Publications by authors named "Dolphe Kutter"

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Chronic granulomatous disease (CGD) and complete myeloperoxidase deficiency both yield strongly reduced dihydrorhodamine 123 test signals but can be easily discerned in routine testing for CGD.
Lysann Mauch, Andreas Lun, Maurice R G O'Gorman, John S Harris, Ilka Schulze, Dolphe Kutter

Clin Chem· May 2007

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Hereditary spherocytosis is more frequent than expected: what to tell the patient?
Dolphe Kutter

Bull Soc Sci Med Grand Duche Luxemb· September 2005

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Demonstration and quantification of "hyperchromic" erythrocytes by haematological analysers. Application to screening for hereditary and acquired spherocytosis.
Dolphe Kutter, Nathalie Coulon, Fernand Stirn, Martine Thoma, Jerzy Janecki

Clin Lab· July 2003

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Growing significance of myeloperoxidase in non-infectious diseases.
Aline Hoy, Brigitte Leininger-Muller, Dolphe Kutter, Gérard Siest, Sophie Visvikis

Clin Chem Lab Med· January 2002

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