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	1.	Hereditary spherocytosis is more frequent than expected: what to tell the patient? [electronic resource] by Kutter, Dolphe Producer: 20050923 In: Bulletin de la Societe des sciences medicales du Grand-Duche de Luxembourg no. 1 Availability: No items available. Save to lists Add to cart (remove)
	2.	Demonstration and quantification of "hyperchromic" erythrocytes by haematological analysers. Application to screening for hereditary and acquired spherocytosis. [electronic resource] by Kutter, Dolphe Coulon, Nathalie Stirn, Fernand Thoma, Martine Janecki, Jerzy Producer: 20030711 In: Clinical laboratory vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	3.	Growing significance of myeloperoxidase in non-infectious diseases. [electronic resource] by Hoy, Aline Leininger-Muller, Brigitte Kutter, Dolphe Siest, Gérard Visvikis, Sophie Producer: 20020927 In: Clinical chemistry and laboratory medicine vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	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. [electronic resource] by Mauch, Lysann Lun, Andreas O'Gorman, Maurice R G Harris, John S Schulze, Ilka Zychlinsky, Arturo Fuchs, Tobias Oelschlägel, Uta Brenner, Sebastian Kutter, Dolphe Rösen-Wolff, Angela Roesler, Joachim Producer: 20070612 In: Clinical chemistry vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)