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Silvia Escribano Serrat: Flow Cytometric Osmotic Fragility Testing for Diagnosis of Hereditary Spherocytosis
May 14, 2026, 16:06

Silvia Escribano Serrat: Flow Cytometric Osmotic Fragility Testing for Diagnosis of Hereditary Spherocytosis

Silvia Escribano Serrat, Research Fellow at Memorial Sloan Kettering Cancer Center, shared a post on LinkedIn about a recent article she and her colleagues co-authored, published in Cytometry Part B: Clinical Cytometry։

”I’m pleased to share our article published in Cytometry Part B: Clinical Cytometry, focused on the evaluation of flow cytometric osmotic fragility testing for the diagnosis of hereditary spherocytosis.

This study was carried out during my time at Hospital Clínic de Barcelona, in the Hemostasis and Erythropathology Laboratory. We assessed the performance of this method in a clinical laboratory setting and its usefulness as part of the diagnostic workflow for red blood cell membrane disorders.

I would like to thank Maribel Diaz-Ricart, Meritxell Nomdedeu Fàbrega, and, especially, the excellent team of technicians for their support and collaboration throughout the study.”

Title: Diagnostic performance of flow cytometric osmotic fragility testing in hereditary spherocytosis

Authors: Silvia Escribano Serrat, Patricia Molina, Pilar Gómez, Mireia Garre, Meritxell Nomdedeu, Blanca De Moner, Estefanía García, Ana Belén Moreno-Castaño, Álex Ramos, Julia Martinez-Sanchez, Marc Pino, Ginés Escolar, Maribel Díaz-Ricart

Silvia Escribano Serrat: Flow Cytometric Osmotic Fragility Testing for Diagnosis of Hereditary Spherocytosis

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