Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders by Llaudet‐Planas, E., Vives‐Corrons, J. L., Rizzuto, V., Gómez‐Ramírez, P., Sevilla Navarro, J., Coll Sibina, M. T., García‐Bernal, M., Ruiz Llobet, A., Badell, I., Velasco‐Puyó, P., Dapena, J. L., Mañú‐Pereira, M. M.

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O‐02: RADIOMICS AND ARTIFICIAL INTELLIGENCE FOR IDENTIFICATION AND MONITORING OF SILENT CEREBRAL INFARCTS IN SICKLE CELL DISEASE: FIRST ANALYSIS FROM THE GENOMED4ALL EUROPEAN PROJE... by R., BIONDI, M., BOARO, N., BIONDINI, A., COLLADO GIMBERT, J., ESCUDERO FERNANDEZ, V., PINTO, N., ROMANO, V., VOI, G., FERRERO, M., CASALE, M., CIRILLO, G., PALAZZI, F., CAVALLERI, G., FORNI, G., REGGIANI, S., PERROTTA, M., MANU PEREIRA, S., ZAZO, K., MARIAS, M., DE MONTALEMBERT, P., BARTOLUCCI, E., VANBEERS, F., ALVAREZ, F., CREMONESI, T., SANAVIA, P., FARISELLI, G., CASTELLANI, R., MANARA, R., COLOMBATTI

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S265: RADIOMICS AND ARTIFICIAL INTELLIGENCE FOR IDENTIFICATION AND MONITORING OF SILENT CEREBRAL INFARCTS IN SICKLE CELL DISEASE: FIRST ANALYSIS FROM THE GENOMED4ALL EUROPEAN PROJE... by Boaro, M. P., Biondi, R., Biondini, N., Collado Gimbert, A., JM, E. F., Pinto, V., Romano, N., Voi, V., Ferrero, G. B., Casale, M., Cirillo, M., Palazzi, G., Cavalleri, F., Forni, G. L., Reggiani, G., Perrotta, S., Manu Pereira, M., Zazo, S., Marias, K., De Montalembert, M., Bartolucci, P., Beers, E., Alvarez, F., Cremonesi, F., Sanavia, T., Fariselli, P., Castellani, G., Manara, R., Colombatti, R.

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PB2352: CONSOLIDATION OF ERN‐EUROBLOODNET: THE EUROPEAN REFERENCE NETWORK ON RARE HEMATOLOGICAL DISEASES FIRST 5 YEARS OF IMPLEMENTATION by Mañú Pereira, M. D. M., Gutierrez Valle, V., Pellegrini, M., Rodríguez Sánchez, M. D. L. Á., Margot, L., Gulbis, B., Fenaux, P.

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P1478: INTEGRATIVE DIAGNOSIS OF SICKLE CELL DISEASE PATIENTS FOR PERSONALIZED MEDICINE by Idrizovic, A., Collado Gimbert, A., Beers, E., Colombatti, R., Bartolucci, P., Montalembert, M., Boaro, M. P., Beneitez, D., Ortuño, A., Ruiz, A., Isola, I., Cela, E., Van Wijk, R., Rab, M., Mañú Pereira, M. D. M.

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P1481: THE INTERNATIONAL HEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HEMOGLOBINOPATHIES by Kountouris, P., Stephanou, C., Archer, N., Bonifazi, F., Giannuzzi, V., Kuo, K., Maggio, A., Makani, J., Mañú Pereira, M. D. M., Michailidou, K., Nkya, S. W., Nnodu, O., Trompeter, S., Tshilolo, L., Wonkam, A., Zilfalil, B. A., Inusa, B., Kleanthous, M.

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Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin by Mañú Pereira, M, Gelbart, T, Ristoff, E, Crain, K C, Bergua, J M, López Lafuente, A, Kalko, S G, García Mateos, E, Beutler, E, Vives Corrons, J L

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P‐023: 2,3‐DIPHOSPHOGLYCERATE DETECTION VIA DIRECT INFUSION HIGH RESOLUTION MASS SPECTROMETRY CORRELATES WITH QUANTITATIVE DETECTION IN BLOOD OF PATIENTS WITH SICKLE CELL DISEASE... by S., VAN DER VEEN, M., VAN DIJK, J., JANS, N., VERHOEVEN‐DUIF, R., VAN WIJK, M., BARTELS, M., MAÑÚ PEREIRA, R., COLOMBATTI, M., MARTELLA, V., MUNARETO, M., BOARO, P., BARTOLLUCI, M., CNOSSEN, B., BIEMOND, E., VAN BEERS

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Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to {gamma}-glutamylcysteine synthetase deficiency in a patient of Moroccan origin by Manu Pereira, M, Gelbart, T, Ristoff, E, Crain, K.C, Bergua, J.M, Lopez Lafuente, A, Kalko, S.G, Garcia Mateos, E, Beutler, E, Vives Corrons, J.L

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P‐032: INTEGRATIVE DIAGNOSIS OF SICKLE CELL DISEASE PATIENTS FOR PERSONALIZED MEDICINE by A., IDRIZOVIC, A., COLLADO GIMBERT, E., VAN BEERS, R., COLOMBATTI, P., BARTOLUCCI, M., DE MONTALEMBERT, M., BOARO, D., BENEITEZ, A., ORTUÑO, A., RUIZ, I., ISOLA, E., CELA, R., VAN WIJK, M., RAB, M., MAÑU PEREIRA

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PI‐07: THE INTERNATIONAL HEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HEMOGLOBINOPATHIES by P., KOUNTOURIS, C., STEPHANOU, N., ARCHER, F., BONIFAZI, V., GIANNUZZI, K., KUO, A., MAGGIO, J., MAKANI, M., MAÑÚ PEREIRA, K., MICHAILIDOU, S., NKYA, O., NNODU, S., TROMPETER, L., TSHILOLO, A., WONKAM, B., ZILFALIL, B., INUSA, M., KLEANTHOUS

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P1500: 2,3‐DIPHOSPHOGLYCERATE DETECTION VIA DIRECT INFUSION HIGH RESOLUTION MASS SPECTROMETRY CORRELATES WITH QUANTITATIVE DETECTION IN BLOOD OF PATIENTS WITH SICKLE CELL DISEASE by Veen, S., Dijk, M., Jans, J., Verhoeven‐Duif, N., Wijk, R., Bartels, M., Mañú Pereira, M., Colombatti, R., Martella, M., Munaretto, V., Boaro, M., Bartolucci, P., Cnossen, M., Biemond, B., Beers, E.

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New e-health services for the European Network for Rare and Congenital Anaemias (e-ENERCA) by Vives Corrons, J L, Maéú Pereira, M, Olaya, L

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P117: THE INTERNATIONAL HAEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HAEMOGLOBINOPATHIES by Kountouris, P, Stephanou, C, Archer, N, Bonifazi, F, Giannuzzi, V, Kuo, K, Maggio, A, Makani, J, Mañú Pereira, M, Michailidou, K, Nkya, S, Nnodu, O, Trompeter, S, Tshilolo, L, Wonkam, A, Zilfalil, B, Inusa, B, Kleanthous, M

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S283: ERN-EUROBLOODNET EUROPEAN REGISTRY OF PATIENTS AFFECTED BY RED BLOOD CELL DISORDERS AND COVID-19 by Velasco, P., Longo, F., Piolatto, A., Bardón-Cancho, E. J., Ponce-Salas, B., Flevari, P., Voskaridou, E., Biemond, B. J., Nur, E, Delaporta, P., Besse-Hammer, T., Ruiz-Llobet, A., Raso, S., Spasiano, A., Guerzoni, M. E., Beneitez-Pastor, D., Dedeken, L., Pepe, A., Rosso, R., Kunz, J. B., de Montalembert, M., Campisi, S., Glenthøj, A., Gonzalez Urdiales, P., Benghiat, F. S., Azerad, M.-A., Saunders, C. J., Ferreira Faria, T., Casini, T., Bagnato, S., Van de Velde, A., Labarque, V., Bertoni, E., Van Damme, A., Diamantidis, M. D., Russo, R., Stiakaki, E., Quota, A, Christou, S., Teles, M. J., Lafiatis, I., Kerkhoffs, J.-L., Argüello Marina, M., Lorite, M., Rodriguez, A., Iolascon, A., Taher, A. T., Colombatti, R., Roy, N., Mañú Pereira, M. D. M.

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Haemoglobin Köln as a cause of haemolytic anaemia and splenomegaly by Durán Urdániz, G, Gil Sáenz, F J, Molina Garicano, J, Gimeno Ballester, J, Mañú Pereira, M M

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P117: THE INTERNATIONAL HAEMOGLOBINOPATHY RESEARCH NETWORK (INHERENT): AN INTERNATIONAL INITIATIVE TO STUDY THE ROLE OF GENETIC MODIFIERS IN HAEMOGLOBINOPATHIES by Kountouris, P, Stephanou, C, Archer, N, Bonifazi, F, Giannuzzi, V, Kuo, K, Maggio, A, Makani, J, Mañú Pereira, M, Michailidou, K, Nkya, S, Nnodu, O, Trompeter, S, Tshilolo, L, Wonkam, A, Zilfalil, B, Inusa, B, Kleanthous, M

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Hemoglobina de Köln como causa de anemia hemolítica y esplenomegalia by Durán Urdániz, G, Gil Sáenz, F.J, Molina Garicano, J, Gimeno Ballester, J, Mañú Pereira, M.M

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PS1196 INNOVATIVE DIAGNOSTIC APPROACH FOR RARE ANEMIA by Rizzuto, V., Álvarez, A. Blanco, Vega, B. Tazón, Pastor, D. Beneitez, Pereira, M.D. M. Mañú

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S283: ERN‐EUROBLOODNET EUROPEAN REGISTRY OF PATIENTS AFFECTED BY RED BLOOD CELL DISORDERS AND COVID‐19 by Velasco, P., Longo, F., Piolatto, A., Bardón‐Cancho, E. J., Ponce‐Salas, B., Flevari, P., Voskaridou, E., Biemond, B. J., Nur, E, Delaporta, P., Besse‐Hammer, T., Ruiz‐Llobet, A., Raso, S., Spasiano, A., Guerzoni, M. E., Beneitez‐Pastor, D., Dedeken, L., Pepe, A., Rosso, R., Kunz, J. B., Montalembert, M., Campisi, S., Glenthøj, A., Gonzalez Urdiales, P., Benghiat, F. S., Azerad, M.‐A., Saunders, C. J., Ferreira Faria, T., Casini, T., Bagnato, S., Van de Velde, A., Labarque, V., Bertoni, E., Van Damme, A., Diamantidis, M. D., Russo, R., Stiakaki, E., Quota, A, Christou, S., Teles, M. J., Lafiatis, I., Kerkhoffs, J.‐L., Argüello Marina, M., Lorite, M., Rodriguez, A., Iolascon, A., Taher, A. T., Colombatti, R., Roy, N., Mañú Pereira, M. D. M.

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