Showing 1 - 7 results of 7 for search 'J.L. Vives Corrons', query time: 0.02s Refine Results
  1. 1
    PB2248: CONCOMITANT HEREDITARY SPHEROCYTOSIS AND PYRUVATE KINASE DEFICIENCY IN A SPANISH FAMILY WITH CHRONIC HEMOLYTIC ANEMIA. CONTRIBUTION OF LASER EKTACYTOMETRY TO CLINICAL DIAGNOSIS

    PB2248: CONCOMITANT HEREDITARY SPHEROCYTOSIS AND PYRUVATE KINASE DEFICIENCY IN A SPANISH FAMILY WITH CHRONIC HEMOLYTIC ANEMIA. CONTRIBUTION OF LASER EKTACYTOMETRY TO CLINICAL DIAGN... by J.-L. Vives Corrons, E. Krishnevskaya, L. Montllor, V. Leguizamón, M. Garcia Bernal

    Published 2022-06-01
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  2. 2
    P1550: NEW GENERATION EKTACYTOMETRY STUDY OF RED BLOOD CELLS RHEOLOGICAL PARAMETERS IN HEMOGLOBINOPATHIES

    P1550: NEW GENERATION EKTACYTOMETRY STUDY OF RED BLOOD CELLS RHEOLOGICAL PARAMETERS IN HEMOGLOBINOPATHIES by E. Krishnevskaya, M. Molero Magariño, Á. Ancochea Serra, J.-L. Vives Corrons, I. Hernandez, V. Leguizamón

    Published 2022-06-01
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  3. 3
    P1551: CONFORMATIONAL STUDY OF PYRUVATE KINASE DEFICIENT VARIANTS WITH HEMOLYTIC ANEMIA. THE RELATIONSHIPS BETWEEN THE LOSS OF ENZYME FUNCTION AND STRUCTURAL DISRUPTION

    P1551: CONFORMATIONAL STUDY OF PYRUVATE KINASE DEFICIENT VARIANTS WITH HEMOLYTIC ANEMIA. THE RELATIONSHIPS BETWEEN THE LOSS OF ENZYME FUNCTION AND STRUCTURAL DISRUPTION by L. Jorda, L. Montllor, E. Krisnevskaya, V. Leguizamón, I. Hernandez, J. L. Gelpi, J.-L. Vives Corrons

    Published 2022-06-01
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  4. 4
    Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to γ-glutamylcysteine synthetase deficiency in a patient of Moroccan origin

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

    Published 2007-11-01
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  5. 5
    P1542: COMORBIDITIES AND COMPLICATIONS ACROSS GENOTYPES IN ADULT PATIENTS WITH PYRUVATE KINASE DEFICIENCY: ANALYSIS FROM THE PEAK REGISTRY

    P1542: COMORBIDITIES AND COMPLICATIONS ACROSS GENOTYPES IN ADULT PATIENTS WITH PYRUVATE KINASE DEFICIENCY: ANALYSIS FROM THE PEAK REGISTRY by A. Glenthøj, R. F. Grace, E. J. van Beers, J.-L. Vives Corrons, B. Glader, K. H. M. Kuo, C. Lander, D. Pospíŝilová, J. Williams, Y. Yan, B. McGee, P. Bianchi

    Published 2022-06-01
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  6. 6
    P1562: CHARACTERIZING IRON OVERLOAD BY AGE IN PATIENTS DIAGNOSED WITH PYRUVATE KINASE DEFICIENCY – A DESCRIPTIVE ANALYSIS FROM THE PEAK REGISTRY

    P1562: CHARACTERIZING IRON OVERLOAD BY AGE IN PATIENTS DIAGNOSED WITH PYRUVATE KINASE DEFICIENCY – A DESCRIPTIVE ANALYSIS FROM THE PEAK REGISTRY by P. Bianchi, R. F. Grace, J.-L. Vives Corrons, B. Glader, A. Glenthøj, H. Kanno, K. H. Kuo, C. Lander, D. M. Layton, D. Pospíŝilová, V. Viprakasit, J. Williams, Y. Yan, B. McGee, E. J. van Beers

    Published 2022-06-01
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  7. 7
    CALR ins5-mediated clonal hematopoiesis causes severe hemolytic anemia in a female PGK1 Ser320Asn carrier

    CALR ins5-mediated clonal hematopoiesis causes severe hemolytic anemia in a female PGK1 Ser320Asn carrier by M. L. Morales, H. Cano, B. de la Morena-Barrio, J. L. Vives-Corrons, E. J. Cuenca-Zamora, P. Garrido-Rodríguez, C. Bento, J. Pereira, J. Martínez Nieto, T. H. Chen-Liang, J. L. Fuster, S. Caracena, M. L. Lozano, R. Teruel-Montoya, J. Corral, F. Ferrer-Marín

    Published 2025-02-01
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