Showing 1 - 3 results of 3 for search 'R. Jimenez-Heredia', query time: 0.02s Refine Results
  1. 1
    PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY

    PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY by J. Berner, W. Novak, R. Jimenez-Heredia, L. Kager, K. Boztug

    Published 2022-06-01
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  2. 2
    P1531: HETEROGENEITY OF DISEASE-CAUSING GENOTYPES BETWEEN FAMILIES WITH HEREDITARY SPHEROCYTOSIS: A SINGLE-CENTER COHORT STUDY

    P1531: HETEROGENEITY OF DISEASE-CAUSING GENOTYPES BETWEEN FAMILIES WITH HEREDITARY SPHEROCYTOSIS: A SINGLE-CENTER COHORT STUDY by R. Jimenez Heredia, L. Kager, P. Zeitlhofer, W. Novak, S. Eder, A. Segarra Roca, K. Nebral, M. Haimel, R. Geyeregger, O. Haas, K. Boztug

    Published 2022-06-01
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  3. 3
    P1408: MONOALLELIC AND BIALLELIC GERMLINE MUTATIONS AFFECTING THE TRANSCRIPTION FACTOR HELIOS CAUSE PLEIOTROPIC DEFECTS OF IMMUNITY

    P1408: MONOALLELIC AND BIALLELIC GERMLINE MUTATIONS AFFECTING THE TRANSCRIPTION FACTOR HELIOS CAUSE PLEIOTROPIC DEFECTS OF IMMUNITY by D. Mayr, T. Shahin, M. Shoeb, H. S. Kuehn, B. Hoeger, S. Giuliani, L. Gawriyski, Ö. Yüce Petronczki, J. Hadjadj, S. Köstel Bal, S. Zoghi, M. Haimel, R. Jimenez Heredia, D. Boutboul, M. Triebwasser, F. Rialland-Battisti, S. Tangye, T. Fleisher, N. Rezaei, N. Romberg, S. Latour, M. Varjosalo, F. Halbritter, F. Rieux-Laucat, I. Castanon, S. Rosenzweig, K. Boztug

    Published 2022-06-01
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