Showing 1 - 3 results of 3 for search 'L. Kager', 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
    P1046: SEVERE COMPLICATIONS IN JAK2 V617F POSITIVE PEDIATRIC PATIENTS WITH MYELOPROLIFERATIVE NEOPLASMS

    P1046: SEVERE COMPLICATIONS IN JAK2 V617F POSITIVE PEDIATRIC PATIENTS WITH MYELOPROLIFERATIVE NEOPLASMS by W. Novak, C. Annamária, R. Crazzolara, J. Neil, K. Pirolt, M. Dworzak, L. Kager

    Published 2022-06-01
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  3. 3
    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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