P793: SCREENING OF NATURALLY OCCURRING CXCR4 VARIANTS FOR IDENTIFICATION OF NOVEL PATHOGENIC MUTATIONS FOR WHIM SYNDROME
Pawar, S., Wiest, I., Maier-Munsa, S., Maierhofer, B., Sondheimer, N., Taveras, A. G., Badarau, A., Zmajkovicova, K.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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PRELIMINARY CLINICAL DATA FROM A PHASE 1B STUDY OF MAVORIXAFOR AND IBRUTINIB IN PATIENTS WITH WALDENSTRöM MACROGLOBULINEMIA WITH MYD88 AND CXCR4 MUTATIONS
Treon, S., Buske, C., Thomas, S., Branagan, A., Dimopoulos, M., Castillo, J. J., Garzon, F., Tang, W., Ronan, R., Seyffert, S., Garg, V., Ali, S., Taveras, A., Badarau, A., Zmajkovicova, K., Maier, S., Maierhofer, B., Matous, J.
Published in Hematological oncology (01.06.2021)
Published in Hematological oncology (01.06.2021)
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P1253: MAVORIXAFOR DISRUPTS THE CROSS TALK BETWEEN WALDENSTRÖM'S MACROGLOBULINEMIA CELLS AND THE BONE MARROW MICROENVIRONMENT RESULTING IN ENHANCED SENSITIVITY TO B‐CELL TARGETED THERAPIES
Monticelli, H., Kruitwagen, T., Tardelli, M., Rebelo, T., Maierhofer, B., Maier‐Munsa, S., Zmajkovicova, K., Taveras, A. G., Nguyen, C.
Published in HemaSphere (23.06.2022)
Published in HemaSphere (23.06.2022)
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Osteogenesis imperfecta in childhood: cardiac and renal manifestations
Vetter, U, Maierhofer, B, Müller, M, Lang, D, Teller, W M, Brenner, R, Frohneberg, D, Wörsdörfer, O
Published in European journal of pediatrics (01.12.1989)
Published in European journal of pediatrics (01.12.1989)
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Journal Article
P793: SCREENING OF NATURALLY OCCURRING CXCR4 VARIANTS FOR IDENTIFICATION OF NOVEL PATHOGENIC MUTATIONS FOR WHIM SYNDROME
Pawar, S., Wiest, I., Maier‐Munsa, S., Maierhofer, B., Sondheimer, N., Taveras, A. G., Badarau, A., Zmajkovicova, K.
Published in HemaSphere (01.06.2022)
Published in HemaSphere (01.06.2022)
Get full text
Journal Article