Severe primary IGF1 deficiency diagnosed by a standardized IGF1/IGFBP3 generation test : the belgian experience

Ryckx, S.;Derycke, C.;Anckaert, E.;Beauloye, V.;De Schepper, J.;et.al.
(2022) European Society for Pediatric Endocrinology — Location: Rome (15.September.2022)

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Ryckx, S., Derycke, C., Anckaert, E., Beauloye, V., Beckers, D., Brachet C., Den Bricker, M., De Waele, K., Dotremont, H., Boros, E., Klink, D., Lebrethon, M. C., Lysy, P., Mouraux, T., Parent A.S., vander Straaten, S., Rochtus, A., & De Schepper, J. (2022). Severe primary IGF1 deficiency diagnosed by a standardized IGF1/IGFBP3 generation test : the belgian experience. European Society for Pediatric Endocrinology, Rome. https://hdl.handle.net/2078.5/164693