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1 Ergebnisse
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A serious and unusual presentation of congenital isolated A..:
Vieira, Inês Henriques
;
Mourinho Bala, Nádia
;
Ramos, Fabiana
...
Endocrinology, Diabetes & Metabolism Case Reports. 2022 (2022) - p. , 2022
Link:
https://doi.org/10.1530/edm-22-0277
RT Journal T1
A serious and unusual presentation of congenital isolated ACTH deficiency due to TBX19 mutation, beyond the neonatal period
UL https://suche.suub.uni-bremen.de/peid=cr-10.1530_edm-22-0277&Exemplar=1&LAN=DE A1 Vieira, Inês Henriques A1 Mourinho Bala, Nádia A1 Ramos, Fabiana A1 Dinis, Isabel A1 Cardoso, Rita A1 Caetano, Joana Serra A1 Rodrigues, Dírcea A1 Paiva, Isabel A1 Mirante, Alice PB Bioscientifica YR 2022 SN 2052-0573 JF Endocrinology, Diabetes & Metabolism Case Reports VO 2022 LK http://dx.doi.org/https://doi.org/10.1530/edm-22-0277 DO https://doi.org/10.1530/edm-22-0277 SF ELIB - SuUB Bremen
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