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Browsing by Author Riepe, F.G.
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| Full Text | Issue Date | Title | Author(s) | | 2006 | Absence of exercise-induced leptin suppression associated with insufficient epinephrine reserve in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency. | Riepe, F.G.; Krone, N.; Kruger, S.N.; Sweep, C.G.J.; Lenders, J.W.M., et al |
| 2005 | Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations. | Vallette-Kasic, S.; Brue, T.; Pulichino, A.M.; Gueydan, M.; Barlier, A., et al |
| 2004 | Congenital isolated ACTH deficiency, an underestimated cause of neonatal death, explained by TPIT mutations | Vallette-Kasic, S.; Brue, T.; Pulichino, A.M.; Gueydan, M.; Barlier, A., et al |
Showing results 1 to 3 of 3
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