Amélie Besson

GH mutant (R77C) in a pedigree presenting with the delay of growth and pubertal development: structural analysis of the mutant and evaluation of the biological activity.

M. Thevis, C. Flück, P. Mullis, 2007, European journal of endocrinology.

Short stature caused by a biologically inactive mutant growth hormone (GH-C53S).

M. Bidlingmaier, C. Flück, P. Mullis, 2005, The Journal of clinical endocrinology and metabolism.

Isolated autosomal dominant growth hormone deficiency: an evolving pituitary deficit? A multicenter follow-up study.

I. Robinson, P. Czernichow, G. Binder, 2005, The Journal of clinical endocrinology and metabolism.

Primary GH insensitivity '(Laron syndrome) caused by a novel 4 kb deletion encompassing exon 5 of the GH receptor gene: effect of intermittent long-term treatment with recombinant human IGF-I.

S. Gallati, P. Mullis, A. Jorge, 2004, European journal of endocrinology.

Reduced longevity in untreated patients with isolated growth hormone deficiency.

S. Gallati, P. Mullis, S. Salemi, 2003, The Journal of clinical endocrinology and metabolism.

New N-terminal located mutation (Q4ter) within the POU1F1-gene (PIT-1) causes recessive combined pituitary hormone deficiency and variable phenotype.

S. Gallati, P. Mullis, R. Pfäffle, 2003, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Instant coffee with high chlorogenic acid levels protects humans against oxidative damage of macromolecules.

Oliver Neubauer, K. Wagner, T. Simić, 2010, Molecular nutrition & food research.

Evaluation of the biological activity of a growth hormone (GH) mutant (R77C) and its impact on GH responsiveness and stature.

M. Thevis, C. Flück, P. Mullis, 2007, The Journal of clinical endocrinology and metabolism.

Regulation of growth-hormone-receptor gene expression by growth hormone and pegvisomant in human mesangial cells.

C. Strasburger, U. Meinhardt, P. Mullis, 2003, Kidney international.