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Page 1
Short stature caused by a biologically inactive mutant growth hormone (GH-C53S).
Besson A, Salemi S, Deladoëy J, Vuissoz JM, Eblé A, Bidlingmaier M, Bürgi S, Honegger U, Flück C, Mullis PE. Besson A, et al. Among authors: bidlingmaier m. J Clin Endocrinol Metab. 2005 May;90(5):2493-9. doi: 10.1210/jc.2004-1838. Epub 2005 Feb 15. J Clin Endocrinol Metab. 2005. PMID: 15713716
Ghrelin drives GH secretion during fasting in man.
Muller AF, Lamberts SW, Janssen JA, Hofland LJ, Koetsveld PV, Bidlingmaier M, Strasburger CJ, Ghigo E, Van der Lely AJ. Muller AF, et al. Among authors: bidlingmaier m. Eur J Endocrinol. 2002 Feb;146(2):203-7. doi: 10.1530/eje.0.1460203. Eur J Endocrinol. 2002. PMID: 11834429 Free article. Clinical Trial.
Efficacy of 12-month treatment with the GH receptor antagonist pegvisomant in patients with acromegaly resistant to long-term, high-dose somatostatin analog treatment: effect on IGF-I levels, tumor mass, hypertension and glucose tolerance.
Colao A, Pivonello R, Auriemma RS, De Martino MC, Bidlingmaier M, Briganti F, Tortora F, Burman P, Kourides IA, Strasburger CJ, Lombardi G. Colao A, et al. Among authors: bidlingmaier m. Eur J Endocrinol. 2006 Mar;154(3):467-77. doi: 10.1530/eje.1.02112. Eur J Endocrinol. 2006. PMID: 16498061
365 results