Mullis, P E

Tonella, P; Flück, C E; Mullis, P E (2010). Metabolic control of type 1 diabetic patients followed at the University Children's Hospital in Berne: Have we reached the goal? Swiss medical weekly, 140, w13057. Muttenz: EMH Schweizerischer Ärzteverlag 10.4414/smw.2010.13057

Tonella, P; Flück, C E; Mullis, P E (2010). Insulin-like growth factor-I treatment in primary growth hormone insensitivity: effect of recombinant human IGF-I (rhIGF-I) and rhIGF-I/rhIGF-binding protein-3 complex. Hormone research in paediatrics, 73(2), pp. 140-7. Basel: Karger 10.1159/000277660

Gozzi, T; Flück, Ce; L'allemand, D; Dattani, M T; Hindmarsh, P C; Mullis, P E (2010). Do centimetres matter? Self-reported versus estimated height measurements in parents. Acta paediatrica, 99(4), pp. 569-74. Oslo: Wiley 10.1111/j.1651-2227.2009.01654.x

Scheidegger, U A; Flück, C E; Scheidegger, K; Diem, P; Mullis, P E (2009). [Role of complementary medicine in type 1 diabetes mellitus in two Swiss centres]. Praxis - schweizerische Rundschau für Medizin, 98(18), pp. 1001-5. Bern: Huber

Oestmann, A; Mullis, P E; Stanga, Z (2009). [Hermaphroditos in Greek mythology--DSD in moderne medicine]. Praxis - schweizerische Rundschau für Medizin, 98(1), pp. 31-4. Bern: Huber

Binder, G; Iliev, D I; Mullis, P E; Ranke, M B (2007). Catch-up growth in autosomal dominant isolated growth hormone deficiency (IGHD type II). Growth hormone & IGF research, 17(3), pp. 242-8. Oxford: Elsevier 10.1016/j.ghir.2007.01.014

Spörri, D; Mullis, P E (2006). [Sun-tanned and still not healthy!]. Praxis - schweizerische Rundschau für Medizin, 95(29-30), pp. 1135-9. Bern: Huber

von der Heiden, R; Balestra, A P G; Bianchetti, M G; Casaulta Aebischer, C; Mullis, P E; Lippuner, K; Jaeger, P (2003). Which factors account for renal stone formation in cystic fibrosis? Clinical nephrology, 59(3), pp. 160-3. München-Deisenhofen: Dustri-Verlag

Ramelli, G P; von der Weid, N; Stanga, Z; Mullis, P E; Buergi, U (1998). Suprasellar germinomas in childhood and adolescence: diagnostic pitfalls. Journal of pediatric endocrinology & metabolism, 11(6), pp. 693-7. Berlin: De Gruyter 10.1515/JPEM.1998.11.6.693

Mullis, P E; Yoshimura, N; Kuhlmann, B; Lippuner, K; Jaeger, P; Harada, H (1997). Aromatase deficiency in a female who is compound heterozygote for two new point mutations in the P450arom gene: impact of estrogens on hypergonadotropic hypogonadism, multicystic ovaries, and bone densitometry in childhood. Journal of clinical endocrinology and metabolism, 82(6), pp. 1739-45. Chevy Chase, Md.: Endocrine Society 10.1210/jc.82.6.1739