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Janner, M.; Mullis, P. E. (2007). Impaired calcium homeostasis, clinical impact. Therapeutische Umschau, 64(5), pp. 271-275. Bern: Huber
Janner, M.; Mullis, P. E.; Flück, C. E. (2006). Is the metabolic syndrome a new childhood disease? Praxis - schweizerische Rundschau für Medizin, 95(13), pp. 493-500. Bern: Huber
Nuoffer, Jean-Marc; Mullis, P. E. (2005). Hypoglykämien – Diagnostik und Therapie im Notfall. Therapeutische Umschau, 62(8), pp. 543-548. Huber 10.1024/0040-5930.62.8.543
Janner, M.; Mullis, P. E. (2005). Osteonpenia and pathological fractures in an adolescent with lactose intolerance and high oxalate intake. Monatsschrift Kinderheilkunde, 153(4), pp. 360-363. Springer-Verlag 10.1007/s00112-003-0773-3
Flück, Christa; Deladoey, J.; Rutishauser, K.; Eblé, A.; Marti, U.; Wu, W.; Mullis, P. E. (1998). Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C). Journal of clinical endocrinology and metabolism, 83(10), pp. 3727-3734. Endocrine Society 10.1210/jcem.83.10.5172
Nuoffer, Jean-Marc; Mullis, P. E.; Wiesmann, U. N. (1997). Treatment with low-dose diazoxide in two growth-retarded prepubertal girls with glycogen storage disease type Ia resulted in catch-up growth. Journal of inherited metabolic disease, 20(6), pp. 790-798. Kluwer Academic Publishers 10.1023/a:1005319818015
Janner, M.; Knill, S. E.; Diem, P.; Zuppinger, K. A.; Mullis, P. E. (1994). Persistent microalbuminuria in adolescents with type I (insulin-dependent) diabetes mellitus is associated to early rather than late puberty. Results of a prospective longitudinal study. European journal of pediatrics, 153(6), pp. 403-408. Berlin: Springer 10.1007/s004310050162
