Ten Novel Mutations in the NR5A1 Gene Cause Disordered Sex Development in 46,XY and Ovarian Insufficiency in 46,XX Individuals von Camats, N, Pandey, A. V, Fernández-Cancio, M, Andaluz, P, Janner, M, Torán, N, Moreno, F, Bereket, A, Akcay, T, García-García, E, Muñoz, M. T, Gracia, R, Nistal, M, Castaño, L, Mullis, P. E, Carrascosa, A, Audí, L, Flück, C. E

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Positional cloning of the APECED gene von Nagamine, Kentaro, Peterson, Pärt, Scott, Hamish S, Kudoh, Jun, Minoshima, Shinsei, Heino, Maarit, Krohn, Kai J. E, Lalioti, Maria D, Mullis, Primus E, Antonarakis, Stylianos E, Kawasaki, Kazuhiko, Asakawa, Shuichi, Ito, Fumiaki, Shimizu, Nobuyoshi

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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... von MULLIS, P. E, YOSHIMURA, N, KUHLMANN, B, LIPPUNER, K, JAEGER, P, HARADA, H

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Mutations in PROP1 cause familial combined pituitary hormone deficiency von Wu, Wei, Cogan, Joy D., Pfäffle, Roland W., Dasen, Jeremy S., Frisch, Herwig, O'Connell, Shawn M., Flynn, Sarah E., Brown, Milton R., Mullis, Primus E., Parks, John S., Phillips III, John A., Rosenfeld, Michael G.

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Do centimetres matter? Self-reported versus estimated height measurements in parents von Gozzi, T, Flück, CE, L'Allemand, D, Dattani, MT, Hindmarsh, PC, Mullis, PE

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Epidemiology of Type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade von SCHOENLE, E. J, LANG-MURITANO, M, GSCHWEND, S, LAIMBACHER, J, MULLIS, P. E, TORRESANI, T, BIASON-LAUBER, A, MOLINARI, L

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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 von Tonella, P., Flück, C.E., Mullis, P.-E.

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Prospective randomised treatment with recombinant human growth hormone in cystic fibrosis von Schibler, A, von der Heiden, R, Birrer, P, Mullis, P E

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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) von FLÜCK, C, DELADOEY, J, RUTISHAUSER, K, EBLE, A, MARTI, U, WEI WU, MULLIS, P. E

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Hot spot in the PROP1 gene responsible for combined pituitary hormone deficiency von DELADOËY, J, FLÜCK, C, BÜYÜKGEBIZ, A, KUHLMANN, B. V, EBLE, A, HINDMARSH, P. C, WEI WU, MULLIS, P. E

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Isolated GH deficiency (IGHD) type II: imaging of the pituitary gland by magnetic resonance reveals characteristic differences in comparison with severe IGHD of unknown origin von BINDER, G, NAGEL, B. H. P, RANKE, M. B, MULLIS, P. E

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Microalbuminuria in diabetes mellitus: Efficacy of a new screening method in comparison with timed overnight urine collection von Meinhardt, U., Ammann, R.A., Flück, C., Diem, P., Mullis, P.E.

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Genetic homogeneity of autoimmune polyglandular disease type I von BJÖRSES, P, AALTONEN, J, MULLIS, P. E, POHL, M, RITZEN, M, ROMEO, G, SHAPIRO, M. S, SMITH, C. S, SOLYOM, J, ZLOTOGORA, J, PELTONEN, L, VIKMAN, A, PERHEENTUPA, J, BEN-ZION, G, CHIUMELLO, G, DAHL, N, HEIDEMAN, P, HOORWEG-NIJMAN, J. J. G, MATHIVON, L

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High prevalence of vitamin D deficiency in children and adolescents with type 1 diabetes von Janner, Marco, Ballinari, Pietro, Mullis, Primus E, Flück, Christa E

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Prevalence of human GH-1 gene alterations in patients with isolated growth hormone deficiency von WAGNER, J. K, EBLE, A, HINDMARSH, P. C, MULLIS, P. E

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Pituitary Gland Development: An Update von Bancalari, Rodrigo E., Gregory, Louise C., McCabe, Mark J., Dattani, Mehul T.

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Isolated Growth Hormone Deficiency Type 2: From Gene to Therapy von Miletta, Maria Consolata, Lochmatter, Didier, Petkovic, Vibor, Mullis, Primus-E.

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Downstream Insulin-Like Growth Factor von Pfäffle, Roland, Kiess, Wieland, Klammt, Jürgen

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Pituitary Gland Imaging and Outcome von Di Iorgi, Natascia, Morana, Giovanni, Gallizia, Anna Lisa, Maghnie, Mohamad

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Spectrum of Insulin-Like Growth Factor Deficiency von Wit, Jan M., Oostdijk, W., Losekoot, M.

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