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Hauri-Hohl, A; Meyer-Böni, M; Lang-Muritano, M; Hauri-Hohl, M; Schoenle, E J; Biason-Lauber, A (2011). Aromatase deficiency due to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene. Clinical Endocrinology, 75(1):39-43.
Rosa, S; Steigert, M; Lang-Muritano, M; l'Allemand, D; Schoenle, E J; Biason-Lauber, A (2010). Clinical, genetic and functional characteristics of three novel CYP17A1 mutations causing combined 17alpha-hydroxylase/17,20-lyase deficiency. Hormone Research in Paediatrics, 73(3):198-204.
Sahakitrungruang, T; Soccio, R E; Lang-Muritano, M; Walker, J M; Achermann, J C; Miller, W L (2010). Clinical, genetic, and functional characterization of four patients carrying partial loss-of-function mutations in the steroidogenic acute regulatory protein (StAR). Journal of Clinical Endocrinology and Metabolism, 95(7):3352-2259.
Chan, Y M; de Guillebon, A; Lang-Muritano, M; Plummer, L; Cerrato, F; Tsiaras, S; Gaspert, A; Lavoie, H B; Wu, C H; Crowley, W F; Amory, J K; Pitteloud, N; Seminara, S B (2009). GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 106(28):11703-11708.
Dimitropoulos, A; Molinari, L; Etter, K; Torresani, T; Lang-Muritano, M; Jenni, O G; Largo, R H; Latal, B (2009). Children with congenital hypothyroidism: long-term intellectual outcome after early high-dose treatment. Pediatric Research, 65(2):242-248.
Braun, D; Konrad, D; Lang-Muritano, M; Schoenle, E (2008). Improved glycemic control and lower frequency of severe hypoglycemia with insulin detemir; long-term experience in 105 children and adolescents with type 1 diabetes. Pediatric Diabetes, 9(4 Part):382-387.