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Results:
1-7
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Results: 7
Authors:
Lang-Muritano, M
Biason-Lauber, A
Gitzelmann, C
Belville, C
Picard, Y
Schoenle, EJ
Citation: M. Lang-muritano et al., A novel mutation in the anti-mullerian hormone gene as cause of persistentmullerian duct syndrome, EUR J PED, 160(11), 2001, pp. 652-654
Authors:
Schoenle, EJ
Lang-Muritano, M
Gschwend, S
Laimbacher, J
Mullis, PE
Torresani, T
Biason-Lauber, A
Molinari, L
Citation: Ej. Schoenle et al., Epidemiology of Type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade, DIABETOLOG, 44(3), 2001, pp. 286-289
Authors:
Biason-Lauber, A
Suter, SL
Shackleton, CHL
Zachmann, M
Citation: A. Biason-lauber et al., Apparent cortisone reductase deficiency: A rare cause of hyperandrogenemiaand hypercortisolism, HORMONE RES, 53(5), 2000, pp. 260-266
Authors:
I'Allemand, D
Biason-Lauber, A
Citation: D. I'Allemand et A. Biason-lauber, Intra-adrenal regulation of androgen synthesis, EUR J CL IN, 30, 2000, pp. 28-33
Authors:
Biason-Lauber, A
Zachmann, M
Schoenle, EJ
Citation: A. Biason-lauber et al., Effect of leptin on CYP17 enzymatic activates in human adrenal cells: New insight in the onset of adrenarche, ENDOCRINOL, 141(4), 2000, pp. 1446-1454
Authors:
Schmitt, S
Biason-Lauber, A
Betts, D
Schoenle, EJ
Citation: S. Schmitt et al., Genomic structure, chromosomal localization, and expression pattern of thehuman LIM-Homeobox3 (LHX 3) gene, BIOC BIOP R, 274(1), 2000, pp. 49-56
Authors:
Biason-Lauber, A
Schoenle, EJ
Citation: A. Biason-lauber et Ej. Schoenle, Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency, AM J HU GEN, 67(6), 2000, pp. 1563-1568
Risultati:
1-7
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