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Helvetica Paediatrica Acta|April 1, 1978
Intelligence of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency, their parents and unaffected siblingsU Wenzel, M Schneider, M Zachmann, et al.
Biomedical & Environmental Mass Spectrometry|November 1, 1987
Identification of new steroids in patients with 17 alpha-hydroxylase deficiency by capillary gas chromatography/mass spectrometryN Blau, M Zachmann, B Kempken, et al.
Clinical Endocrinology|November 1, 1984
Ovarian steroidogenesis in an adrenalectomized girl with 21-hydroxylase deficiencyM Zachmann, B Manella, B Kempken, et al.
Acta Endocrinologica|February 1, 1982
Transient impairment or delay of urinary trihydroxypregnanone (THS) response to metyrapone in boys with delayed adolescence and in patients with isolated growth hormone deficiencyM Zachmann, D Tassinari, W Sorgo, et al.
Acta Endocrinologica|January 1, 1987
Comparison of two tests to recognize or exclude 5 alpha-reductase deficiency in prepubertal childrenS Greene, M Zachmann, B Manella, et al.
Gynecologic Investigation|January 1, 1976
Male pseudohermaphroditism consistent with 17,20-desmolase deficiencyU Goebelsmann, M Zachmann, V Davajan, et al.
European Journal of Pediatrics|June 1, 1995
Treatment of patients with Ullrich-Turner syndrome with conventional doses of growth hormone and the combination with testosterone or oxandrolone: effect on growth, IGF-I and IGFBP-3 concentrationsG Haeusler, H Frisch, K Schmitt, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1995
Replacement of growth hormone (GH) in normally growing GH-deficient patients operated for craniopharyngiomaE J Schoenle, J Zapf, A Prader, et al.
European Child & Adolescent Psychiatry|January 27, 1998
Psychiatric, neuropediatric, and neuropsychological symptoms in a case of hypomelanosis of ItoM von Aster, M Zachmann, D Brandeis, et al.
Biochimica Et Biophysica Acta|August 25, 1992
Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496)----Cys, Gln(461)----Stop) actually cause combined 17 alpha-hydroxylase/17,20-lyase deficiencyT Yanase, M R Waterman, M Zachmann, et al.
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