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The Journal of Steroid Biochemistry and Molecular Biology|June 1, 1995
Defects in steroidogenic enzymes. Discrepancies between clinical steroid research and molecular biology resultsM ZachmannFortschritte Der Medizin|April 10, 1993
[Hypogonadism and delayed puberty. Indications for androgen treatment in adolescents]M ZachmannPostgraduate Medical Journal|January 1, 1978
Diagnosis of treatable types of short and tall statureM ZachmannHormone Research|January 1, 1992
Familial adrenal feminization probably due to increased steroid aromatizationE Leiberman, M ZachmannActa Endocrinologica|November 1, 1979
Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency confirmed by HLA tissue typingM Zachmann, A PraderHelvetica Paediatrica Acta|September 1, 1982
[Virilization caused by methandrostenolone-containing cream in 2 prepubertal girls]W Sorgo, M ZachmannActa Endocrinologica|March 1, 1978
Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyM Zachmann, A PraderEnzyme|January 1, 1977
Leucocyte energy metabolism. VI. Simultaneous and improved isolation of lymphocytes and polymorphonuclear leucocytes from a single of human bloodP Nessi, J FreiNeurosurgery|March 1, 1991
Results of transsphenoidal extirpation of craniopharyngiomas and Rathke's cystsA M Landolt, M ZachmannThe Journal of Clinical Endocrinology and Metabolism|February 1, 1983
Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patientsM Zachmann, D Tassinari, A PraderPageof 11