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Journal of Pediatric Endocrinology & Metabolism : JPEM|November 26, 1998
Female pseudohermaphroditism associated with a novel homozygous G-to-A (V370-to-M) substitution in the P-450 aromatase geneM Ludwig, A Beck, L Wickert, et al.
Human Genetics|September 10, 1999
X-linked adrenomyeloneuropathy associated with 14 novel ALD-gene mutations: no correlation between type of mutation and age of onsetM Wichers, W Köhler, W Brennemann, et al.
Neuroscience Letters|August 11, 2000
Expression of mineralocorticoid and glucocorticoid receptor mRNA in the human hippocampusM Watzka, S Beyenburg, I Blümcke, et al.
American Journal of Obstetrics and Gynecology|October 15, 1979
Simultaneous determination of seven unconjugated steroids in maternal venous and umbilical arterial and venous serum in elective and emergency cesarean section at termW G Sippell, H G Dörr, H Becker, et al.
Aviation, Space, and Environmental Medicine|October 1, 1985
Serum levels of eleven steroid hormones following motion sicknessG K Stalla, H G Doerr, F Bidlingmaier, et al.
Biochemical and Biophysical Research Communications|April 16, 1998
Expression of CYP19 (aromatase) mRNA in the human temporal lobeB Stoffel-Wagner, M Watzka, S Steckelbroeck, et al.
Journal of Neuroendocrinology|September 6, 2000
Differential mRNA expression of the two mineralocorticoid receptor splice variants within the human brain: structure analysis of their different DNA binding domainsL Wickert, J Selbig, M Watzka, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1984
Virilization without adrenal hyperplasia in 21-hydroxylase deficiency during fetal lifeU Kuhnle, N Böhm, G Wolff, et al.
Journal of Neuroendocrinology|May 21, 1999
Characterization of 17beta-hydroxysteroid dehydrogenase activity in brain tissue: testosterone formation in the human temporal lobeS Steckelbroeck, B Stoffel-Wagner, R Reichelt, et al.
American Journal of Human Genetics|December 1, 1994
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M alleleJ P Faber, W Poller, S Weidinger, et al.
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