Tham khảo Methandriol

  1. 1 2 J. Elks (14 tháng 11 năm 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. tr. 794–. ISBN 978-1-4757-2085-3.
  2. 1 2 I.K. Morton; Judith M. Hall (6 tháng 12 năm 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. tr. 177–. ISBN 978-94-011-4439-1.
  3. 1 2 Henderson, Edward; Weinberg, Marvin (1951). “Methylandrostenediol”. The Journal of Clinical Endocrinology & Metabolism. 11 (6): 641–652. doi:10.1210/jcem-11-6-641. ISSN 0021-972X.
  4. ↑ Homburger, F.; Kasdon, S. C.; Fishman, W. H. (1950). “Methylandrostenediol: A Non-Virilizing Derivative of Testosterone in Metastatic Cancer of the Breast”. Experimental Biology and Medicine. 74 (1): 162–164. doi:10.3181/00379727-74-17840. ISSN 1535-3702.
  5. ↑ Kasdon, S. C. (1952). “Methylandrostenediol in palliative treatment of breast cancer”. JAMA: The Journal of the American Medical Association. 148 (14): 1212. doi:10.1001/jama.1952.02930140044014. ISSN 0098-7484.
  6. ↑ Segaloff, Albert; Gordon, Douglas; Horwitt, Benjamin N.; Schlosser, Joseph V.; Murison, Paul J. (1952). “Hormonal therapy in cancer of the breast.II. Effect of methylandrostenediol on clinical course and hormonal excretion”. Cancer. 5 (2): 271–274. doi:10.1002/1097-0142(195203)5:2<271::AID-CNCR2820050212>3.0.CO;2-W. ISSN 0008-543X.
  7. ↑ Harold Gardiner-Hill (1958). Modern Trends in Endocrinology. Butterworth. tr. 235. Foss (1956), using methylandrostenediol in doses of 100 milligrams daily in the treatment of patients with inoperable carcinoma of the breast, found it almost as virilizing as testosterone propionate or methyltestosterone in comparable doses.
  8. ↑ https://www.drugs.com/international/methandriol.html
  9. ↑ Heinrich Kahr (8 tháng 3 năm 2013). Konservative Therapie der Frauenkrankheiten: Anzeigen, Grenzen und Methoden Einschliesslich der Rezeptur. Springer-Verlag. tr. 21–. ISBN 978-3-7091-5694-0.
  10. ↑ Schänzer W (1996). “Metabolism of anabolic androgenic steroids”. Clin. Chem. 42 (7): 1001–20. PMID 8674183.
  11. ↑ Ruzicka, L.; Goldberg, M. W.; Rosenberg, H. R. (1935). “Sexualhormone X. Herstellung des 17-Methyl-testosterons und anderer Androsten- und Androstanderivate. Zusammenhänge zwischen chemischer Konstitution und männlicher Hormonwirkung”. Helvetica Chimica Acta. 18 (1): 1487–1498. doi:10.1002/hlca.193501801203. ISSN 0018-019X.