^World Health Organization. World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. 2019. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
^Nitsche MA, Jaussi W, Liebetanz D, Lang N, Tergau F, Paulus W. Consolidation of human motor cortical neuroplasticity by D-cycloserine. Neuropsychopharmacology. August 2004, 29 (8): 1573–8. PMID 15199378. doi:10.1038/sj.npp.1300517.
^Ori R, Amos T, Bergman H, Soares-Weiser K, Ipser JC, Stein DJ. Augmentation of cognitive and behavioural therapies (CBT) with d-cycloserine for anxiety and related disorders. The Cochrane Database of Systematic Reviews. May 2015, 5 (5): CD007803. PMID 25957940. doi:10.1002/14651858.CD007803.pub2.
^ 11.011.111.211.311.4Prosser GA, de Carvalho LP. Kinetic mechanism and inhibition of Mycobacterium tuberculosis D-alanine:D-alanine ligase by the antibiotic D-cycloserine. The FEBS Journal. February 2013, 280 (4): 1150–66. PMID 23286234. S2CID 22305408. doi:10.1111/febs.12108.
^ 12.012.1Kaushal G, Ramirez R, Alambo D, Taupradist W, Choksi K, Sirbu C. Initial characterization of D-cycloserine for future formulation development for anxiety disorders. Drug Discoveries & Therapeutics. October 2011, 5 (5): 253–60. PMID 22466372. doi:10.5582/ddt.2011.v5.5.253.
^Silverman R. An Aromatization Mechanism of Inactivation of γ-Aminobutyric Acid Aminotransferase for the Antibiotic l-Cycloserine. Journal of the American Chemical Society. 1998, 120 (10): 2256–2267. doi:10.1021/ja972907b.
^Kuehl Jr FA, Wolf FJ, Trenner NR, Peck RL, Buhs RP, Howe E, et al. D-4-Amino-3-isoxazolidinone, a new antibiotic. Journal of the American Chemical Society. 1955, 77 (8): 2344–5. doi:10.1021/ja01613a105.
^Hidy PH, Hodge EB, Young VV, Harned RL, Brewer GA, Phillips WF, et al. Synthesis of D-4-amino-3-isoxazolidinone. Journal of the American Chemical Society. 1955, 77 (8): 2346–7. doi:10.1021/ja01613a107.
^Hidy PH, Hodge EB, Young VV, Harned RL, Brewer GA, Phillips WF, et al. Structure and reactions of cycloserine. Journal of the American Chemical Society. 1955, 77 (8): 2345–6. doi:10.1021/ja01613a106.