Facial reconstruction

Search LJMU Research Online

Browse Repository | Browse E-Theses

Items where Author is "Adejare, A"

Up a level
Export as [feed] Atom [feed] RSS
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 6.

Article

Frankenfeld, F, Wagmann, L, Abelian, A, Wallach, J, Adejare, A, Brandt, SD and Meyer, MR (2024) In vivo and in vitro metabolic fate and urinary detectability of five deschloroketamine derivatives studied by means of hyphenated mass spectrometry. Metabolites, 14 (5). ISSN 2218-1989

Dybek, M, Wallach, J, Kavanagh, PV, Colestock, T, Filbman, N, Dowling, G, Westphal, F, Elliott, SP, Adejare, A and Brandt, SD (2019) Syntheses and analytical characterizations of the research chemical 1-[1-(2-fluorophenyl)-2-phenylethyl]pyrrolidine (fluorolintane) and five of its isomers. Drug Testing and Analysis, 11 (8). pp. 1144-1161. ISSN 1942-7611

Wallach, J, Colestock, T, Agramunt, J, Claydon, MDB, Dybek, M, Filemban, N, Chatha, M, Halberstadt, AL, Brandt, SD, Lodge, D, Bortolotto, ZA and Adejare, A (2019) Pharmacological characterizations of the 'legal high' fluorolintane and isomers. Behavioural Processes. ISSN 0376-6357

Colestock, C, Wallach, J, Mansi, M, Filemban, N, Morris, H, Elliott, SP, Westphal, F, Brandt, SD and Adejare, A (2017) Syntheses, analytical and pharmacological characterizations of the “legal high” 4-[1-(3-methoxyphenyl)cyclohexyl]morpholine (3-MeO-PCMo) and analogues. Drug Testing and Analysis. ISSN 1942-7611

Wallach, J, Kang, H, Colestock, T, Morris, H, Bortolotto, ZA, Collingridge, GL, Lodge, D, Halberstadt, AL, Brandt, SD and Adejare, A (2016) Pharmacological Investigations of the Dissociative ‘Legal Highs’ Diphenidine, Methoxphenidine and Analogues. PLoS One, 11 (6). ISSN 1932-6203

Wallach, J, Colestock, T, Cicali, B, Elliott, SP, Kavanagh, PV, Adejare, A, Dempster, NM and Brandt, SD (2015) Syntheses and analytical characterizations of N-alkyl-arylcyclohexylamines. Drug Testing and Analysis. ISSN 1942-7611

This list was generated on Wed Jul 17 18:10:13 2024 UTC.