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Clinical Toxicology (Philadelphia, Pa.)|September 3, 2019
Prevalence of fentanyl exposure and knowledge regarding the risk of its use among emergency department patients with active opioid use history at an urban medical center in Baltimore, MarylandH Bach, V Jenkins, A Aledhaim, et al.
European Journal of Cancer (Oxford, England : 1990)|January 20, 1999
Attitudes of patients to randomised clinical trials of cancer therapyL J Fallowfield, V Jenkins, C Brennan, et al.
British Journal of Cancer|March 21, 2013
Drivers and barriers to patient participation in RCTsV Jenkins, V Farewell, D Farewell, et al.
Breast (Edinburgh, Scotland)|August 30, 2011
A pilot study to examine the experiences and attitudes of women with breast cancer towards one versus two-step axillary surgeryV Jenkins, H Harder, M Babar, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 13, 2010
Thrombin generation in haemophilia A patients with mutations causing factor VIII assay discrepancyR Gilmore, S Harmon, C Gannon, et al.
Clinical Science (London, England : 1979)|May 1, 1995
Glucocorticoid-suppressible hyperaldosteronism: effects of crossover site and parental origin of chimaeric gene on phenotypic expressionA Jamieson, L Slutsker, G C Inglis, et al.
Molecular Biology & Medicine|October 1, 1986
Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene regionB O Boehm, C Rosak, T L Boehm, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1987
Cloning of cDNA encoding steroid 11 beta-hydroxylase (P450c11)S C Chua, P Szabo, A Vitek, et al.
Circulation|March 11, 1998
Associations between human aldosterone synthase (CYP11B2) gene polymorphisms and left ventricular size, mass, and functionM Kupari, A Hautanen, L Lankinen, et al.
Molecular Endocrinology (Baltimore, Md.)|May 1, 1991
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency alleleM T Tusie-Luna, P W Speiser, M Dumic, et al.
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