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Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|February 9, 2018
Insulin-Leptin Axis, Cardiometabolic Risk and Oxidative Stress in Elderly with Metabolic SyndromeDaniela Gradinaru, Husseina Khaddour, Denisa Margina, et al.Health Policy (Amsterdam, Netherlands)|March 12, 2023
Evaluation of a national e-booking system for medical consultation in primary care in a universal health systemAude Motulsky, Delphine Bosson-Rieutort, Susan Usher, et al.Mechanisms of Ageing and Development|March 18, 2014
Diet fatty acid profile, membrane composition and lifespan: an experimental study using the blowfly (Calliphora stygia)Megan A Kelly, Michael J Usher, Beata Ujvari, et al.Journal of Structural Biology|June 11, 2021
Crystal structure of the anti-CRISPR repressor Aca2Ben Usher, Nils Birkholz, Izaak N Beck, et al.JIMD Reports|February 20, 2020
An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming beltHava Peretz, Michael Korostishevsky, David M Steinberg, et al.Diabetic Medicine : a Journal of the British Diabetic Association|March 8, 2020
Barriers to completing oral glucose tolerance testing in women at risk of gestational diabetesE H Lachmann, R A Fox, R A Dennison, et al.BJU International|September 19, 2021
Validation and public health modelling of risk prediction models for kidney cancer using the UK BiobankHannah Harrison, Lisa Pennells, Angela Wood, et al.Thrombosis Research|May 12, 2009
Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosisEinor Ben Assayag, Shani Shenhar-Tsarfaty, Irena Bova, et al.JIMD Reports|February 23, 2013
Identification of 11 Novel Homogentisate 1,2 Dioxygenase Variants in Alkaptonuria Patients and Establishment of a Novel LOVD-Based HGD Mutation DatabaseAndrea Zatkova, Tatiana Sedlackova, Jan Radvansky, et al.Clinical Chemistry and Laboratory Medicine|November 7, 1998
Screening for tumour suppressor p16(CDKN2A) germline mutations in Israeli melanoma familiesE A Yakobson, A Zlotogorski, R Shafir, et al.Pageof 140