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European Journal of Nutrition|February 9, 2016
A khorasan wheat-based replacement diet improves risk profile of patients with type 2 diabetes mellitus (T2DM): a randomized crossover trialAnne Whittaker, Monica Dinu, Francesca Cesari, et al.Case Reports in Endocrinology|May 4, 2017
A Rare Complication following Thyroid Percutaneous Ethanol Injection: Plummer AdenomaRoberto Cesareo, Anda Mihaela Naciu, Valerio Pasqualini, et al.Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 6, 2007
Adherence to a healthful life attenuates lipid parameters among a healthy Italian populationFrancesco Sofi, Anna Maria Gori, Rossella Marcucci, et al.Journal of Thrombosis and Haemostasis : JTH|January 24, 2024
Management of pregnancy and delivery in congenital fibrinogen disorders: communication from the ISTH SSC Subcommittee on Factor XIII and FibrinogenAlessandro Casini, Rezan Abdul Kadir, Magy Abdelwahab, et al.Clinical Chemistry|May 21, 2005
Endothelial nitric oxide synthase -786T>C, but not 894G>T and 4a4b, polymorphism influences plasma homocysteine concentrations in persons with normal vitamin statusCinzia Fatini, Francesco Sofi, Anna Maria Gori, et al.Thrombosis and Haemostasis|October 18, 2018
Mutational Epidemiology of Congenital Fibrinogen DisordersAlessandro Casini, Marc Blondon, Veronique Tintillier, et al.Gastroenterology|June 11, 2002
Antidiabetic thiazolidinediones inhibit collagen synthesis and hepatic stellate cell activation in vivo and in vitroAndrea Galli, David W Crabb, Elisabetta Ceni, et al.Atherosclerosis|July 3, 2007
Fish intake and LPA 93C>T polymorphism: gene-environment interaction in modulating lipoprotein (a) concentrationsFrancesco Sofi, Cinzia Fatini, Elena Sticchi, et al.Journal of the American College of Nutrition|April 14, 2018
A Khorasan Wheat-Based Replacement Diet Improves Risk Profile of Patients With Nonalcoholic Fatty Liver Disease (NAFLD): A Randomized Clinical TrialMonica Dinu, Anne Whittaker, Giuditta Pagliai, et al.Haematologica|July 1, 2021
A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish familyMichel Guipponi, Frédéric Masclaux, Frédérique Sloan-Béna, et al.Pageof 15