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Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|August 15, 2000
Inhibition of gastric mucosal damage by methylglyoxal pretreatment in ratsO A Al-Shabanah, S Qureshi, M M Al-Harbi, et al.Cellular Signalling|February 19, 2017
GPR43 activation enhances psoriasis-like inflammation through epidermal upregulation of IL-6 and dual oxidase 2 signaling in a murine modelAhmed Nadeem, Sheikh F Ahmad, Naif O Al-Harbi, et al.Saudi Medical Journal|February 27, 2015
Angiotensin-converting enzyme gene insertion/deletion polymorphism in Saudi patients with rheumatic heart diseaseKhalid M Al-Harbi, Ibrahim S Almuzaini, Mohamed M Morsy, et al.American Journal of Medical Genetics. Part A|October 12, 2021
Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB geneTalal M Al-Harbi, Haya Al-Rammah, Naif Al-Zahrani, et al.Clinical and Diagnostic Laboratory Immunology|July 10, 2004
HLA class II profile and distribution of HLA-DRB1 and HLA-DQB1 alleles and haplotypes among Lebanese and Bahraini ArabsWassim Y Almawi, Marc Busson, Hala Tamim, et al.Cardiovascular Endocrinology & Metabolism|January 31, 2022
Hormonal and metabolic profiles of obese and nonobese type 2 diabetes patients: implications of plasma insulin, ghrelin, and vitamin D levelsHayder A Giha, Dhuha M B AlDehaini, Faris E Joatar, et al.Hormone Research in Paediatrics|January 31, 2015
Natural history and management of congenital hypothyroidism with in situ thyroid glandMireille Castanet, Alexandra Goischke, Juliane Léger, et al.Toxins|December 22, 2023
Cytotoxicity and Radiosensitizing Potentials of Pilosulin-3, a Recombinant Ant Venom, in Breast Cancer CellsReema M Alzeer, Khaled S Al-Hadyan, Najla M Al-Harbi, et al.Pediatric Cardiology|August 10, 2015
IL10 Promoter Polymorphisms are Associated with Rheumatic Heart Disease in Saudi Arabian PatientsAtiyeh M Abdallah, Aisha Alnuzha, Abdulhadi H Al-Mazroea, et al.European Review for Medical and Pharmacological Sciences|March 7, 2019
Next-generation sequencing identifies a homozygous mutation in ACADVL associated with pediatric familial dilated cardiomyopathyS J Carlus, I S Almuzaini, M Karthikeyan, et al.Pageof 18