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Anadolu Kardiyoloji Dergisi : AKD = the Anatolian Journal of Cardiology|July 10, 2002
[The evaluation of the severity of mitral regurgitation using color Doppler echocardiographic methods]M Eren, B Dağdeviren, O Bolca, et al.Journal of Thrombosis and Haemostasis : JTH|November 25, 2003
Tissue- and agonist-specific regulation of human and murine plasminogen activator inhibitor-1 promoters in transgenic miceM Eren, C A Painter, L A Gleaves, et al.American Journal of Industrial Medicine|January 1, 1990
Multiplane gallium tomography in assessment of occupational chest diseasesE M Cordasco, J O'Donnell, W MacIntyre, et al.Seminars in Arthritis and Rheumatism|February 22, 2001
Polyarteritis nodosa in patients with Familial Mediterranean Fever (FMF): a concomitant disease or a feature of FMF?S Ozen, E Ben-Chetrit, A Bakkaloglu, et al.Ophthalmology Science|June 17, 2024
Visual Function Measurements in Eyes With Diabetic Retinopathy: An Expert Opinion on Available MeasuresAdam R Glassman, Mohamed Ashraf Elmasry, Darrell E Baskin, et al.Circulation. Cardiovascular Genetics|August 24, 2010
Novel nonmajor histocompatibility complex-linked loci from mouse chromosome 17 confer susceptibility to viral-mediated chronic autoimmune myocarditisMaya C Poffenberger, Iryna Shanina, Connie Aw, et al.Journal of Medical Genetics|February 5, 2003
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosisK J Borthwick, N Kandemir, R Topaloglu, et al.Annals of the Rheumatic Diseases|December 3, 2005
EULAR/PReS endorsed consensus criteria for the classification of childhood vasculitidesS Ozen, N Ruperto, M J Dillon, et al.American Journal of Human Genetics|December 1, 1999
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34F E Karet, K E Finberg, A Nayir, et al.Human Mutation|September 12, 2000
MEFV mutations in Behçet's diseaseI Touitou, X Magne, N Molinari, et al.Pageof 28