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Pediatric Nephrology (Berlin, Germany)|November 30, 2000
Renal function in pediatric patients with beta-thalassemia majorB Aldudak, A Karabay Bayazit, A Noyan, et al.The International Journal of Artificial Organs|December 6, 2003
A novel biodegradable PCL film for tendon reconstruction: Achilles tendon defect model in ratsC Kazimoğlu, S Bölükbaşi, U Kanatli, et al.International Journal of Dermatology|March 8, 2021
Evaluation of biophysical skin parameters and hair changes in patients with acne vulgaris treated with isotretinoin, and the effect of biotin use on these parametersSema E Aksac, Serap G Bilgili, Goknur O Yavuz, et al.Journal of Trace Elements and Electrolytes in Health and Disease|March 1, 1988
Zinc status in pregnancy and the occurrence of anencephaly in TurkeyA O Cavdar, M Bahçeci, N Akar, et al.Transplantation Proceedings|November 19, 2017
Comparision of Ureteral Stent Colonization Between Deceased and Live Donor Renal Transplant RecipientsM Sarier, D Seyman, S Tekin, et al.Transplantation Proceedings|July 25, 2017
Results of Real-time Multiplex Polymerase Chain Reaction Assay in Renal Transplant Recipients With Sterile PyuriaM Sarier, M Demir, S Goktas, et al.Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|July 16, 2013
Effects of ivabradine on 6-minute walk test and quality of life in patients with previously implanted CRT-DIsmail Ates, Asuman H Yavuz, Mehmet Doğru, et al.Clinical Genetics|July 31, 2018
A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab childrenH Yavuz, A M Bertoli-Avella, M Alfadhel, et al.Italian Journal of Dermatology and Venereology|November 12, 2020
Correlation study between clinical classification and disability index in a holistic evaluation of acne severity and impact in TurkeyEmin Ozlu, Ayse S Karadag, Berna Aksoy, et al.Archives of Endocrinology and Metabolism|February 8, 2018
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencingFernanda A Correa, Marcela M França, Qing Fang, et al.Pageof 8