Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Archives of Rheumatology|September 16, 2021
Investigation of Genes Associated With Atherosclerosis in Patients With Systemic Lupus ErythematosusMehmet Ali Balci, Engin Atli, Hakan GüRKAN
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 11, 2013
A novel biometric authentication approach using electrocardiogram signalsHakan Gürkan, Umit Guz, B S Yarman
Balkan Medical Journal|September 11, 2014
Results of Mitochondrial DNA Sequence Analysis in Patients with Clinically Diagnosed Leber's Hereditary Optic NeuropathyHakan Gürkan, Sadık Altan Ozal, Haluk Esgin
Journal of Electrocardiology|October 15, 2025
A novel multichannel sparse convolutional autoencoder for electrocardiogram signal compressionTahir Bekiryazıcı, Mehmet Damkacı, Gürkan Aydemir, et al.
The Turkish Journal of Pediatrics|January 29, 2020
A novel LEMD3 pathogenic variant in a son and mother with osteopoikilosisSelin Elmaoğulları, Adelet Elçin Yıldız, Selma Demir, et al.
Noro Psikiyatri Arsivi|September 11, 2024
Investigation of Pogz Gene Variants in Non-Syndromic Autism Spectrum DisorderJülide Tozkır, Gökberk Yıldırım, Selma Demir, et al.
Balkan Medical Journal|April 27, 2017
Lack of Association Between Toll-like Receptor 2 Polymorphisms (R753Q and A-16934T) and Atopic Dermatitis in Children from Thrace Region of TurkeyCeren Can, Mehtap Yazıcıoğlu, Hakan Gürkan, et al.
Molecular Syndromology|March 29, 2021
Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case ReportSelma Demir, Hakan Gürkan, Veysel Öz, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 13, 2022
A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deletion SyndromeHümeyra Yaşar Köstek, Fatma Özgüç Çömlek, Hakan Gürkan, et al.
Balkan Medical Journal|November 14, 2022
Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing TechniqueEngin Atlı, Hakan Gürkan, Babürhan Güldiken, et al.
Pageof 3