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American Journal of Clinical and Experimental Immunology|January 8, 2024
Hemophagocytic lymphohistiocytosis in children with Griscelli syndrome type 2: genetics, laboratory findings and treatmentEzgi Cay, Ahmet Sezer, Veysel Karakulak, et al.
Nutrients|June 10, 2023
Functional Foods: A Promising Strategy for Restoring Gut Microbiota Diversity Impacted by SARS-CoV-2 VariantsAntara Banerjee, Indumathi Somasundaram, Diptimayee Das, et al.
Future Oncology (London, England)|November 28, 2023
Genetic testing and counseling challenges in personalized breast cancer care: review article with insights from TürkiyeIrfan Cicin, Nuri Karadurmus, Ahmet Bilici, et al.
Journal of Nephrology|June 7, 2021
More than tubular dysfunction: cystinosis and kidney outcomesBahriye Atmis, Aysun K Bayazit, Derya Cevizli, et al.
Research and Practice in Thrombosis and Haemostasis|June 9, 2025
Clinical and laboratory aspects of patients diagnosed with various inherited platelet disordersVeysel Gök, Alper Ozcan, Fatma Türkan Mutlu, et al.
The Journal of Clinical Investigation|January 12, 2016
Molecular etiology of arthrogryposis in multiple families of mostly Turkish originYavuz Bayram, Ender Karaca, Zeynep Coban Akdemir, et al.
The Journal of Clinical Investigation|January 10, 2015
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypesBo Yuan, Davut Pehlivan, Ender Karaca, et al.
Functional & Integrative Genomics|January 31, 2022
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics ConsortiumMunis Dundar, Umut Fahrioglu, Saliha Handan Yildiz, et al.
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