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Journal of Clinical Medicine|December 24, 2021
Circulating IgG Levels in SARS-CoV-2 Convalescent Individuals in CyprusIoannis Mamais, Apostolos Malatras, Gregory Papagregoriou, et al.Investigative Genetics|February 13, 2016
Y-chromosome phylogeographic analysis of the Greek-Cypriot population reveals elements consistent with Neolithic and Bronze Age settlementsKonstantinos Voskarides, Stéphane Mazières, Despina Hadjipanagi, et al.Frontiers in Genetics|July 1, 2024
Risk mapping for better governance in biobanking: the case of biobank.cyKaya Akyüz, Melanie Goisauf, Gillian M Martin, et al.Translational Lung Cancer Research|July 17, 2025
Monitoring pembrolizumab response in patients with metastatic non-small cell lung cancer using circulating tumour DNA and circulating tumour cellsAndrea C Kakouri, Maria Spiliotaki, Eleni M Loizidou, et al.Journal of the American Society of Nephrology : JASN|October 19, 2007
COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathyKonstantinos Voskarides, Loukas Damianou, Vassos Neocleous, et al.BMC Nephrology|May 17, 2018
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi, et al.Gene|February 15, 2015
Haploinsufficiency of the miR-873/miR-876 microRNA cluster is associated with craniofacial abnormalitiesCostas Koufaris, Gregoris Papagregoriou, Ludmila Kousoulidou, et al.Glomerular Diseases|June 10, 2025
Familial Kidney Disease Phenocopying Hypertensive NephropathyFezile Ozdemir, D Deren Oygar, Ahmet Behlul, et al.Pediatric Nephrology (Berlin, Germany)|May 31, 2013
DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome, Judy Savige, Elisabet Ars, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 10, 2009
Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosisAlkis Pierides, Konstantinos Voskarides, Yiannis Athanasiou, et al.Pageof 9