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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 11, 2003
Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuriaFaysal Gok, Kimiyoshi Ichida, Rezan TopalogluOphthalmic Genetics|January 13, 2016
An Unusual Cause of Pseudopapillary Oedema: Hyperphosphatemic Hyperostosis SyndromeErhan Yumusak, Fatih Mehmet Mutlu, Faysal GokRheumatology International|August 19, 2007
Pathogenesis-related adhesion molecules in Henoch-Schonlein vasculitisFaysal Gok, Yesim Ugur, Seza Ozen, et al.Pediatric Nephrology (Berlin, Germany)|May 1, 2008
Oral-ibuprofen-induced acute renal failure in a preterm infantOmer Erdeve, S Umit Sarici, Erkan Sari, et al.Acta Orthopaedica|March 21, 2009
Newly discovered mutations in the GALNT3 gene causing autosomal recessive hyperostosis-hyperphosphatemia syndromeFaysal Gok, Ilana Chefetz, Margarita Indelman, et al.Clinical Rheumatology|November 15, 2007
A very frequent mutation and remarkable association of R761H with M694V mutations in Turkish familial Mediterranean fever patientsErkan Demirkaya, Yusuf Tunca, Faysal Gok, et al.Case Reports in Rheumatology|February 19, 2015
A new mutation in blau syndromeCengiz Zeybek, Gokalp Basbozkurt, Davut Gul, et al.Pediatric Nephrology (Berlin, Germany)|February 24, 2006
Ceftriaxone-related hemolysis and acute renal failureErkan Demirkaya, Abdullah Avni Atay, Ugur Musabak, et al.Pediatric Nephrology (Berlin, Germany)|June 14, 2013
QT and JT dispersion and cardiac performance in children with neonatal Bartter syndrome: a pilot studyDuygu Ovunc Hacihamdioglu, Kursat Fidanci, Ayhan Kilic, et al.Pediatric Neurology|November 1, 2006
Increased intracranial pressure due to chronic active Epstein-Barr virus infectionAyhan Dagdemir, Haydar Ali Tasdemir, Cengiz Dilber, et al.Pageof 4