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Clinical Genetics|April 5, 2024
Beyond the phenotype: Exploring inherited retinal diseases with targeted next-generation sequencing in a Turkish cohortBusra Ozguc Caliskan, Kubra Uslu, Neslihan Sinim Kahraman, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 7, 2007
Ocular blood flow in patients with obstructive sleep apnea syndrome (OSAS)Sarper Karakucuk, Sertan Goktas, Murat Aksu, et al.
The Turkish Journal of Pediatrics|December 31, 2003
Analysis of the modifying effects of SAA1, SAA2 and TNF-alpha gene polymorphisms on development of amyloidosis in FMF patientsEngin Yilmaz, Banu Balci, Sim Kutlay, et al.
The British Journal of Ophthalmology|December 4, 2012
Obstructive sleep apnoea prevalence in non-arteritic anterior ischaemic optic neuropathyHatice Arda, Serife Birer, Murat Aksu, et al.
Renal Failure|July 29, 2008
Long-term efficacy and safety of quadruple therapy in childhood diffuse proliferative lupus nephritisGülay Demircin, Ayse Oner, Ozlem Erdoğan, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 1, 2020
Inherited eye diseases in Turkey: Current approaches and future directionsFulya Yaylacioglu Tuncay, Sezen Guntekin Ergun, Ayse Oner, et al.
Pediatric Nephrology (Berlin, Germany)|March 3, 2011
Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutationEsra Baskin, Umut Selda Bayrakci, Füsun Alehan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 29, 2002
A retrospective analysis for aetiology and clinical findings of 287 secondary amyloidosis cases in TurkeySerhan Tuglular, Fatos Yalcinkaya, Saime Paydas, et al.
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