Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Gulunay Kiray"'
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 7, Iss 6, Pp 579-584 (2020)
OBJECTIVE: To evaluate the results and recurrence rates of external and endonasal dacryocystorhinostomy (DCR) surgery in patients with primary acquired nasolacrimal duct obstruction (PANDO) in Turkish Cohort. METHODS: Medical records were reviewed in
Externí odkaz:
https://doaj.org/article/f18db56315e64299ae185ce468fa6503
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 18, Iss , Pp - (2020)
Purpose: To describe the phenotypic and genotypic characteristics of two families with cone dystrophy with supernormal rod responses (CDSRR) presenting with a pseudodominant inheritance of disease. Observations: Three affected members from each famil
Externí odkaz:
https://doaj.org/article/7ab5dfc62d504dc3bffa41383137849e
Publikováno v:
Ophthalmic genetics. 43(5)
Harboyan syndrome is a rare autosomal recessive disorder characterised by congenital hereditary endothelial dystrophy (CHED), with a later onset of sensorineural hearing loss, due to pathogenic variants in the
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184:708-717
Inherited retinal diseases are clinically heterogeneous and are associated with nearly 300 different genes. In this retrospective, observational study of a consecutive cohort of 159 patients (134 families) with childhood-onset (
Autor:
Esra Kardes, Emin Pala, Betül Ayaz, Gülay Karakuş Hacıoğlu, Gulunay Kiray, Betul Ilkay Sezgin Akcay
Publikováno v:
International Ophthalmology
Purpose Evaluation of subtle ocular involvement and clinically significant conjunctivitis symptoms in a group of patients with COVID-19 in outpatient and inpatient settings. Method Overall, 1083 patients infected with SARS-CoV-2 were recruited as sub