Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Mehmet C Mocan"'
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 13, Iss 4, Pp 417-424 (2023)
Axenfeld–Rieger syndrome (ARS) is a rare autosomal-dominant neurocristopathy that presents with a variety of classical ocular and systemic findings. The pathophysiology of the disease involves anterior segment dysgenesis, and patients may present w
Externí odkaz:
https://doaj.org/article/1213c5c4cfc24ad2bb7005b00de94c91
Publikováno v:
Indian Journal of Ophthalmology, Vol 63, Iss 1, Pp 15-19 (2015)
Purpose: To evaluate whether prostaglandin (PG) analogue use is associated with alterations in keratocyte density and central corneal thickness (CCT) in subjects with primary open-angle glaucoma (POAG). Materials and Methods: Thirty-five POAG patient
Externí odkaz:
https://doaj.org/article/5a8533d0c93b4c6c9d2e96ba433ddb44
Autor:
Sibel Kocabeyoglu, Mehmet C Mocan, Ibrahim C Haznedaroglu, Aysegul Uner, Enes Uzunosmanoglu, Murat Irkec
Publikováno v:
Indian Journal of Ophthalmology, Vol 62, Iss 9, Pp 938-940 (2014)
In this paper, we report two cases of a 62-year-old patient presented with blurred vision and a 45-year-old male diagnosed with multiple myeloma who was referred from the Department of Oncology. Slit-lamp examination, in vivo confocal microscopy (IVC
Externí odkaz:
https://doaj.org/article/4f99b8c14ace4728b5e87f97989ba2c1
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 25, Iss , Pp 101406- (2022)
Purpose: The purpose of this case report is to describe the increased fragility of anterior capsule in patients with the rare genetic disease Marshall-Stickler syndrome. Observations: We describe a 3-year old patient with Marshall-Stickler Syndrome a
Externí odkaz:
https://doaj.org/article/660ccda119114f6bbb4e82793cee96e1
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 49, Iss 6, Pp 347-355 (2019)
Primary congenital glaucoma (PCG) continues to be an important cause of visual impairment in children despite advances in medical and surgical treatment options. The progressive and blinding nature of the disease, together with the long lifespan of t
Externí odkaz:
https://doaj.org/article/8bdfe7d3705149799688812d21996479
Autor:
Samuel Cubillos, Mehmet C. Mocan
Publikováno v:
Journal of Pediatric Ophthalmology & Strabismus. 60
The visual outcomes of seven children with specific optic nerve pathologies and coexisting amblyopia after at least 1 year of part-time patching demonstrated a visual acuity improvement of greater than 0.1 logMAR. The results suggest that part-time p
Autor:
Demet Yabanoglu, Figen Soylemezoglu, Mehmet C. Mocan, Özlem Tanas Işıkcı, Murat Irkec, Mehmet Orhan
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 51, Iss 4, Pp 246-249 (2021)
Turkish Journal of Ophthalmology
Turkish Journal of Ophthalmology
Spheroidal corneal degeneration is predominantly seen in advanced age and hereditary predisposition to this disorder is very rare. This report describes the occurrence of bilateral band-shaped spheroidal corneal degeneration in two siblings.
Publikováno v:
Clinical Ophthalmology (Auckland, N.Z.)
Samiksha Fouzdar-Jain,1 Zena Ibrahim,2 Jeremy Reitinger,3 Dingcai Cao,2 Mehmet C Mocan2 1Department of Pediatric Ophthalmology & Adult Strabismus, Children’s Hospital and Medical Center, Omaha, NE, USA; 2Department of Ophthalmology and Visual Scien
Publikováno v:
Current Eye Research. 46:796-801
Purpose: To investigate the association between meibomian gland (MG) loss and corneal subbasal nerve plexus density in patients with chronic graft-versus-host disease (GVHD) related dry eye disease...
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 26:e27-e28