Prof.Dr. E.Cumhur ŞENER | Göz Hastalıkları Uzmanı
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Superior or inferior rectus transposition in esotropic Duane syndrome: a longitudinal analysis.
Botulinum toxin-A injection in esotropic Duane syndrome patients up to 2 years of age.
Strabismus surgery in congenital fibrosis of the extraocular muscles: a paradigm.
Ocular Causes of Abnormal Head Position: Strabismus Clinic Data.
Inferior Rectus Transposition a Novel Procedure for Abducens Palsy.
Effect of Visual Acuity on the Surgical Outcomes of Secondary Sensory Strabismus.
Clinical risk factors for the development of consecutive exotropia: a comparative clinical study.
Horizontal muscle transposition or oblique muscle weakening for the correction of V pattern?
Functional Amblyopia and Deficient Binocular Vision as Initial Clinical Features in Duane's Syndrome.
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development.
Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).
Ocular motility disturbances after episcleral plaque brachytherapy for uveal melanoma.
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).

https://www.ncbi.nlm.nih.gov/pubmed/14595441

Right-sided Duane retraction syndrome associated with multiple malformations.
Management of strabismus in nanophthalmic patients: a long-term follow-up report.

https://www.ncbi.nlm.nih.gov/pubmed/12799252

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development
Superior oblique surgery: when and how?
Bilateral choroidal detachment following cataract surgery in a 40-day-old infant.
Late correction for blow-out sequelae: transposition of a longitudinally transected inferior rectus muscle.

https://www.ncbi.nlm.nih.gov/pubmed/23703703

Amblyopia and sensory features at initial presentation of Brown syndrome: an issue to recognize.
Inferior oblique muscle weakening: is it possible to quantify its effects on horizontal deviations?
Sequential presentation of bilateral Brown syndrome.
An assessment of ocular morbidities of children born prematurely in early childhood.
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.
Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia.

https://www.ncbi.nlm.nih.gov/pubmed/18521937

Pediatric ophthalmology and strabismus in Turkey.
The reliability of grading the fixation preference test for the assessment of interocular visual acuity differences in patients with strabismus.
Outcome of abducens nerve paralysis in patients with nasopharyngeal carcinoma.
A multidisciplinary approach to the management of individuals with fragile X syndrome.

https://www.ncbi.nlm.nih.gov/pubmed/17217479

Unrecognized side effect of statin treatment: unilateral blepharoptosis.

https://www.ncbi.nlm.nih.gov/pubmed/16714939

Angle closure glaucoma induced by ritodrine.

https://www.ncbi.nlm.nih.gov/pubmed/15842216

Factors affecting the antibacterial effects of Nd:YAG laser in vivo.

https://www.ncbi.nlm.nih.gov/pubmed/12605426

Renal vascular abnormalities in Bardet-Biedl syndrome.

https://www.ncbi.nlm.nih.gov/pubmed/10603122

Ultrastructure of the lens epithelium in Alport's syndrome.

https://www.ncbi.nlm.nih.gov/pubmed/9838255

Congenital Brown's syndrome: clinical and surgical approach.

https://www.ncbi.nlm.nih.gov/pubmed/7819728

Bronchial asthma in a patient with Usher syndrome: case report.

https://www.ncbi.nlm.nih.gov/pubmed/7961327

Punctate inner choroidopathy and its differential diagnosis.

https://www.ncbi.nlm.nih.gov/pubmed/2064259

Etiology of Fourth and Sixth Nerve Palsies: a Single Ophthalmology Clinic’s Perspective