Prof.Dr. E. Cumhur Şener
Prof.Dr. E. Cumhur ŞENER
Göz Hastalıkları Uzmanı
ulaşım
haber

Yayınlar

 Yayınlardan Bazıları - Selected publications


1.     Sekeroğlu HT, Türkçüoğlu P, Sanaç AŞ, Sener EC. Sequential presentation of bilateral Brown syndrome. J AAPOS. 2012 Apr;16(2):210-2.

2.     Goktas A, Sener EC, Sanac AS. An Assessment of Ocular Morbidities of Children Born Prematurely in Early Childhood. J Pediatr Ophthalmol Strabismus. 2012 Feb 14:1-6.

3.     Tischfield MA, Baris HN, Wu C, Rudolph G, Van Maldergem L, He W, Chan WM, Andrews C, Demer JL, Robertson RL, Mackey DA, Ruddle JB, Bird TD, Gottlob I, Pieh C, Traboulsi EI, Pomeroy SL, Hunter DG, Soul JS, Newlin A, Sabol LJ, Doherty EJ, de Uzcátegui CE, de Uzcátegui N, Collins ML,Sener EC, Wabbels B, Hellebrand H, Meitinger T, de Berardinis T, Magli A, Schiavi C, Pastore-Trossello M, Koc F, Wong AM, Levin AV, Geraghty MT, Descartes M, Flaherty M, Jamieson RV, Møller HU, Meuthen I, Callen DF, Kerwin J, Lindsay S, Meindl A, Gupta ML Jr, Pellman D, Engle EC. Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. Cell. 2010 Jan 8;140(1):74-87

4.     Chang B, Grau T, Dangel S, Hurd R, Jurklies B, Sener EC, Andreasson S, Dollfus H, Baumann B, Bolz S, Artemyev N, Kohl S, Heckenlively J, Wissinger B. A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene. Proc Natl Acad Sci U S A. 2009 Nov 17;106(46):19581-6.

5.     Reuter P, Koeppen K, Ladewig T, Kohl S, Baumann B, Wissinger B; Achromatopsia Clinical Study Group. Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia. Hum Mutat. 2008 Oct;29(10):1228-36.

6.     Alanay Y, Unal F, Turanli G, Alikaşifoğlu M, Alehan D, Akyol U, Belgin E, Sener C, Aktaş D, Boduroğlu K, Utine E, Volkan-Salanci B, Ozusta S, Genç A, Başar F, Sevinç S, Tunçbilek E. A multidisciplinary approach to the management of individuals with fragile X syndrome. J Intellect Disabil Res. 2007 Feb;51(Pt 2):151-61.

7.     Ertas FS, Ertaş NM, Gulec S, Atmaca Y, Tanju S, Sener C, Erol C. Unrecognized side effect of statin treatment: unilateral blepharoptosis. Ophthal Plast Reconstr Surg. 2006 May-Jun;22(3):222-4.

8.     Sanaç AS, Sener EC. Pediatric ophthalmology and strabismus in Turkey. J AAPOS. 2006 Apr;10(2):100-1.

9.     Tischfield MA, Bosley TM, Salih MA, Alorainy IA, Sener EC, Nester MJ, Oystreck DT, Chan WM, Andrews C, Erickson RP, Engle EC. Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Nat Genet. 2005 Oct;37(10):1035-7.

10.  Guvendag Guven ES, Guven S, Coskun F, Ayhan A, Sener C. Angle closure glaucoma induced by ritodrine. Acta Obstet Gynecol Scand. 2005 May;84(5):489-90.

11.  Yamada K, Chan WM, Andrews C, Bosley TM, Sener EC, Zwaan JT, Mullaney PB, Oztürk BT, Akarsu AN, Sabol LJ, Demer JL, Sullivan TJ, Gottlob I, Roggenkäemper P, Mackey DA, De Uzcategui CE, Uzcategui N, Ben-Zeev B, Traboulsi EI, Magli A, de Berardinis T, Gagliardi V, Awasthi-Patney S, Vogel MC, Rizzo JF 3rd, Engle EC. Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3). Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2218-23.

12.  Sener EC, Kiratli H, Gedik S, Sanac AS. Ocular motility disturbances after episcleral plaque brachytherapy for uveal melanoma. J AAPOS. 2004 Feb;8(1):38-45.

13.  Yamada K, Andrews C, Chan WM, McKeown CA, Magli A, de Berardinis T, Loewenstein A, Lazar M, O'Keefe M, Letson R, London A, Ruttum M, Matsumoto N, Saito N, Morris L, Del Monte M, Johnson RH, Uyama E, Houtman WA, de Vries B, Carlow TJ, Hart BL, Krawiecki N, Shoffner J, Vogel MC, Katowitz J, Goldstein SM, Levin AV, Sener EC, Ozturk BT, Akarsu AN, Brodsky MC, Hanisch F, Cruse RP, Zubcov AA, Robb RM, Roggenkäemper P, Gottlob I, Kowal L, Battu R, Traboulsi EI, Franceschini P, Newlin A, Demer JL, Engle EC. Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). Nat Genet. 2003 Dec;35(4):318-21.

14.  Yalcin SS, Cagdas D, Şener EC, Yurdakok M. Right-sided Duane retraction syndrome associated with multiple malformations. Pediatr Int. 2003 Oct;45(5):577-9.

15.  Şener EC, Mocan MC, Sarac OI, Gedik Ş, Sanaç AŞ. Management of strabismus in nanophthalmic patients: a long-term follow-up report. Ophthalmology. 110:1230-6, 2003.

16.  Şener EC, Mocan MC, Gedik Ş, Ergin A, Sanaç AŞ. The reliability of grading the fixation preference test for the assessment of interocular visual acuity differences in patients with strabismus. J AAPOS 6: 191-4, 2002.

17.  Tomaç S, Şener EC, Sanaç AŞ. Clinical and sensorial characteristics of microtropia. Japanese J Ophthalmol 46: 52-8, 2002.

18.  İlhan Ö, Şener EC, Özyar E. The outcome of abducens nerve paralysis in patients with nasopharyngeal carcinoma. Eur J Ophthalmol 12: 55-9, 2002.

19.  Nakano M, Yamada K, Fain J, Şener EC, Selleck CJ, Awad AH, Zwaan J, Mullaney PB, Bosley TM, Engle CE. Homozygous mutations in ARIX result in congenital fibrosis of the extraocular muscles type 2. Nature Genetics 29: 1-6, 2001.

20.  Şener EC, Önerci M. Reappraisal of probing of the congenital obstruction of the nasolacrimal system: is nasal endoscopy essential? Int  J Pediatric Otorhinolaryngology 58: 65-8, 2001.

21.  Wissinger B, Gamer D, Jaegle H, Giorda R, Marx T, Mayer S, Tippmann S, Broghammer M, Jurklics B, Rosenberg T, Jacobson SG, Şener EC, Tatlıpınar S, Hoyng CB, Castellan C, Bitoun P, Andreasson S, Rudolph G, Kellner U, Lorenz B, Wolff G, Verellen-Dumoulin C, Schwartz M, Cremers FPM, Apfellstedt-Sylla E, Zrenner E, Salati R, Sharpe LT, Kohl S. CNGA3 mutations in hereditary cone photoreceptor disorders. Am J Hum Genet 69: 722-37, 2001. (presented at the Association of Human Genetics, San Fransisco 1999, Am J Hum Genet 65: A498, 1999)

22.  Tatlıpınar S, Şener EC, İlhan B, Semerci B. Ophthalmic manifestations of Gilles de la Tourette syndrome. Eur J Ophthalmol 11: 223-6, 2001.

23.  Kadayıfçılar S, Özatlı D, Özcebe Oİ, Şener EC. Is activated factor VII associated with retinal vein occlusion? Br J Ophthalmol 85: 1174-8, 2001.

24.  Oruç S, Şener EC, Akman A, Sanaç AŞ. Bilateral orbital hemorrhage induced by labor. Eur J Ophthalmol 11: 77-9, 2001.

25.  Şener EC, Kıratlı H. Presumed sertraline maculopathy. Acta Ohthalmol Scand 79: 428-30, 2001.

26.  Şener EC, Lee BJ, Turgut B, Akarsu AN, Engle EC. A clinically variant fibrosis syndrome in a Turkish family maps to the CFEOM 1 locus on chromosome 12. Arch Ophthalmol 118: 1090-7, 2000.

27.  Şener EC, Sanaç AŞ. Efficacy and complications of dose increments of botulinum toxin-A in the treatment of horizontal comitant strabismus. Eye 14: 873-8, 2000.

28.  Oruç S, Şener EC. A comparative study of the effects of aproclonidine and timolol on the ophthalmic blood flow velocity waveforms. Int Ophthalmol 23: 69-73, 1999.

29.  Engle EC, Lee BA, Şener EC, Turgut B, Akarsu N, Khamis AR, Mousawi A, Traboulsi EI. Phenotypic variation at the chromosome 12 CFEOM-1. Am J Hum Genet 65: A248, 1999 (presented at the  Association of Human Genetics, San Fransisco 1999).

30.  Akarsu AN, Şener EC, Keçeci A, Özbaş F, Sotirova V, Sarfarazi M, Özgüç M. Ascertainment of large strabismus families and mapping of the first locus to the short arm of X chromosome. Invest Ophthalmol Vis Sci 39: 908, 1998. (presented at the Association of Resarch in Vision and Ophthalmology Meeting ARVO, Florida 1998)

31.  Sargon MF, Çelik H, Şener EC. Ultrastructure of the lens epithelium in Alport’s syndrome. Ophthalmologica 213: 30-3, 1999.

32.  Şener EC, Çalışkan S. Ophthalmology and molecular genetics. Ophthalmology- Medical Network 5: 103-6, 1998. (English abstract)

33.  Öndeş S, Nurlu G, İlhan B, Şener EC, Sanaç AŞ. The effect of levodopa on visual evoked potentials in anisometropic amblyopia. Türkiye Klinikleri J Ophthalmol 7: 92-5, 1998 (English Abstract)

34.  Şener EC, Özerdem U, İrkeç M, Sanaç AŞ. Long term results of trabeculectomy with mitomycin-C and releasable suture application. Ophthalmology-Medical Network 5: 21-3,1998. (English abstract)

35.  Şener EC, Öndeş S, Önerci M, Sanaç AŞ. Thyroid ophthalmopathy and endoscopic decompression. Ophthalmology-Medical Network 5: 65-8,1998. (English abstract)

36.  Simons K, Stein L, Şener EC, Vitale S, Guyton DL. Full-time atropine, intermittent atropine, and optical penalization and binocular outcome in treatment of strabismic amblyopia. Ophthalmology  12: 2143-55, 1997.

37.  Özkan SB, Arıbal ME, Şener EC, Sanaç AŞ, Gürcan S. Magnetic resonance imaging in evaluation of congenital and acquired superior oblique palsy. J Pediatric Ophthalmol Strabismus 34: 29-34, 1997 (Presented in part at the European Strabismological Association 24th Meeting, 1996)

38.  Şener EC. Anatomy and physiology of extraocular muscles, eye movements, and binocular vision. Ophthalmology-Medical Network (Strabismus Special Issue) 4: 380-5, 1997 (Invited manuscript, Turkish)

39.  İlhan B, Şener EC, Oruç S, Akman A, Babuccu S, Sanaç AŞ. Clinical features of strabismus patients. Türkiye Klinikleri J Ophthalmol 6: 115-119, 1997 (English Abstract)

40.  Şener EC, Özkan SB, Arıbal ME, Sanaç AŞ, Aslan B. Evaluation of congenital Brown’s syndrome with magnetic resonance imaging. Eye 10: 492-496, 1996 

41.  Abbasoğlu ÖE, Şener EC, Sanaç AŞ. Factors influencing success and dose effect relation of botulinum A treatment. Eye 10: 385-391, 1996

42.  Abbasoğlu ÖE, Şener EC, Sanaç AŞ. Factors influencing the successful outcome and response in strabismus surgery. Eye 10: 315-320, 1996

43.  Akman A, Dayanır V, Şener EC, Sanaç AŞ. Acquired Duane’s retraction syndrome. J Pediatric Ophthalmol and Strabismus 33: 267-269, 1996

44.  Akman A, Dayanır V, Şener EC, Sanaç AŞ. Acquired Duane’s retraction syndrome. J Pediatric Ophthalmol and Strabismus 34: 76-7, 1997

45.  Çakmak HB, Toprak AB, Özerdem U, Şener EC, Kansu T, Sanaç AŞ. Etiology in paralytic strabismus cases.  Turkish Ophthalmological Association 30th National Congress Bulletin, 1996 (English abstract)

46.  Toprak AB, Çakmak HB, Dursun D, Şener EC, Sanaç AŞ. Clinical features and surgical results of infantile esotropia. Turkish Ophthalmological Association 30th National Congress Bulletin, 1996 (English abstract)

47.  İlhan B, Şener EC, Oruç S, Akman A, Babuccu S, Sanaç AŞ. Clinical features of strabismus cases. Türkiye Klinikleri J Ophthalmol 6: 160-4, 1996 (English Abstract)

48.  Şener EC, Yıldırım C, Sanaç AŞ, Guyton DL. Inferior oblique disinsertion: effect on horizontal alignment in primary position. Binocular Vision and Eye Muscle Surgery Quarterly 10: 233-242, 1995. (Presented at the American Academy of Ophthalmology Meeting, San Fransisco 1994)

49.  Eldem B, Abbasoglu ÖE, Sener EC. Capillary hemangioma of the optic disc. Annals of Ophthalmology and Glaucoma 27: 212-216, 1995. (cited in full text at the Mosby Year Book of Ophthalmology 1996)

50.  Şener EC, Bilgiç S, Çalışkan S. Maxillary osteomyelitis in early infancy. Turkish Journal of Medical Sciences 24: 327-329, 1995.

51.  Berk AT, Erkan D, Şener EC, Sanaç AŞ. Congenital Brown’s syndrome: clinical and surgical approach. European J Ophthalmol 4: 138-143, 1994

52.  Şener EC, Dayanır V, Oruç S, Sanaç AŞ, Akalın S, Turan E. Management of thyroid ophthalmopathy. Türkiye Klinikleri J Ophthalmol 3: 260-267, 1994 (English Abstract)

53.  Barış B, Ataman M, Şener EC, Kalyoncu F. Bronchial asthma in a patient with Usher syndrome: Case report. Journal of Asthma. 31: 487-490, 1994.

54.  Şener EC, Özkan SB, Çuhadaroğlu H, Orhan M, Erdener U, Sanaç AŞ.  Botulinum toxin therapy in amblyopic and or previously operated patients. Transactions 20th Meeting European Strabismological Association, H. Kaufmann (ed), 1992, Brussels, pp 357-360.

55.  Özkan SB, Orhan M, Şener EC, Sanaç AŞ, Duman S, Berk T. Binocular function and vertical deviations in infantile esotropia following early surgery. Transactions 20th. Meeting European Strabismological Association, H. Kaufmann (ed), Brussels, p: 173-178, 1992.

56.  Sanaç AŞ, Kutluk S, Özkan SB, Şener EC, Erkan D, Erdener U. The results of faden operation in congenital nystagmus dampening by convergence. Transactions 20th. Meeting European Strabismological Association, H. Kaufmann (ed), Brussels, s: 361-364, 1992.

57.  Eldem B, Şener EC. Punctate inner choroidopathy and its differential diagnosis. Annals of Ophthalmology. 23: 153-155, 1991.