Zobrazeno 1 - 6
of 6
pro vyhledávání: '"S G, Aktan"'
Publikováno v:
European Journal of Ophthalmology. 5:181-186
Ophthalmic screening was done on 23,810 children visited at schools in different regions of Ankara. Children with below normal visual acuity were invited to the outpatient department and had a full routine ocular examination. Thirty-nine nursery and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a518e6d049a9422fc1d87f2fcbbac5c
https://doi.org/10.1177/112067219500500307
https://doi.org/10.1177/112067219500500307
Autor:
S G, Aktan, R M, Mandelkorn
Publikováno v:
Ophthalmic surgery and lasers. 29(8)
Traditionally, the argon laser has been used with suture lysis. The authors evaluate the krypton laser and define the parameters for the successful use of the laser with this procedure.Five consecutive patients undergoing combined cataract and trabec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ea66d6ebc7b1732d498e93aea4e260b
https://pubmed.ncbi.nlm.nih.gov/9715487
https://pubmed.ncbi.nlm.nih.gov/9715487
Autor:
M E Turacli, M Or, G Brice, Miguel Coca-Prados, S G Aktan, Line Chevrette, R A Lewis, Anne H. Child, Ivaylo Stoilov, I Alozie, A N Akarsu, Magda Barsoum-Homsy, Mansoor Sarfarazi, Nehir Özdemir
PubMedID: 9497261 We recently reported three truncating mutations of the cytochrome P4501B1 gene (CYP1B1) in five families with primary congenital glaucoma (PCG) linked to the GLC3A locus on chromosome 2p21. This could be the first direct evidence su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f2db4b100f37152222081de0ec0e390
https://avesis.gazi.edu.tr/publication/details/9dbf4e30-6ee3-41a3-9035-c37d2b2d629f/oai
https://avesis.gazi.edu.tr/publication/details/9dbf4e30-6ee3-41a3-9035-c37d2b2d629f/oai
Autor:
A N, Akarsu, M E, Turacli, S G, Aktan, A, Hossain, M, Barsoum-Homsy, L, Chevrette, B S, Sayli, M, Sarfarazi
Publikováno v:
American journal of medical genetics. 61(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::30fe5d3dc874482d5790d201499d4431
https://pubmed.ncbi.nlm.nih.gov/8741877
https://pubmed.ncbi.nlm.nih.gov/8741877
Autor:
A Hossain, Magda Barsoum-Homsy, Line Chevrette, B S Sayli, Mansoor Sarfarazi, S G Aktan, M E Turacli, A N Akarsu
Publikováno v:
Genomics. 30(2)
Primary congenital glaucoma (GLC3) is an inherited eye disorder that accounts for 0.01-0.04% of total blindness. Although a large number of chromosomal abnormalities have already been reported in patients with congenital glaucoma, the precise locatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::606a4386278a47e15268170ff57dee10
https://pubmed.ncbi.nlm.nih.gov/8586416
https://pubmed.ncbi.nlm.nih.gov/8586416
Publikováno v:
International ophthalmology. 16(4-5)
Therapy for congenital glaucoma is primarily surgical. We have investigated 249 cases who have undergone trabeculectomy. There was a 79% success rate as regards to control of the IOP. Vision could be saved among the patients who had applied relativel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ade2116066f1a500788524f2ac0b2c9a
https://pubmed.ncbi.nlm.nih.gov/1428571
https://pubmed.ncbi.nlm.nih.gov/1428571