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Potential utility of dermoscopy in the examination of ocular pigmentations

Autor: Kaçar, Nida, Yıldırım, Cem, Demirkan, Neşe, Bulgu, Y.

Publikováno v: Dermatology Practical & Conceptual, Vol 8, Iss 3 (2018)
Dermatology Practical & Conceptual

Background: Dermoscopy is a fundamental method in the examination of melanocytic neoplasms. Limited data exist about the dermoscopic features of ocular pigmentations (OPs). Objectives: We aimed to investigate the usefulness of dermoscopy in the exami

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7071b6fcdd373060a9875c2254dd0bb6
https://doi.org/10.5826/dpc.0803a12

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Vascular endothelial growth factor gene polymorphisms in age-related macular degeneration in a Turkish population

Autor: Bulgu, Y, Çetin, Gökhan Ozan, Caner, Vildan, Çetin, Ebru Nevin, Yaylali, V, Yildirim, C

Publikováno v: International Journal of Ophthalmology, Vol 7, Iss 5, Pp 773-777 (2014)

AIM:To assess the association between age-related macular degeneration (AMD) and three single nucleotide polymorphisms (SNPs) related to the vascular endothelial growth factor (VEGF) gene.METHODS: The patients who were diagnosed with AMD were include

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::588e0bec51f18fb2141084fb7aada728
http://www.ijo.cn/en_publish/2014/5/20140506.pdf

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HIF1A as a major vascular endothelial growth factor regulator: do its polymorphisms have an association with age-related macular degeneration?

Autor: Okur V, Cetin O, Cetin E, Tepeli E, Bulgu Y, Yildirim C

BACKGROUND: To investigate the association between age-related macular degeneration (AMD) and the polymorphisms of HIF1A, a major vascular epithelial growth factor regulator under hypoxic conditions. The associations of AMD and polymorphisms of genes

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::e5797d2fe6fe93b15bb49805663988b8

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HIF1A as a major vascular endothelial growth factor regulator: Do its polymorphisms have an association with age-related macular degeneration?

Autor: Okur, Volkan., Çetin, Ozan, Çetin, Ebru, Tepeli, E., Bulgu, Y., Yildirim, C.

Background: To investigate the association between age-related macular degeneration (AMD) and the polymorphisms of HIF1A, a major vascular epithelial growth factor regulator under hypoxic conditions. The associations of AMD and polymorphisms of genes

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4539bcac27f8c9a138d367b99db7b52f
https://hdl.handle.net/11499/10294

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HIF1A as a major vascular endothelial growth factor regulator: do its

Autor: Okur, V, Cetin, O, Cetin, E, Tepeli, E, Bulgu, Y, Yildirim, C

BackgroundTo investigate the association between age-related macular degeneration (AMD) and the polymorphisms of HIF1A, a major vascular epithelial growth factor regulator under hypoxic conditions. The associations of AMD and polymorphisms of genes C

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a95ef1e5eca5327c3b7029dfc91158a0
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/15220

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Vascular endothelial growth factor gene polymorphisms in age-related

Autor: Bulgu, Y, Cetin, GO, Caner, V, Cetin, EN, Yaylali, V, Yildirim, C

AIM: To assess the association between age-related macular degeneration (AMD) and three single nucleotide polymorphisms (SNPs) related to the vascular endothelial growth factor (VEGF) gene.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::620e83257fef266f4de98ab62737c21d
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/14348

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Novel splice-site and missense mutations in the ALDH1A3 gene underlying autosomal recessive anophthalmia/microphthalmia

Autor: Semerci CN, Kalay E, Yıldırım C, Dinçer T, Olmez A, Toraman B, Koçyiğit A, Bulgu Y, Okur V, Satıroğlu-Tufan L, Akarsu NA

AIM: This study aimed to identify the underlying genetic defect responsible for anophthalmia/microphthalmia. METHODS: In total, two Turkish families with a total of nine affected individuals were included in the study. Affymetrix 250 K single nucleot

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::18e7fff6a6d20db78509de96c1ef199a

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autosomal recessive anophthalmia/microphthalmia

Autor: Semerci, CN, Kalay, E, Yildirim, C, Dincer, T, Olmez, A, Toraman, B, Kocyigit, A, Bulgu, Y, Okur, V, Satiroglu-Tufan, L, Akarsu, NA

Aim This study aimed to identify the underlying genetic defect responsible for anophthalmia/microphthalmia. Methods In total, two Turkish families with a total of nine affected individuals were included in the study. Affymetrix 250 K single nucleotid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1aff6441feb6fbb06c94b510208327d8
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/14517

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Vascular endothelial growth factor gene polymorphisms in age-related macular degeneration in a Turkish population

Autor: Bulgu Y, Cetin GO, Caner V, Cetin EN, Yaylali V, Yildirim C

AIM: To assess the association between age-related macular degeneration (AMD) and three single nucleotide polymorphisms (SNPs) related to the vascular endothelial growth factor (VEGF) gene. METHODS: The patients who were diagnosed with AMD were inclu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::6bc99c6eaf5972ba30aa52e1e445e0ba

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Association of serum lipid levels with diabetic retinopathy

Autor: Cetin EN, Bulgu Y, Ozdemir S, Topsakal S, Akın F, Aybek H, Yıldırım C

AIM: To assess the association between serum lipids and diabetic retinopathy (DR). METHODS: Sixty-one diabetic patients without retinopathy(NDR), 55 diabetic patients with non-proliferative retinopathy(NPDR) and 75 diabetic patients with proliferativ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::428faa89c0bbca79674b888f487b4d95

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