OpenAlex konusu

Ocular Disorders and Treatments

Bu sayfa OpenAlex konu etiketine göre çalışmaları ve o konuda görünen akademisyenleri listeler. YÖKSİS temel alan / yan dal değildir.

OpenAlex 1.291 eser 15 yazar konusu

Çalışmalar

1.291 eser

Assignment of a Locus GLC3A for Primary Congenital Glaucoma Buphthalmos to 2p21 and Evidence for Genetic Heterogeneity 1995
YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.3%
Özet henüz yok.
- AYŞE NURTEN AKARSU
Effect of Surface Treatments and Coffee Thermocycling on the Color and Translucency of CAD-CAM Monolithic Glass-Ceramic 2018
YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.4%
Özet henüz yok.
- MERYEM GÜLCE SUBAŞI
The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries 2022
YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.9%
BACKGROUND: Retinoblastoma is the most common intraocular cancer worldwide. There is some evidence to suggest that major differences exist in treatment outcomes for children with retinoblastoma from different regions, but these differences have not been assessed on a global scale. We aimed to report 3-year outcomes fo…
- HATİCE TUBA ATALAY
- MEHMET KANTAR
The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries 2022
YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.9%
BACKGROUND: Retinoblastoma is the most common intraocular cancer worldwide. There is some evidence to suggest that major differences exist in treatment outcomes for children with retinoblastoma from different regions, but these differences have not been assessed on a global scale. We aimed to report 3-year outcomes fo…
- MEHMET KANTAR
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development 2017
OpenAlex üst %10 OpenAlex 97.8%
Özet henüz yok.
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development 2017
YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 97.8%
Özet henüz yok.
- HÜLYA KAYSERİLİ KARABEY
SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice 2011
YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 92.6%
Özet henüz yok.
- MUHSİN ÖZGÜR ÇOĞULU
Phenotypic variability in 49 cases of ESCO2 mutations including novel missense and codon deletion in the acetyltransferase domain correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome 2010
YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 93.6%
BACKGROUND: Roberts syndrome (RBS) and SC phocomelia are caused by mutations in ESCO2, which codes for an acetyltransferase involved in the regulation of sister chromatid cohesion. Of 26 mutations described to date, only one missense mutation has been reported and all others are predicted to be truncating mutations. G…
- HÜLYA KAYSERİLİ KARABEY
Color of bulk-fill composite resin restorative materials 2018
YÖKSİS SJR Q1 JCR Q2 OpenAlex üst %10 OpenAlex 94.8%
Abstract Objective To evaluate the color stability of novel bulk‐fill composite resins. Materials and Methods Color measurements of a nanohybrid composite resin (Z550) and 3 bulk‐fill composite resins (BLK, AFX, XTF; n = 45) were performed before polymerization. After polymerization, color measurements were repeated a…
- MEHMET MUSTAFA ÖZARSLAN
Retrospective study of treatment outcomes with implant-retained extraoral prostheses: Survival rates and prosthetic complications 2010
OpenAlex üst %10 OpenAlex 93.8%
Özet henüz yok.
Management of glaucoma in patients with nanophthalmos 2007
OpenAlex 80.9%
Özet henüz yok.
Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations 2014
OpenAlex üst %10 OpenAlex 96.5%
Özet henüz yok.

Akademisyenler

15 akademisyen