Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Panel-based next-generation sequencing identifies novel mutations in Bulgarian patients with inherited retinal dystrophies.
Mol Genet Genomic Med. 2022 Aug;10(8):e1997. doi: 10.1002/mgg3.1997. Epub 2022 Jun 3.
Mol Genet Genomic Med. 2022.
PMID: 35656873
Free PMC article.
A rare case of RGR/CDHR1 haplotype identified in Bulgarian patient with cone-rod dystrophy.
Mermeklieva E, Kamenarova K, Mihova K, Shakola F, Kaneva R.
Mermeklieva E, et al.
Ophthalmic Genet. 2021 Dec;42(6):747-752. doi: 10.1080/13816810.2021.1946700. Epub 2021 Jul 6.
Ophthalmic Genet. 2021.
PMID: 34229535
Item in Clipboard
Reference values of pattern reversal visual evoked potentials in Bulgarian population.
Mermeklieva EA.
Mermeklieva EA.
Eur J Ophthalmol. 2019 Nov;29(6):600-605. doi: 10.1177/1120672118802545. Epub 2018 Sep 24.
Eur J Ophthalmol. 2019.
PMID: 30246542
Item in Clipboard
Pattern electroretinography and retinal changes in patients with diabetes mellitus type 2.
Mermeklieva EA.
Mermeklieva EA.
Neurophysiol Clin. 2019 Jun;49(3):209-215. doi: 10.1016/j.neucli.2019.04.002. Epub 2019 May 11.
Neurophysiol Clin. 2019.
PMID: 31088708
Item in Clipboard
Cite
Cite